We thank WesternU College of Optometry and the Master of Science in Medical Sciences program at WesternU for their assistance and support. We also thank ZeaVision for their generous support and funding.

All subjects were recruited at a single site, the Western University of Health Sciences. The study was approved by the institutional review board at Western University of Health Sciences, Pomona, California, USA, and conducted in accordance with the tenets of the Declaration of Helsinki. Prior to participation all participants were given a detailed explanation of the study and signed an informed consent form before any standard ophthalmic evaluation was carried out.
1. Participant recruitment
<ol>
	<li>Include participants that are at least 18 years of age and have a visual acuity of 20/40 or better.</li>
	<li>Include participants with clinically insignificant conditions like cataracts, isolated drusen, posterior vitreous detachment, familial drusen in periphery, and peripheral retinal conditions, such as lattice degeneration, or retinal pigment epithelial defects. Ensure that the participants have normal binocularity and that they do not have suppression32.</li>
	<li>Accomplish this by the administration of a suppression test32. This is a crucial step because in the absence of normal binocularity, participants will not be able to recognize the fixation target and measurement of light source simultaneously and thus would confirm the appropriate location of measurement in the fovea and parafoveal regions.</li>
	<li>Exclude all participants less than 18 years of age, with visual acuity worse than 20/40, with retinal damage in the macula region (central part of the retina), glaucoma, diabetic retinopathy, hemorrhage, severe cataract, or vitreous opacities preventing ophthalmic imaging or MPR measurements.</li>
	<li>Exclude participants who are unable to perform the measurements using heterochromatic flicker photometry or reflectometry, those for whom the devices are unable to provide MPOD values, or those with ocular suppression.</li>
</ol>
2. Creating the peripheral track system (Figure 3)
<ol>
	<li>Obtain a slidable track with an approximately 1 m (3.5 feet) long aluminum rail that contains a hollow indent with space for a slidable track, such as a door weather strip.</li>
	<li>Mount the track 6.1 m (20 feet) from the subject seated at the MPR for the reflectometry measurements to be performed. Ensure that the track is 1.5 m off the ground to be at the same height as the participant&#39;s eye during the reflectometry measurement.</li>
	<li>Mount three 1 cm x 1 cm remote controlled LED lights on the slidable track so that the centers of the lights are spaced 10.7 cm away from each other. 
	NOTE: The 10.7 cm signify each degree and was determined because each LED light is 6.1 m away from the participant. The distance of 6.1 m (~20 feet) is the minimum distance to obtain a true optical infinity, but if a track system is created at a further distance, the distance between each LED light would change and a new distance would have to be calculated trigonometrically. (See Table 1). If fewer than 6 m are utilized, pupillary dilation is advisable to minimize the ocular accommodation.</li>
</ol>
3. Measurements using a heterochromatic flicker photometer
NOTE: This step is for additional data collection and is not essential for peripheral measurements using the reflectometer.
<ol>
	<li>Instill artificial tears in both eyes, ask the participant to blink a few times, and patch the eye that is not being tested.</li>
	<li>Explain the procedure to the participant.</li>
	<li>Instruct the participant to look at the central fixation target of the heterochromatic flicker photometer visible through the eyepiece and to press the clicker each time they observe the target flickering. Ensure that the fixation target flickers a total of five times to determine the initial threshold.</li>
	<li>View the results of the initial threshold and remind the participant to click the button each time the central fixation target flickers as the test continues for 45 s to 1 min.</li>
	<li>A graph and MPOD value will appear on the control monitor along with a reliability index. Ensure that &#34;acceptable&#34; is displayed on the reliability index. Repeat the test if results indicate &#34;borderline&#34; or &#34;unacceptable&#34; until an &#34;acceptable&#34; reliability index is obtained.</li>
	<li>Click on the next green arrow that appears on the control monitor once the participant has finished the test to save the results.</li>
</ol>
4. Central measurement procedure using the reflectometer
NOTE: The subsequent steps will lead to the measurement of individual carotenoids. This is performed using the reflectometer. The central measurements need not be performed to measure peripheral measurements with the reflectometer. However, the central measurements are important for clinical use.
<ol>
	<li>Input the participant information into the reflectometer software.</li>
	<li>Click the Run Eye Test tab.</li>
	<li>White Calibration 
	NOTE: This is a pivotal step in the calibration of the spectrometer within the reflectometer device to full spectrum white sample. This is performed once a day when the device is turned on by the technician. A participant is not needed for this step.
	<ol>
		<li>Click the White button next to Calibrate.</li>
		<li>Insert the white calibration tube onto the reflectometer after the message instructing the user to insert the &#34;white calibration tube&#34; is displayed on the screen.</li>
		<li>Click OK once the white calibration tube is inserted to begin the white calibration. Ensure the Black button next to Calibrate has been enabled after the White Calibration Successful message has appeared on the screen.</li>
	</ol>
	</li>
	<li>Black Calibration
	<ol>
		<li>Instill a drop of artificial tears into the participant&#39;s eyes and have them place their chin onto the chin rest.</li>
		<li>Instruct the participant to place their eye close to the eye cup. Using the joystick, gently position the system so the eye cup presses against the participant&#39;s eye socket and blocks the room light from the system.</li>
		<li>Click the Black button to select Calibrate and align the system to the participant&#39;s pupil. Proper alignment is achieved when the pupil is centered in the circle displayed on the touch screen monitor.</li>
		<li>Instruct the participant to adjust the rotating knob on the front of the system to obtain a clear target.</li>
		<li>Click OK once the participant has properly adjusted the system to their vision. The system will automatically carry out a black calibration sequence. Once black calibration has been successfully completed, the Left Eye and Right Eye buttons will be enabled, and a Black Calibration Successful message will appear on the screen.</li>
	</ol>
	</li>
	<li>Start of measurement
	<ol>
		<li>Click the Left Eye or Right Eye button on the screen depending on which eye is being measured.</li>
		<li>Ensure that the system displays the message Align System to Subject&#39;s Eye. Ensure that the system is aligned to the participant&#39;s pupil. Use the joystick to make fine adjustments.</li>
		<li>Click the OK button on the screen to start the MPOD measurement. The measurement time is 30 s. A minimum of 10 s is needed to obtain the parameters/results. A countdown timer will appear on the top of the screen displaying how much time is left for the measurement. Ask the participant to look at the fixation light and encourage them to only blink when necessary.</li>
		<li>Use the joystick during the measurement to ensure the system stays in alignment with the participant&#39;s pupil.</li>
		<li>Ensure the system displays a message stating Measurement Successful once the measurement is completed.</li>
		<li>Click the OK button to finish.</li>
		<li>Repeat steps 4.4&#8211;4.6.6 to test the other eye if needed. The entire process takes about 2&#8211;3 min. 
		NOTE: To repeat the measurement on the same eye wait at least 30 s then repeat steps 4.6&#8211;4.6.6.</li>
	</ol>
	</li>
</ol>
5. Peripheral measurement technique using reflectometer (Figure 3)
NOTE: The untested eye will fixate on a target allowing for placement of the stimulus at various eccentricities from the fovea of the tested eye. This methodology requires normal binocularity to allow for correct positioning of the eye in which the macular pigment optical density is being measured.
<ol>
	<li>Input participant information into the reflectometry software.</li>
	<li>Click the Run Eye Test tab.</li>
	<li>Peripheral track calibration
	<ol>
		<li>After the white and black calibration is performed, press the Left Eye or Right Eye button on the screen depending on which eye is to be measured.</li>
		<li>The system will display a message Align System to the Subject&#39;s Eye. Ensure that the system is aligned to the participant&#39;s pupil. Use the joystick to make fine adjustments.</li>
		<li>Turn on the LED light on the track system that is farthest right to the participant. At this time, the participant should be able to see both the light from inside the reflectometer with their right eye and the red LED light with their left.</li>
		<li>Instruct the participant to direct the trained observer to adjust the peripheral track until they can superimpose both stimuli to the best of their ability. 
		NOTE: There can be variability between participants on how far their superimposed &#34;calibration point&#34; is due to anatomical differences.</li>
	</ol>
	</li>
	<li>Start of measurement
	<ol>
		<li>Turn off the LED light and switch on the next LED light (to the left) to carry out the next 1 degree eccentric measurement. Explain to the participant that they need to look at the new red LED light throughout the entire measurement.</li>
		<li>Click the OK button on the screen to start the MPOD measurement. The measurement time is 30 s. A countdown timer will appear on the top of the screen displaying how much time is left for the measurement. Ask the participant to look at the appropriate red LED light and encourage them to only blink when necessary.</li>
		<li>Use the joystick during the measurement to ensure the system stays in alignment with the participant&#39;s pupil.</li>
		<li>Ensure the system displays a message stating Measurement Successful once the measurement is completed.</li>
		<li>Click the OK button to finish.</li>
		<li>Repeat steps 5.3.1&#8211;5.4.5 to retake a measurement. 
		NOTE: The entire process takes about 2&#8211;3 min. Two measurements are recommended for each degree to allow for the comparison. To repeat measurements at a different retinal eccentricity, change the degree separation in step 4.8.</li>
	</ol>
	</li>
</ol>
6. Analysis (Figure 4)
<ol>
	<li>Make a copy of the file to be analyzed. 
	NOTE: The file analyzed was generated in steps 4.6.6 and 5.4.5. This step is not essential but allows for various analyses performed without altering the original data.</li>
	<li>Open the reflectometry software on the desktop.</li>
	<li>Click Import on the left side of the application and choose the copied file to be opened.</li>
	<li>Click Edit under the Subject Record tab. A new window will open. This will help obtain data from the desired time interval.</li>
	<li>Move the bottom slide bar up from 0 to 10 to eliminate the first 10 s of measurement. 
	NOTE: The slide bar should read 10&#8211;30. These slide bars can move up or down to choose the desired time interval to analyze. (see Figure 4).</li>
	<li>Click the Exit button on the left side of this window. A warning window will pop up. Select OK to confirm the interval cuts.</li>
	<li>Click Launch Analyzer on the bottom left of the program (see Table of Materials). A new window will open.</li>
	<li>Click Best Fit at the bottom of the page. This will populate the first set of data, including L-OD and Z-OD.</li>
	<li>Record the data.</li>
	<li>Click Reset to select another analysis option.</li>
	<li>Select Macular Pigment under the Receptor Model options.</li>
	<li>Click Best Fit to populate the second set of data, including MPOD.</li>
	<li>Click Save Solution to save this interval.</li>
</ol>

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Dr. Pinakin Davey is a consultant for ZeaVision and Dr. Dennis Gierhart is an Employee, Chief Scientific Officer ZeaVision manufacturer of MPR device. Other authors report no conflicts.

Our study illustrates the technique and methodology to perform in vivo MPOD measurements at various foveal and parafoveal regions using a reflectometer device. We developed and calibrated a peripheral track system to obtain measurements at 1 degree and 2 degrees from the central fixation. Our study results show that MPOD, L-OD, and Z-OD can be measured at various foveal and parafoveal regions using this protocol at optical infinity. The protocol could be adapted for shorter distances when lengthy rooms are not available in a clinic. In that case, however, pupillary dilation will be necessary to control active accommodation (see Table 1).
There are two critical steps when performing this experiment: 1) the 0 degree calibration and 2) the black calibration. When using the peripheral track system to measure MPOD and its constituents off-center, the external fixation for the 0 degree calibration or foveal measurement is of utmost importance. If the participant whose eye is measured does not understand this procedure or cannot perform the necessary steps, the measurements will be compromised and erroneous. The black calibration is also critical because it allows the MPR to establish a baseline spectrometer measurement when no light is present, which the device then compares to all values obtained from the subject. Therefore, the black calibration is a must for every participant.
Our study results indicate that the central MPOD levels match data from previous published experimental and histological studies7,10,14. Furthermore, we found that the levels for MPOD decline with increasing retinal eccentricity, with MPOD values being greater at the foveal compared to the parafoveal region. The lutein and zeaxanthin levels also vary at different retinal locations with the lutein and zeaxanthin ratios changing as a function of eccentricity. We found central L-OD and Z-OD ratios of 1:2.6, which changed to 2.08:1 at 2 degrees from central fixation. This is consistent with reports from previous studies10,29. We found that the lutein and zeaxanthin levels showed considerable interindividual variation. Prior in vivo laboratory experiments have evaluated only three subjects and there is limited information in this area29. If the significant interindividual variation of levels of carotenoids is correct, then this would support the need to obtain baseline measures of carotenoids and tailoring individual supplements. Further research will be needed to confirm this finding of high interindividual variability of lutein and zeaxanthin levels in healthy individuals. Prior publications and work with this MPR device show that repeatable measurements can be obtained for MPOD in both undilated and dilated pupillary conditions, although the repeatability of L-OD and Z-OD measurements was improved when pupils were dilated25. In the present study, we performed all MPR measurements with dilated pupils. Given that the carotenoid levels are lower at the foveal periphery and parafoveal region, it may be essential to dilate the pupil for consistent signal strength and reliable peripheral measurements.
We tried various methods, and ultimately developed and tested our track system. It proved to be the most effective way to achieve reliable results. The system was tested by examining three participants multiple times to see if similar outcomes could be achieved with each attempt. This included measuring the participants on three separate occasions over a two-month period. Other methods attempted included modifying the reflectometry eyepiece by creating a cover with precut slits at 0, 1, and 2 degrees off center. This technique proved ineffective because the slits were too close together for a subject to adequately distinguish.
There are several limitations in this study. The study requires that the subjects have normal binocularity. This ensures that the subject will be able to fixate on the target while the other eye is being measured. Subjects who do not meet this criterion will be unable to comply with the instructions, will not fixate properly while engaging the stimulus, and cannot be measured successfully using this technique. The track system was reliable, but its limitations could be addressed in future studies. The protocol could be improved by having built-in red LED fixation lights with part of a Badal optometer system as a part of the reflectometer. This would allow the participant to fixate at the desired eccentricity with the eye being measured with appropriate accommodation of lens.
At the present time, there are no alternative techniques to measure in vivo L-OD and Z-OD. However, alternative devices that measure MPOD exist. One such device is the heterochromatic flicker photometer used in this study. The heterochromatic flicker photometer employs a psychophysical method of testing and cannot determine individual lutein and zeaxanthin values. The central MPOD measurements obtained using a heterochromatic flicker photometer were an average of 0.11 lower than those obtained by the MPR device with a standard deviation of 0.16. The MPOD measurement obtained using both the techniques had excellent correlation as reported previously25.
Although the current study has a small sample size, its purpose was to prove the concept that peripheral measurements of zeaxanthin and lutein optical density can be obtained using a reflectometry device. To our knowledge, other in vivo studies have had significantly smaller sample sizes than the sample utilized in this study. Therefore, we are confident that our results demonstrate that in vivo carotenoid density can be measured at the foveola, foveal periphery, and parafoveal region using a reflectometer. Our study sheds further light on how zeaxanthin and lutein levels are distributed in the central and peripheral macular regions within the human retina. Because we found a remarkable variation of the values among our study participants, larger studies both in vivo and in vitro are needed to better understand lutein and zeaxanthin distribution, levels, and ratios within the general population.

Age related macular degeneration (AMD) is a leading cause of blindness and accounts for 8.7% of blindness worldwide1. Risk factors associated with AMD include increasing age, female gender, smoking, light iris color, lipid imbalance, lifetime exposure to sunlight and ultraviolet radiations, systemically lower levels of antioxidants, lower macular pigment optical density (MPOD), genetics, and race2. Of these, modifiable risk factors are smoking cessation, oral supplementation of antioxidants, and carotenoids. Carotenoids are natural pigments found in plants and microorganisms, and are efficient antioxidants3. They are produced by photosynthetic organisms; humans obtain carotenoids from their diet3,4. Macular pigments are composed of three carotenoids: lutein, zeaxanthin, and meso-zeaxanthin4. The xanthophylls lutein and zeaxanthin5 are found in the retina, specifically the macula, and give the fovea its yellow color6. Higher concentrations of xanthophylls are observed in the axons of the photoreceptors and inner plexiform layers of the retina5,7. The intake of carotenoids, like lutein and zeaxanthin, increases the level of macular pigment. Lutein and zeaxanthin are obtained from dietary intake or with nutrient supplementation, while meso-zeaxanthin is simply a byproduct of the metabolism of lutein3,7,8. Lutein and zeaxanthin concentrations differ in the various regions of the retina. Centrally, in the fovea, zeaxanthin concentration is greater than that of lutein, with a ratio of 2.3:19,10. The concentration of carotenoids decreases 100-fold per mm in the foveal periphery, where lutein is more prevalent than zeaxanthin, with a ratio of 2.4:19,10.
The presence of xanthophylls in the retina protects the retinal circuitry, especially in the fovea and macula, and is critical for central vision. The xanthophylls protect the retina by two possible mechanisms: 1) filtering blue light and 2) decreasing oxidative stress5,11,12,13. Blue light scatters the most in the retina and higher levels of macular pigment centrally absorb the scattered light, thereby improving vision. Additionally, the blue part of the visible spectrum is composed of high energy, short wavelengths that can result in the production of excessive amounts of reactive oxygen species in the retina. Therefore, it is thought that carotenoids reduce the oxidative burden on the macula by acting as antioxidants in the inner retina and photoreceptor retinal pigment epithelial complex by quenching these free radicals5,12,13,14.
Measurement of retinal carotenoids has larger implications in systemic health. A recent trial showed that carotenoid therapy improves retinal function in diabetics without any alterations to blood glucose levels15. The levels of carotenoid density in the retina are also strongly correlated with the levels in the brain16. Carotenoid levels may be crucial in the developmental years17,18, and levels in the brain decline with age19. The MPOD levels are related to neuroprotection and neural efficiency in both children and the elderly20,21. Thus, there is a need to measure MPOD and its characteristics clinically. This will play a role in diagnosis, management, and treatment of various ocular and systemic conditions7,15,16,17,18,19,20,21.
The current commercially available MPOD measuring technologies are heterochromatic flicker photometers (HFP), which are based on psychophysical testing. These measure a 1 degree patch on the fovea, which amounts to a ~0.30 mm diameter circle22. While these types of devices have been shown to be reliable, they are limited by their subjective nature, are time consuming to use, and are unable to distinguish the individual quantities of xanthophylls that form MPOD13,22,23,24. The macular pigment reflectometer (see Table of Materials), also referred to as a reflectometer (see Figure 1), addresses these limitations by objectively measuring the MPOD and its individual components of lutein and zeaxanthin (xanthophylls)25. The reflectometer utilizes a UV/IR filtered and collimated quartz halogen source to send a controlled light beam to the retina (see schematic Figure 2) and the internal filters absorb most of the radiation produced. Therefore, there is little to no risk of radiation exposure for the participant. The various chromophores and structures in the human eye and the corresponding absorption and reflectance patterns are well described in the literature26,27,28. Analysis of the reflected light processed by the internal spectrometer allows for the quantitative isolation and measurement of lutein and zeaxanthin optical densities (L-OD, Z-OD) along with overall MPOD. The third retinal carotenoid meso-zeaxanthin is spectrally indistinguishable from zeaxanthin and thus the Z-OD represents a combination of both carotenoids29. Prior work has shown reflectometry to be reliable when measuring central L-OD, Z-OD, and MPOD25,29.
The purpose of the current study is to create a technique that can be utilized to produce in vivo estimates of zeaxanthin and lutein levels in the foveal and parafoveal retinal regions in humans. Additional aims are to compare the findings to previously published laboratory and histology results14,29. The approach developed and described in this manuscript and its utilization alongside reflectometry to measure the perifoveal MPOD is novel. This technique can be used with any existing reflectometry unit without major modification to measure retinal levels of individual carotenoids, such as L-OD and Z-OD, at various foveal and parafoveal locations.
The study presented in this manuscript includes eight participants ranging from 22&#8211;29 years of age. Our methods include first conducting a routine ophthalmic examination to ensure that the study participants meet the inclusion criteria. After obtaining informed consent, each study participant underwent the following four tests: 1) a commercially available heterochromatic flicker photometer device was utilized to obtain a central MPOD measurement; 2) a reflectometer device was utilized to obtain two central measurements; 3) using the same reflectometer device in conjunction with the peripheral track system, measurements of carotenoid levels at a 1 degree eccentricity, that is a 0.30 mm diameter circle, was centered at 0.30 mm from the central fovea; 4) using the same set-up, carotenoid levels at a 2 degree eccentricity, a 0.30 mm diameter circle placed at the edge of the fovea (a parafoveal region), were also measured.
The MPR measurements were performed after dilating each participant&#39;s pupil with 1% tropicamide ophthalmic drops. It is known that pupillary dilation is not needed to obtain MPOD values using reflectometry, but it may improve the repeatability of L-OD and Z-OD measurements25,29. This is possibly due to the fact that measurements obtained from the retina using the reflectometer had better signal-to-noise ratio when the pupils were dilated. For the accurate and stable peripheral reflectometry measurements, participants used fixation targets that were placed at optical infinity30,31.
We obtained reflectometer measurements for 30 s and discarded the first 10 s of data. This procedure has two advantages: 1) the signal source is bright and allows for the eyes to adapt and adjust to the task; and 2) most importantly, the photoreceptor pigment bleaches during the first 10 s. Therefore, eliminating the first 10 s of measurement allows for a more stable and accurate signal29. We performed all reflectometry tests twice in the present study, after which we averaged the measurements to obtain mean MPOD, L-OD, and Z-OD values and the ratio of Z-OD/ L-OD for each participant.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>1-1/4-in x 36-in Silver Under Door Threshold</td>
			<td>Frost King LLC</td>
			<td>77578013947</td>
			<td>Any adjustable strip that can be mounted on a wall will suffice.</td>
		</tr>
		<tr>
			<td>Black electrical tape</td>
			<td>3M Company</td>
			<td>054007-00053</td>
			<td>Used to adjust fixation light to create a 1cm by 1cm region.</td>
		</tr>
		<tr>
			<td>LED lights with remote control</td>
			<td>Elfeland LLC</td>
			<td>ELFELANDhoasupic1295</td>
			<td>Any small red fixation LED light with remote control that can be mounted to track will suffice.</td>
		</tr>
		<tr>
			<td>Macular Pigment Reflectometer</td>
			<td>Zeavision LLC</td>
			<td>N/A</td>
			<td>Prototype not available for sale.</td>
		</tr>
		<tr>
			<td>Quantifeye Macular Pigment Spectromter 2</td>
			<td>Zeavision LLC</td>
			<td>Catalog Number N/A</td>
			<td>Only model available from Zeavision LLC.</td>
		</tr>
		<tr>
			<td>Ultra Gel Control 4g Super Glue</td>
			<td>Henkel AG &#38; Company</td>
			<td>1405419</td>
			<td>Used to fix LED lights to track, but any strong adhesive will suffice.</td>
		</tr>
		<tr>
			<td>Zeavision Proprietary Reflectometry Software, native to Macular Pigment Reflectometer</td>
			<td>Zeavision LLC</td>
			<td>N/A</td>
			<td>The software and algorithm are proprietary to Zeavision LLC.</td>
		</tr>
	</tbody>
</table>

measurement of carotenoids in perifovea using the macular pigment reflectometer

The macular pigment reflectometer (MPR) objectively measures the overall macular pigment optical density (MPOD) and further provides the lutein optical density (L-OD) and zeaxanthin optical density (Z-OD) in the central 1 degree of the fovea. A modification of the technique was developed to evaluate in vivo carotenoid density eccentric to the fovea. An adjustable track system with red LED lights was placed 6.1 m away from the participant to facilitate ocular fixation. Lights were spaced appropriately to create increments of 1 degree retinal disparity during the reflectometry measurements. All reflectometry measurements were obtained with pupillary dilation. The mean MPR-MPOD value for the central measurement was 0.593 (SD 0.161) with an L-OD to Z-OD ratio of 1:2.61. The MPR-MPOD value at 1 degree was 0.248 and the mean MPR-MPOD value at 2 degrees in the parafoveal region was 0.143. The L-OD to Z-OD ratio at 1 degree and 2 degrees off center was 1.38:1.0 and 2.08:1.0, respectively. The results demonstrate that MPOD measurements obtained using the MPR decrease as a function of retinal eccentricity and that there is a higher concentration of zeaxanthin centrally compared to lutein. The L-OD to Z-OD ratio changes with foveal eccentricity, with twice more lutein than zeaxanthin at 2 degrees off center. Our technique successfully provides a quick in vivo method for the measurement of macular pigment optical density at various foveal eccentricities. The results agree with prior published in vivo and in vitro xanthophyll carotenoid density distribution measurements.

This study included eight participants ranging from 22&#8211;29 years of age. Table 1 describes how to calculate the distance to obtain each degree of eccentricity from the center of the macula. Table 2 provides the demographics of the participants. The study sample includes an equal number of males and females with a wide variety of ethno-racial diversity. Table 3 shows the mean results of MPOD obtained by both the devices and L-OD and Z-OD of all participants involved in the study at various eccentricities. The mean MPOD and standard deviation obtained by the heterochromatic flicker photometer and the reflectometry technique was 0.480 (SD 0.14) and 0.593 (SD 0.161) respectively. There was excellent correlation between the MPOD measurement obtained using the techniques with Person correlation coefficient r = 0.92 (p &#60; 0.001). The Z-OD was larger centrally compared to the L-OD measured in the foveal region. The L-OD to Z-OD ratio centrally was 1:2.61. The Z-OD decreased as a function of eccentricity at the center of the fovea. At 1 degree from the central fovea the concentration of Z-OD measured by reflectometry decreased significantly, with an increase in L-OD. The L-OD to Z-OD ratio at 1 degree from central fixation was 1.38:1.0. In the parafoveal region at 2 degrees from central fixation the lutein became the predominant carotenoid and the L-OD to Z-OD ratio was 2.08:1.0. Tables 4, 5, and 6 show the data obtained from all eight subjects. Examining the tables, it is obvious that there is significant interindividual variability of L-OD, Z-OD, and MPOD values, indicating that the physiological limits of normality can be large.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/60429/60429fig1a.jpg" /> 
Figure 1: Macular pigment reflectometer. Macular Pigment Reflectometer used in this experiment. <a href="https://www.jove.com/files/ftp_upload/60429/60429fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/60429/60429fig2a.jpg" /> 
Figure 2: Macular pigment reflectometer operational schematic. Diagram of the internal operational schematics of the MPR device. <a href="https://www.jove.com/files/ftp_upload/60429/60429fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/60429/60429fig3.jpg" /> 
Figure 3: Peripheral measurement track system. (A) The macular pigment reflectometer with the peripheral track system 6.1 m away. (B) The track system with a researcher pointing at the 0 degree LED light. (C) The whole system as it would appear when the participant is being tested. (D) The track system with the 1 degree LED light on. <a href="https://www.jove.com/files/ftp_upload/60429/60429fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/60429/60429fig4.jpg" /> 
Figure 4: Window showing slide bars used for editing measurements to desired time. The slide bars used to edit the desired time frame. The image shows the first 10 s being removed. <a href="https://www.jove.com/files/ftp_upload/60429/60429fig4alarge.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<table border="1" fo:keep-together.within-page="1">
	<tbody>
		<tr>
			<td>Test distance [m]</td>
			<td>3</td>
			<td>4</td>
			<td>5</td>
			<td>6.1</td>
			<td>7</td>
			<td>8</td>
			<td>9</td>
			<td>10</td>
		</tr>
		<tr>
			<td>Distance between lights [m]</td>
			<td>0.052</td>
			<td>0.07</td>
			<td>0.087</td>
			<td>0.107</td>
			<td>0.122</td>
			<td>0.14</td>
			<td>0.157</td>
			<td>0.175</td>
		</tr>
	</tbody>
</table>
Table 1: Separation between fixation lights at various distances from target. The distance between the lights is the value for x in this equation: 
<img alt="Equation 1" src="/files/ftp_upload/60429/60429eq1.jpg" /> 
where d is the test distance.
<table border="1" fo:keep-together.within-page="1">
	<tbody>
		<tr>
			<td>Subject</td>
			<td>Age</td>
			<td>Gender</td>
			<td>Ethnicity</td>
			<td>Race</td>
		</tr>
		<tr>
			<td>3002</td>
			<td>27</td>
			<td>F</td>
			<td>Hispanic</td>
			<td>Caucasian/More than one race</td>
		</tr>
		<tr>
			<td>3003</td>
			<td>28</td>
			<td>F</td>
			<td>Hispanic</td>
			<td>None</td>
		</tr>
		<tr>
			<td>3004</td>
			<td>26</td>
			<td>F</td>
			<td>Not Hispanic</td>
			<td>African American</td>
		</tr>
		<tr>
			<td>3005</td>
			<td>24</td>
			<td>M</td>
			<td>Hispanic</td>
			<td>Asian/More than one race</td>
		</tr>
		<tr>
			<td>3006</td>
			<td>27</td>
			<td>M</td>
			<td>Not Hispanic</td>
			<td>Asian</td>
		</tr>
		<tr>
			<td>3007</td>
			<td>25</td>
			<td>F</td>
			<td>Not Hispanic</td>
			<td>African American</td>
		</tr>
		<tr>
			<td>3009</td>
			<td>29</td>
			<td>M</td>
			<td>Hispanic</td>
			<td>Caucasian/More than one race</td>
		</tr>
		<tr>
			<td>3010</td>
			<td>22</td>
			<td>M</td>
			<td>Not Hispanic</td>
			<td>Asian</td>
		</tr>
	</tbody>
</table>
Table 2: Demographics of participants of the study. Table shows the age, gender, and ethnicity of the tested participants. The average age of the participants was 26. There was a 1:1 ratio of men to women. The self-identified ethnicity of the participants included 50% Hispanic and about 37.5% of either Asian or More Than One Race.
<table border="1" fo:keep-together.within-page="1">
	<tbody>
		<tr>
			<td></td>
			<td>Mean L-OD</td>
			<td>Mean Z-OD</td>
			<td>Mean-reflectometry MPOD</td>
			<td>Mean Z-L Ratio</td>
			<td>Mean-Flicker photomettry MPOD</td>
		</tr>
		<tr>
			<td>Central</td>
			<td>0.247</td>
			<td>0.425</td>
			<td>0.593</td>
			<td>2.61:1</td>
			<td>0.48</td>
		</tr>
		<tr>
			<td>Peripheral 1 deg</td>
			<td>0.402</td>
			<td>0.122</td>
			<td>0.248</td>
			<td>1:1.38</td>
			<td>Not available</td>
		</tr>
		<tr>
			<td>Peripheral 2 deg</td>
			<td>0.366</td>
			<td>0.03</td>
			<td>0.143</td>
			<td>1:2.08</td>
			<td>Not available</td>
		</tr>
	</tbody>
</table>
Table 3: Mean values of carotenoids at various eccentricities. The table shows the mean results from the eight participants in the study. SD for mean central L-OD (0.188) and mean central Z-OD (0.142). SD for Mean Central MPOD of MPR (0.161) and SD for Mean Central MPOD of the reflectometer (0.14). SD for mean L-OD at peripheral 1 degree (0.224) and mean Z-OD at peripheral 1 degree (0.122). SD for mean MPOD of MPR at peripheral 1 degree (0.248). SD for mean L-OD at peripheral 2 degree (0.366) and SD for mean Z-OD at peripheral 2 degree (0.030). SD for mean MPOD of MPR at peripheral 2 degree (0.143).
<table border="1" fo:keep-together.within-page="1">
	<tbody>
		<tr>
			<td>Participant</td>
			<td>L-OD</td>
			<td>Z-OD</td>
			<td>MPOD</td>
			<td>Z-L Ratio</td>
			<td>MPS</td>
		</tr>
		<tr>
			<td>3002</td>
			<td>0.525</td>
			<td>0.409</td>
			<td>0.669</td>
			<td>0.778</td>
			<td>0.58</td>
		</tr>
		<tr>
			<td>3003</td>
			<td>0.566</td>
			<td>0.415</td>
			<td>0.6525</td>
			<td>0.733</td>
			<td>0.48</td>
		</tr>
		<tr>
			<td>3004</td>
			<td>0.1615</td>
			<td>0.291</td>
			<td>0.437</td>
			<td>1.793</td>
			<td>0.437</td>
		</tr>
		<tr>
			<td>3005</td>
			<td>0.121</td>
			<td>0.414</td>
			<td>0.555</td>
			<td>3.432</td>
			<td>0.555</td>
		</tr>
		<tr>
			<td>3006</td>
			<td>0.148</td>
			<td>0.724</td>
			<td>0.888</td>
			<td>4.892</td>
			<td>0.888</td>
		</tr>
		<tr>
			<td>3007</td>
			<td>0.074</td>
			<td>0.389</td>
			<td>0.536</td>
			<td>5.257</td>
			<td>0.536</td>
		</tr>
		<tr>
			<td>3009</td>
			<td>0.197</td>
			<td>0.26</td>
			<td>0.361</td>
			<td>1.32</td>
			<td>0.361</td>
		</tr>
		<tr>
			<td>3010</td>
			<td>0.183</td>
			<td>0.496</td>
			<td>0.642</td>
			<td>2.71</td>
			<td>0.642</td>
		</tr>
	</tbody>
</table>
Table 4: Individual carotenoid optical density measurements obtained at central fixation. Table shows the measurements obtained at central fixation for all eight participants.
<table border="1" fo:keep-together.within-page="1">
	<tbody>
		<tr>
			<td>Participant</td>
			<td>L-OD</td>
			<td>Z-OD</td>
			<td>MPOD</td>
			<td>Z-L Ratio</td>
		</tr>
		<tr>
			<td>3002</td>
			<td>0.325</td>
			<td>0</td>
			<td>0.012</td>
			<td>0</td>
		</tr>
		<tr>
			<td>3003</td>
			<td>0.385</td>
			<td>0.08</td>
			<td>0.166</td>
			<td>0.208</td>
		</tr>
		<tr>
			<td>3004</td>
			<td>0.121</td>
			<td>0.253</td>
			<td>0.392</td>
			<td>2.091</td>
		</tr>
		<tr>
			<td>3005</td>
			<td>0.7015</td>
			<td>0</td>
			<td>0.119</td>
			<td>0</td>
		</tr>
		<tr>
			<td>3006</td>
			<td>0.362</td>
			<td>0.286</td>
			<td>0.45</td>
			<td>0.79</td>
		</tr>
		<tr>
			<td>3007</td>
			<td>0.104</td>
			<td>0.265</td>
			<td>0.391</td>
			<td>2.548</td>
		</tr>
		<tr>
			<td>3009</td>
			<td>0.589</td>
			<td>0</td>
			<td>0.183</td>
			<td>0</td>
		</tr>
		<tr>
			<td>3010</td>
			<td>0.626</td>
			<td>0.094</td>
			<td>0.273</td>
			<td>0.15</td>
		</tr>
	</tbody>
</table>
Table 5: Individual carotenoid optical density measurements obtained at 1 degree from central fixation. Table shows the measurements obtained at 1 degree from central fixation for all eight participants.
<table border="1" fo:keep-together.within-page="1">
	<tbody>
		<tr>
			<td>Participant</td>
			<td>L-OD</td>
			<td>Z-OD</td>
			<td>MPOD</td>
			<td>Z-L Ratio</td>
		</tr>
		<tr>
			<td>3002</td>
			<td>0.146</td>
			<td>0</td>
			<td>0.043</td>
			<td>0</td>
		</tr>
		<tr>
			<td>3003</td>
			<td>0.351</td>
			<td>0</td>
			<td>0.066</td>
			<td>0</td>
		</tr>
		<tr>
			<td>3004</td>
			<td>0.063</td>
			<td>0.077</td>
			<td>0.169</td>
			<td>1.222</td>
		</tr>
		<tr>
			<td>3005</td>
			<td>0.189</td>
			<td>0.017</td>
			<td>0.067</td>
			<td>0.09</td>
		</tr>
		<tr>
			<td>3006</td>
			<td>0.902</td>
			<td>0</td>
			<td>0.291</td>
			<td>0</td>
		</tr>
		<tr>
			<td>3007</td>
			<td>0.04</td>
			<td>0.099</td>
			<td>0.201</td>
			<td>2.475</td>
		</tr>
		<tr>
			<td>3009</td>
			<td>0.718</td>
			<td>0.046</td>
			<td>0.232</td>
			<td>0.064</td>
		</tr>
		<tr>
			<td>3010</td>
			<td>0.518</td>
			<td>0</td>
			<td>0.076</td>
			<td>0</td>
		</tr>
	</tbody>
</table>
Table 6: Individual carotenoid optical density measurements obtained at 2 degrees from central fixation. Table shows the measurements obtained at 2 degrees from central fixation for all eight participants.

Watch this Scientific Journal Video about Measurement of Carotenoids in Perifovea using the Macular Pigment Reflectometer at JoVE.com

Measurement of Carotenoids in Perifovea using the Macular Pigment Reflectometer

We present a protocol to determine the levels of overall macular pigment, lutein, and zeaxanthin optical density in the central and parafoveal regions of the retina. The protocol includes a novel adjustable track system used to measure macular pigment optical density in the foveal eccentricity.

The macular pigment reflectometer (MPR) objectively measures the overall macular pigment optical density (MPOD) and further provides the lutein optical ...

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Medicine

7.1K Views.  Western University of Health Sciences. We present a protocol to determine the levels of overall macular pigment, lutein, and zeaxanthin optical density in the central and parafoveal regions of the retina. The protocol includes a novel adjustable track system used to measure macular pigment optical density in the foveal eccentricity.

Video: Measurement of Carotenoids in Perifovea using the Macular Pigment Reflectometer

Epidural Intracranial Pressure Measurement in Rats Using a Fiber-optic Pressure Transducer

Elevated intracranial pressure (ICP) is a significant problem in several forms of ischemic brain injury including stroke, traumatic brain injury and cardiac arrest. This elevation may result in further neurological injury, in the form of transtentorial herniation1,2,3,4, midbrain compression, neurological deficit or increased cerebral infarct2,4. Current therapies are often inadequate to control elevated ICP in the clinical setting5,6,7 . Thus there is a need for accurate methods of ICP measurement in animal models to further our understanding of the basic mechanisms and to develop new treatments for elevated ICP.
In both the clinical and experimental setting ICP cannot be estimated without direct measurement. Several methods of ICP catheter insertion currently exist. Of these the intraventricular catheter has become the clinical 'gold standard' of ICP measurement in humans8. This method involves the partial removal of skull and the instrumentation of the catheter through brain tissue. Consequently, intraventricular catheters have an infection rate of 6-11%9. For this reason, subdural and epidural cannulations have become the preferred methods in animal models of ischemic injury. 
Various ICP measurement techniques have been adapted for animal models, and of these, fluid-filled telemetry catheters10 and solid state catheters are the most frequently used11,12,13,14,15. The fluid-filled systems are prone to developing air bubbles in the line, resulting in false ICP readings. Solid state probes avoid this problem (Figure 1). An additional problem is fitting catheters under the skull or into the ventricles without causing any brain injury that might alter the experimental outcomes. Therefore, we have developed a method that places an ICP catheter contiguous with the epidural space, but avoids the need to insert it between skull and brain. 
An optic fibre pressure catheter (420LP, SAMBA Sensors, Sweden) was used to measure ICP at the epidural location because the location of the pressure sensor (at the very tip of the catheter) was found to produce a high fidelity ICP signal in this model. There are other manufacturers of similar optic fibre technologies13 that may be used with our methodology. Alternative solid state catheters, which have the pressure sensor located at the side of the catheter tip, would not be appropriate for this model as the signal would be dampened by the presence of the monitoring screw. 
Here, we present a relatively simple and accurate method to measure ICP. This method can be used across a wide range of ICP related animal models.

A novel technique to record the pressures within the skull is described. The minimally invasive method uses a fibre-optic pressure sensing system to accurately measure intracranial pressure (ICP) in anaesthetized rats without causing significant brain trauma. The technique may be used in a wide range of experimental models.

Elevated intracranial pressure (ICP) is a significant problem in several forms of ischemic brain injury including stroke, traumatic brain injury and ...

The Measurement and Treatment of Suppression in Amblyopia

Amblyopia, a developmental disorder of the visual cortex, is one of the leading causes of visual dysfunction in the working age population. Current estimates put the prevalence of amblyopia at approximately 1-3%1-3, the majority of cases being monocular2. Amblyopia is most frequently caused by ocular misalignment (strabismus), blur induced by unequal refractive error (anisometropia), and in some cases by form deprivation.
Although amblyopia is initially caused by abnormal visual input in infancy, once established, the visual deficit often remains when normal visual input has been restored using surgery and/or refractive correction. This is because amblyopia is the result of abnormal visual cortex development rather than a problem with the amblyopic eye itself4,5 . Amblyopia is characterized by both monocular and binocular deficits6,7 which include impaired visual acuity and poor or absent stereopsis respectively. The visual dysfunction in amblyopia is often associated with a strong suppression of the inputs from the amblyopic eye under binocular viewing conditions8. Recent work has indicated that suppression may play a central role in both the monocular and binocular deficits associated with amblyopia9,10 .
Current clinical tests for suppression tend to verify the presence or absence of suppression rather than giving a quantitative measurement of the degree of suppression. Here we describe a technique for measuring amblyopic suppression with a compact, portable device11,12 . The device consists of a laptop computer connected to a pair of virtual reality goggles. The novelty of the technique lies in the way we present visual stimuli to measure suppression. Stimuli are shown to the amblyopic eye at high contrast while the contrast of the stimuli shown to the non-amblyopic eye are varied. Patients perform a simple signal/noise task that allows for a precise measurement of the strength of excitatory binocular interactions. The contrast offset at which neither eye has a performance advantage is a measure of the "balance point" and is a direct measure of suppression. This technique has been validated psychophysically both in control13,14 and patient6,9,11 populations.
In addition to measuring suppression this technique also forms the basis of a novel form of treatment to decrease suppression over time and improve binocular and often monocular function in adult patients with amblyopia12,15,16 . This new treatment approach can be deployed either on the goggle system described above or on a specially modified iPod touch device15.

Amblyopia is a developmental disorder of the visual cortex that is often accompanied by strong suppression of one eye. We present a new technique for measuring and treating interocular suppression in patients with amblyopia that can be deployed using virtual reality goggles or a portable iPod Touch device.

Amblyopia, a developmental disorder of the visual cortex, is one of the leading causes of visual dysfunction in the working age population. Current ...

Detecting Abnormalities in Choroidal Vasculature in a Mouse Model of Age-related Macular Degeneration by Time-course Indocyanine Green Angiography

Indocyanine Green&#160;Angiography (or ICGA) is a technique performed by ophthalmologists to diagnose abnormalities of the choroidal and retinal vasculature of various eye diseases such as age-related macular degeneration (AMD). ICGA is especially useful to image the posterior choroidal vasculature of the eye due to its capability of penetrating through the pigmented layer with its infrared spectrum. ICGA time course can be divided into early, middle, and late phases. The three phases provide valuable information on the pathology of eye problems. Although time-course ICGA by intravenous (IV) injection is widely used in the clinic for the diagnosis and management of choroid problems, ICGA by intraperitoneal injection (IP) is commonly used in animal research. Here we demonstrated the technique to obtain high-resolution ICGA time-course images in mice by tail-vein injection and confocal scanning laser ophthalmoscopy. We used this technique to image the choroidal lesions in a mouse model of age-related macular degeneration. Although it is much easier to introduce ICG to the mouse vasculature by IP, our data indicate that it is difficult to obtain reproducible ICGA time course images by IP-ICGA. In contrast, ICGA via tail vein injection provides high quality ICGA time-course images comparable to human studies. In addition, we showed that ICGA performed on albino mice gives clearer pictures of choroidal vessels than that performed on pigmented mice. We suggest that time-course IV-ICGA should become a standard practice in AMD research based on animal models.

Indocyanine Green Angiography (or ICGA) performed by tail vein injection provides high quality ICGA time course images to characterize abnormalities in mouse choroid.

Indocyanine Green&#160;Angiography (or ICGA) is a technique performed by ophthalmologists to diagnose abnormalities of the choroidal and retinal ...

Performing Subretinal Injections in Rodents to Deliver Retinal Pigment Epithelium Cells in Suspension

The conversion of light into electrical impulses occurs in the outer retina and is accomplished largely by rod and cone photoreceptors and retinal pigment epithelium (RPE) cells. RPE provide critical support for photoreceptors and death or dysfunction of RPE cells is characteristic of age-related macular degeneration (AMD), the leading cause of permanent vision loss in people age 55 and older. While no cure for AMD has been identified, implantation of healthy RPE in diseased eyes may prove to be an effective treatment, and large numbers of RPE cells can be readily generated from pluripotent stem cells. Several interesting questions regarding the safety and efficacy of RPE cell delivery can still be examined in animal models, and well-accepted protocols used to inject RPE have been developed. The technique described here has been used by multiple groups in various studies and involves first creating a hole in the eye with a sharp needle. Then a syringe with a blunt needle loaded with cells is inserted through the hole and passed through the vitreous until it gently touches the RPE. Using this injection method, which is relatively simple and requires minimal equipment, we achieve consistent and efficient integration of stem cell-derived RPE cells in between the host RPE that prevents significant amount of photoreceptor degeneration in animal models. While not part of the actual protocol, we also describe how to determine the extent of the trauma induced by the injection, and how to verify that the cells were injected into the subretinal space using in vivo imaging modalities. Finally, the use of this protocol is not limited to RPE cells; it may be used to inject any compound or cell into the subretinal space.

Here we present a community accepted protocol in multimedia format for subretinally injecting a bolus of RPE cells in rats and mice. This approach can be used for determining rescue potentials, safety profiles, and survival capacities of grafted RPE cells upon implantation in animal models of retinal degeneration.

The conversion of light into electrical impulses occurs in the outer retina and is accomplished largely by rod and cone photoreceptors and retinal pigment ...

Measurement of the Pressure-volume Curve in Mouse Lungs

In recent decades the mouse has become the primary animal model of a variety of lung diseases. In models of emphysema or fibrosis, the essential phenotypic changes are best assessed by measurement of the changes in lung elasticity. To best understand specific mechanisms underlying such pathologies in mice, it is essential to make functional measurements that can reflect the developing pathology. Although there are many ways to measure elasticity, the classical method is that of the total lung pressure-volume (PV) curve done over the whole range of lung volumes. This measurement has been made on adult lungs from nearly all mammalian species dating back almost 100 years, and such PV curves also played a major role in the discovery and understanding of the function of pulmonary surfactant in fetal lung development. Unfortunately, such total PV curves have not been widely reported in the mouse, despite the fact that they can provide useful information on the macroscopic effects of structural changes in the lung. Although partial PV curves measuring just the changes in lung volume are sometimes reported, without a measure of absolute volume, the nonlinear nature of the total PV curve makes these partial ones very difficult to interpret. In the present study, we describe a standardized way to measure the total PV curve. We have then tested the ability of these curves to detect changes in mouse lung structure in two common lung pathologies, emphysema and fibrosis. Results showed significant changes in several variables consistent with expected structural changes with these pathologies. This measurement of the lung PV curve in mice thus provides a straightforward means to monitor the progression of the pathophysiologic changes over time and the potential effect of therapeutic procedures.

Here we present a protocol to simply and reliably measure the lung pressure-volume curve in mice, showing that it is sufficiently sensitive to detect phenotypic parenchymal changes in two common lung pathologies, pulmonary fibrosis and emphysema. This metric provides a means to quantify the lung&#8217;s structural changes with developing pathology.

In recent decades the mouse has become the primary animal model of a variety of lung diseases. In models of emphysema or fibrosis, the essential ...

Long-term Blood Pressure Measurement in Freely Moving Mice Using Telemetry

During the development of new vasoactive agents, arterial blood pressure monitoring is crucial for evaluating the efficacy of the new proposed drugs. Indeed, research focusing on the discovery of new potential therapeutic targets using genetically altered mice requires a reliable, long-term assessment of the systemic arterial pressure variation. Currently, the gold standard for obtaining long-term measurements of blood pressure in ambulatory mice uses implantable radio-transmitters, which require&#160;artery cannulation. This technique eliminates the need for tethering, restraining, or anesthetizing the animals which introduce stress and artifacts during data sampling. However, arterial blood pressure monitoring in mice via catheterization can be rather challenging due to the small size of the arteries. Here we present a step-by-step guide to illustrate the crucial key passages for a successful subcutaneous implantation of radio-transmitters and carotid artery cannulation in mice. We also include examples of long-term blood pressure activity taken from freely moving mice after a period of post-surgery recovery. Following this procedure will allow reliable direct blood pressure recordings from multiple animals simultaneously.

The goal of this protocol is to assess systemic blood pressure in conscious freely moving mice using implantable radio-telemetry devices.

During the development of new vasoactive agents, arterial blood pressure monitoring is crucial for evaluating the efficacy of the new proposed drugs. ...

Absolute Quantification of A&#946;1-42 in CSF Using a Mass Spectrometric Reference Measurement Procedure

Alzheimer's disease (AD) is the most common neurodegenerative disease among the elderly and accounts for 60-80% of all cases of dementia. Currently, the diagnosis of AD is based on cognitive tests and mental state exams, but the peptide amyloid-beta (A&#946;) in cerebrospinal fluid (CSF) is increasingly used in clinical trials and settings. As for most protein and peptide biomarkers, quantification is performed using antibody-based techniques, such as enzyme-linked immunosorbent assay (ELISA). However, intra- and inter-laboratory variability in these assays hamper its use as a diagnostic marker in clinical routine.
An antibody-independent Reference Measurement Procedure (RMP) was developed based on solid-phase extraction (SPE) and liquid chromatography (LC)-tandem mass spectrometry (MS/MS), where stable, isotope-labeled A&#946; peptides were used as internal standards, enabling absolute quantification. A high-resolution quadrupole-orbitrap hybrid instrument was used for the measurements. The method allows for the quantification of CSF A&#946;1-42 between 150-4,000 pg/mL.

Absolute Quantification of A&amp;#946;&lt;sub&gt;1-42&lt;/sub&gt; in CSF Using a Mass Spectrometric Reference Measurement Procedure

A reference measurement procedure for the absolute quantification of A&#946;1-42 in human CSF based on solid-phase extraction and liquid chromatography tandem mass spectrometry is described.

Alzheimer's disease (AD) is the most common neurodegenerative disease among the elderly and accounts for 60-80% of all cases of dementia. Currently, the ...

Preparation Steps for Measurement of Reactivity in Mouse Retinal Arterioles Ex Vivo

Vascular insufficiency and alterations in normal retinal perfusion are among the major factors for the pathogenesis of various sight-threatening ocular diseases, such as diabetic retinopathy, hypertensive retinopathy, and possibly glaucoma. Therefore, retinal microvascular preparations are pivotal tools for physiological and pharmacological studies to delineate the underlying pathophysiological mechanisms and to design therapies for the diseases. Despite the wide use of mouse models in ophthalmic research, studies on retinal vascular reactivity are scarce in this species. A major reason for this discrepancy is the challenging isolation procedures owing to the small size of these retinal blood vessels, which is ~ &#8804; 30 &#181;m in luminal diameter. To circumvent the problem of direct isolation of these retinal microvessels for functional studies, we established an isolation and preparation technique that enables ex vivo studies of mouse retinal vasoactivity under near-physiological conditions. Although the present experimental preparations will specifically refer to the mouse retinal arterioles, this methodology can readily be employed to microvessels from rats.

Preparation Steps for Measurement of Reactivity in Mouse Retinal Arterioles Ex Vivo

Many vision-threatening ocular diseases are associated with dysfunctional retinal microvessels. Therefore, the measurement of retinal arteriole responses is important to investigate the underlying pathophysiological mechanisms. This article describes a detailed protocol for mouse retinal arteriole isolation and preparation to assess the effects of vasoactive substances on vascular diameter.

Vascular insufficiency and alterations in normal retinal perfusion are among the major factors for the pathogenesis of various sight-threatening ocular ...

Regenerative Therapy by Suprachoroidal Cell Autograft in Dry Age-related Macular Degeneration: Preliminary In Vivo Report

This study is aimed at examining whether a suprachoroidal graft of autologous cells can improve best corrected visual acuity (BCVA) and responses to microperimetry (MY) in eyes affected by dry Age-related Macular Degeneration (AMD) over time through the production and secretion of growth factors (GFs) on surrounding tissue. Patients were randomly assigned to each study group. All patients were diagnosed with dry AMD and with BCVA equal to or greater than 1 logarithm of the minimum angle of resolution (logMAR). A suprachoroidal autologous graft by Limoli Retinal Restoration Technique (LRRT) was carried out on group A, which included 11 eyes from 11 patients. The technique was performed by implanting adipocytes, adipose-derived stem cells obtained from the stromal vascular fraction, and platelets from platelet-rich plasma in the suprachoroidal space. Conversely, group B, including 14 eyes of 14 patients, was used as a control group. For each patient, diagnosis was verified by confocal scanning laser ophthalmoscope and spectral domain-optical coherence tomography (SD-OCT). In group A, BCVA improved by 0.581 to 0.504 at 90 days and to 0.376 logMAR at 180 days (+32.20%) postoperatively. Furthermore, MY test increased by 11.44 dB to 12.59 dB at 180 days. The different cell types grafted behind the choroid were able to ensure constant GF secretion in the choroidal flow. Consequently, the results indicate that visual acuity (VA) in the grafted group can increase more than in the control group after six months.

Regenerative Therapy by Suprachoroidal Cell Autograft in Dry Age-related Macular Degeneration: Preliminary In Vivo Report

The goal of this study is to assess whether the suprachoroidal graft of adipose-derived stem cells included in the stromal vascular fraction and platelets derived from platelet-rich plasma by the Limoli Retinal Restoration Technique can improve visual acuity and retinal sensitivity responses in eyes affected by dry age-related macular degeneration.

This study is aimed at examining whether a suprachoroidal graft of autologous cells can improve best corrected visual acuity (BCVA) and responses to ...

Isometric Contractility Measurement of the Mouse Mesenteric Artery Using Wire Myography

The wire myograph technique is used to assess the contractility of vascular smooth muscles in response to depolarization, GPCR agonists/inhibitors and drugs. It is widely used in many studies on the physiological functions of vascular smooth muscle, the pathogenesis of vascular diseases such as hypertension, and the development of smooth muscle relaxant drugs. The mouse is a widely used model animal with a large pool of disease models and genetically modified strains. We introduced this method to measure the isometric contraction of mouse mesenteric artery in detail. A 1.4-mm segment of mouse mesenteric resistance artery was isolated and mounted on a myograph chamber by passing two steel wires through its lumen. After equilibration and normalization steps, the vessel segment was potentiated by a high-K+ solution twice prior to the contraction assay. As an example of the application of this method in drug development, we measured the relaxant effect of a novel natural substance, neoliensinine, isolated from a Chinese herb, embryos of the lotus seed (Nelumbo nucifera Gaertn.) on mouse mesenteric arteries. The vessel segments mounted on the myograph chamber were stimulated with a high-K+ solution. When the force tension reached a stable sustained phase, cumulative doses of neoliensinine were added to the chamber. We found that neoliensinine had a dose-dependent relaxant effect on smooth muscle contraction, thus suggesting that it bears potential activity against hypertension. In addition, as the vessel segment can survive at least 4 hours after mounting and maintain contractility induced by the high-K+ solution for many times, we suggest that the wire myograph system may be used for the time-consuming process of drug screening.

The wire myograph technique is used to investigate vascular smooth muscle functions and screen new drugs. We report a detailed protocol for measuring the isometric contractility of the mouse mesenteric artery and for screening new relaxants of vascular smooth muscle.

The wire myograph technique is used to assess the contractility of vascular smooth muscles in response to depolarization, GPCR agonists/inhibitors and ...