The authors wish to acknowledge the following: Dr. Joseph Bronzino, Dr. Khamis Abu-Hassaballah, Mr. R.J. Austin-LaFrance, and Ms. Jessica Koranda.

This protocol is appropriate for mice of 3 and 18 months of age and approximate body weight of 30-50 g). Mice can be obtained from The Jackson Laboratory (Bar Harbor, ME). All surgical and experimental protocols were approved by the Trinity College Animal Care and Use Committee and were in accordance with the NIH Guide for the Care and Use of Laboratory Animals.
1. Animal Preparation and Surgical Procedures
<ol>
	<li>Prepare anesthesia cocktail containing ketamine (25 mg/ml), xylazine (2.5 mg/ml) and acepromazine (0.5 mg/ml). Inject 1 ml/kg body weight in the lower right quadrant of the abdomen supplemented by 0.2 ml/kg injections every 45 min&#160;thereafter to maintain a stable depth of anesthesia using the pedal withdrawal reflex.</li>
	<li>Prepare anesthetized mouse for surgery by shaving the fur on its cranium using an electric shaver. The shaved area should include the middle of the eyes to the middle of the ears. Make sure not to shave the whiskers as they are part of the mouse barrel sensory system.</li>
	<li>Use cotton swabs to apply isopropyl alcohol followed by Betadine to the shaved area on the head. Then, also using cotton swabs, apply a small amount of mineral oil on the eyes to prevent the eyeballs from drying.</li>
	<li>Use infant rat ear cuffs instead of regular ear bars to mount the animal&#8217;s head on the stereotaxic frame apparatus. To do this, first mount the left ear on the left ear cuff. Then gently ease the right ear onto the right cuff by gently supporting the animal&#8217;s head with one hand and advancing the ear cuff with the other hand. Next, place a heating pad under the animal&#8217;s body and set it to 86 &#176;F to maintain body temperature.</li>
	<li>Then, check for bilateral rigidity by attempting to move the head side to side. The animal is properly mounted on the stereotaxic frame when the head is rigid and cannot be moved side to side but can easily pivot up and down.</li>
	<li>Gently rest the mouse&#8217;s snout on the nose/tooth bar assembly making sure that the incisors are resting gently but securely within the tooth aperture of the nose/tooth bar.</li>
	<li>Using a sterile scalpel, make a midline incision starting from the middle of the eyes to the middle of the ears. Make sure the scalpel is be held at a 45&#176;&#160;angle and apply enough pressure to cut through the underlying fascia but not through the skull as that will cause excessive bleeding.</li>
	<li>Use cotton swabs to separate the fascia and expose the skull. Skull landmarks bregma and lambda should be clearly visible (Figure&#160;1A). Ensure that the animal is in the skull flat position by adjusting the nose/tooth bar such that bregma and lambda landmarks are at same the dorsoventral (DV) position (+ 0.1 mm).</li>
	<li>Apply a small amount of sterile saline to the exposed area and use cotton swabs to gently clean the skull. Then wait 2-3 min&#160;for the skull to completely air dry before proceeding.</li>
	<li>Mount a needle on the left stereotaxic arm to measure the DV position of bregma and lambda. The DV positioning of these two landmarks should be within 0.1 mm of each other. If not, the nose bar of the stereotaxic frame can be adjusted up and down to achieve this.</li>
	<li>Position the needle on bregma to record its anterior-posterior (AP), lateral (LAT) and dorsoventral (DV) measurements. Be sure the needle just touches the skull and does not penetrate it.</li>
	<li>Use a mouse brain atlas, such as &#8220;The Mouse Brain in Stereotaxic Coordinates&#8221;1, to determine the coordinates for the target structures: medial perforant pathway (mPP) in the angular bundle and dentate gyrus (DG) of the hippocampus, relative to lambda and bregma, respectively (also see Table 1). Then, use a fine-point pen or pencil to mark these points on the skull.</li>
	<li>Also, mark two more points on the contralateral side of the skull. These points which will serve as ground (GND) and reference (REF) should be about 3 mm from the midline and positioned longitudinally relative to each other (Figure&#160;1A, also Table 1).</li>
	<li>Remove the needle marker from the left stereotaxic arm and replace it with an electric dental drill equipped with a stereotaxic mount. Position the drill over each marked point and make small burr holes of approximately 0.5 mm in diameter. When drilling, use a repetitive up-and-down motion and check frequently whether the drill has penetrated the skull to expose the brain surface.</li>
	<li>Gently but firmly drive a screw electrode (#0-80 1/8 in stainless steel machine screws, slotted fillister head) in each of the contralateral holes (GND and REF) such that they just touch the cortical surface without penetrating it (Figure&#160;1A). These two screw electrodes serve as ground and reference.</li>
	<li>Mount stimulating and recording electrodes in electrode holders on the left and right stereotaxic arms, respectively.</li>
	<li>Connect the stimulating electrode terminals to an electrophysiological stimulator with current isolation and the recording electrode terminal to an electrophysiological differential amplifier (gain = 1,000, bandpass filter = 1 Hz&#8211;3 kHz) and then to a digital oscilloscope for visual inspection of evoked responses. &#160;Also, connect GND and REF electrode terminals to the differential amplifier.</li>
	<li>Gently and slowly lower both stimulating and recording electrodes in 0.5 mm increments while visually monitoring the evoked response to a stimulus shock of 600-800 uA. Continue to lower each electrode until they reach their respective target DV position and a stereotypical signal is observed on the oscilloscope (Figure&#160;1B).</li>
	<li>Afterward, use dental acrylic cement to make a cap to hold the electrode terminals in place; any dental cement that touches the skin should be wiped off immediately.&#160; Once the dental cement is completely cured transfer the animal from the stereotaxic frame to a clean rodent cage. Use a heating lamp or pad to maintain core temperature.</li>
	<li>Monitor the animal every hour until it regains consciousness. An injection of flunixin may be administered as an analgesic.</li>
</ol>
2. LTP Induction
<ol>
	<li>Allow the animal 5-7 days to recover from surgery. Place the animal in the recording environment consisting of a faraday cage (122 cm x&#160;43 cm x&#160;43 cm) outfitted with soundproofing material and a 5-channel rotating commutator connecting the electrode leads to the stimulating/recording setup.</li>
	<li>Allow the animal to acclimate for 1-2 hr in the recording environment before connecting the electrodes to the stimulating and recording instruments (refer to step 1.17).</li>
	<li>Set the stimulator controls to output 400 uA and record the amplitude of an average of 10 evoked responses making sure that at least 10 sec&#160;elapse between stimuli. Use the method shown in Figure&#160;1C to quantify the evoked response. Repeat this procedure for 600, 800, 1,000, 1,200, and 1,400 uA.</li>
	<li>Construct an input/output curve by plotting the average amplitude of the evoked response versus stimulus intensity. From this plot determine the stimulus intensity which corresponds to 50% of the maximum amplitude measured. Use the 50% intensity for the remainder of the experiment.</li>
	<li>Then, using the 50% stimulus intensity, obtain a baseline by recording the average amplitude of 5 evoked responses every minute&#160;for 15 min. Again make sure that at least 10 sec&#160;elapse between stimuli.</li>
	<li>Subsequently deliver the tetanic stimulation consisting of 10 bursts of 10 pulses delivered at 400 Hz with a burst rate of 5 Hz to the medial perforant pathway. Monitor the animal closely for signs of seizure, including wet dog shakes. If the animal has a seizure the experiment should be terminated and all data from that animal should be excluded from the study results.</li>
	<li>Then, continue to record the average amplitude of 5 evoked responses every minute for 30 min&#160;posttetanization. After that, compare this amplitude to the baseline amplitude obtained in step 2.5 by calculating the percent change from baseline (Figure&#160;2).</li>
	<li>Following the conclusion of experiments, the animal is euthanized by means of inhalation of isoflurane&#8212;a method which is consistent with the Guidelines on Euthanasia of the American Veterinary Medical Association.</li>
</ol>

<ol>
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Authors have nothing to disclose.

In this protocol, we have demonstrated a reliable and simple method for studying LTP in DG in freely behaving mice. While many studies of LTP in awake rats have been performed3,4, very few have been conducted in awake mice primarily due to the technical complexity posed by the limited cranial real estate in mice and the weight of electrode headstages relative to the average weight of mice5. The few studies that have demonstrated LTP in DG in freely behaving mice utilized either microdrive electrode ...

The development of technology to manipulate genes has produced transgenic and knockout mouse models of almost every neurodegenerative and neurological diseases. This has necessitated translation of electrophysiological research techniques previously used in larger rodent species to the mouse animal model. One such neurophysiological investigation technique is the use long-term potentiation (LTP) to test the efficacy of synaptic connections within neuronal networks involved in various neuropathological disorders. This protocol describes techniques for reliable electrophysiological investigation of LTP in freely behaving mice. The advantage of this protocol over others is that it is simple and easy to implement; it is also rather less costly as it does not require neither the use of expensive computer-controlled microdrive systems nor field effect transistor headstages; and, to our knowledge, is the first video protocol of chronic electrophysiological recordings to study LTP in freely behaving mice. To this end, we describe in this article simple methodologies for studying long-term potentiation in freely behaving mice. These methodologies can readily be translated to transgenic and knockout mouse models of neuropathological disorders.

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	<colgroup>
		<col />
		<col />
		<col />
		<col />
	</colgroup>
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:195px;">Ketamine (100 mg/ml)</td>
			<td style="width:104px;">Henry Schein</td>
			<td style="width:137px;">10177</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:195px;">Xylazine (20 mg/ml)</td>
			<td style="width:104px;">Henry Schein</td>
			<td style="width:137px;">33197</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:195px;">Acepromazine (10 mg/ml)</td>
			<td style="width:104px;">Henry Schein</td>
			<td style="width:137px;">2177</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:195px;">Dental acrylic powder</td>
			<td style="width:104px;">Lang Dental Manufacturing Co.</td>
			<td style="width:137px;">1330CLR</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:195px;">Dental acrylic liquid</td>
			<td style="width:104px;">Lang Dental Manufacturing Co.</td>
			<td style="width:137px;">1306CLR</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:195px;">Tungsten wire (0.127 mm)</td>
			<td style="width:104px;">World Precision Instruments</td>
			<td style="width:137px;">TGW0515</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:195px;">Stainless Steel Hypodermic Tubing (0.286 mm)</td>
			<td style="width:104px;">World Precision Instruments</td>
			<td style="width:137px;">832400</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:195px;">Flunixin (50 mg/ml)</td>
			<td style="width:104px;">Henry Schein</td>
			<td style="width:137px;">14165</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:195px;">Epoxilyte</td>
			<td style="width:104px;">Superior Essex</td>
			<td style="width:137px;">EP 6001-M</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:195px;">Stainless steel wire insert (0.2 mm)</td>
			<td style="width:104px;">World Precision Instruments</td>
			<td>792900</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:195px;">Stereotaxic frame apparatus</td>
			<td style="width:95px;">Kopf Instruments</td>
			<td style="width:137px;">Model 902</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:195px;">Ear cuffs (ear cups)</td>
			<td style="width:95px;">Kopf Instruments</td>
			<td style="width:137px;">Model 921&#160;</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:195px;">Electrophysiological stimulator</td>
			<td style="width:95px;">Astro-Med, Inc.</td>
			<td style="width:137px;">S88</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:195px;">Digital oscilloscope</td>
			<td style="width:95px;">B &#38; K Precision Corp.</td>
			<td style="width:137px;">2542</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:195px;">Current isolation unit</td>
			<td style="width:95px;">Astro-Med, Inc.</td>
			<td style="width:137px;">PSIU-6</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="84">
			<td height="84" style="height:84px;width:195px;">Differential amplifier</td>
			<td style="width:95px;">World Precision Instruments, Inc.</td>
			<td style="width:137px;">DAM-50</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:195px;">Commutator</td>
			<td style="width:95px;">Plastics One</td>
			<td style="width:137px;">SLC6</td>
			<td style="width:79px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:195px;">Dental drill</td>
			<td style="width:95px;">Stoelting</td>
			<td style="width:137px;">58650</td>
			<td style="width:79px;"></td>
		</tr>
	</tbody>
</table>

long-term potentiation of perforant pathway-dentate gyrus synapse in freely behaving mice

Studies of long-term potentiation of synaptic efficacy, an activity-dependent synaptic phenomenon having properties that make it attractive as a potential cellular mechanism underlying learning and information storage, have long been used to elucidate the physiology of various neuronal circuits in the hippocampus, amygdala, and other limbic and cortical structures. With this in mind, transgenic mouse models of neurological diseases represent useful platforms to conduct long-term&#160;potentiation (LTP) studies to develop a greater understanding of the role of genes in normal and abnormal synaptic communication in neuronal networks involved in learning, emotion and information processing. This article describes methodologies for reliably inducing LTP in the freely behaving mouse. These methodologies can be used in studies of transgenic and knockout freely&#160;behaving mouse models of neurodegenerative diseases.

Table 1 shows the coordinates for DG and mPP as used in this protocol. Figure&#160;1A shows the markings for the target structures on the skull; also shown are the location of the ground and reference electrodes. Figure&#160;1B illustrates representative evoked response traces both pre- and posttetanization in the same animal. Note that the posttetanization evoked response is larger than the pretetanization response which is indicative of LTP induction2. <stro...

Watch this Scientific Journal Video about Long-term Potentiation of Perforant Pathway-dentate Gyrus Synapse in Freely Behaving Mice at JoVE.com

Long-term Potentiation of Perforant Pathway-dentate Gyrus Synapse in Freely Behaving Mice

Transgenic and knockout mouse models of neurological diseases are useful for studying the role of genes in normal and abnormal neurophysiology. This article describes methodologies which can be used to study long-term potentiation, a cellular mechanism which may underlie learning and memory, in transgenic and knockout freely&#160;behaving mouse models of neuropathology.

Studies of long-term potentiation of synaptic efficacy, an activity-dependent synaptic phenomenon having properties that make it attractive as a potential ...

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14.0K Views.  Trinity College. Transgenic and knockout mouse models of neurological diseases are useful for studying the role of genes in normal and abnormal neurophysiology. This article describes methodologies which can be used to study long-term potentiation, a cellular mechanism which may underlie learning and memory, in transgenic and knockout freely behaving mouse models of neuropathology.