Muscle Velocity Recovery Cycles to Examine Muscle Membrane Properties

Summary

Presented here is a protocol for the recording of muscle velocity recovery cycles (MVRCs), a new method of examining muscle membrane properties. MVRCs enable in vivo assessment of muscle membrane potential and alterations in muscle ion channel function in relation to pathology, and it enables the demonstration of muscle depolarization in neurogenic muscles.

Abstract

Although conventional nerve conduction studies (NCS) and electromyography (EMG) are suitable for the diagnosis of neuromuscular disorders, they provide limited information about muscle fiber membrane properties and underlying disease mechanisms. Muscle velocity recovery cycles (MVRCs) illustrate how the velocity of a muscle action potential depends on the time after a preceding action potential. MVRCs are closely related to changes in membrane potential that follow an action potential, thereby providing information about muscle fiber membrane properties. MVRCs may be recorded quickly and easily by direct stimulation and recording from multi-fiber bundles in vivo. MVRCs have been helpful in understanding disease mechanisms in several neuromuscular disorders. Studies in patients with channelopathies have demonstrated the different effects of specific ion channel mutations on muscle excitability. MVRCs have been previously tested in patients with neurogenic muscles. In this prior study, muscle relative refraction period (MRRP) was prolonged, and early supernormality (ESN) and late supernormality (LSN) were reduced in patients compared to healthy controls. Thereby, MVRCs can provide in vivo evidence of membrane depolarization in intact human muscle fibers that underlie their reduced excitability. The protocol presented here describes how to record MVRCs and analyze the recordings. MVRCs can serve as a fast, simple, and useful method for revealing disease mechanisms across a broad range of neuromuscular disorders.

Introduction

Nerve conduction studies (NCS) and electromyography (EMG) are the conventional electrophysiological methods used for the diagnosis of neuromuscular disorders. NCS enables detection of axonal loss and demyelination in the nerves¹, while EMG can differentiate whether myopathy or neurogenic changes are present in the muscle due to nerve damage. However, NCS or EMG provide limited information about muscle fiber membrane properties and underlying disease mechanisms. This information can be achieved using intracellular electrodes in isolated muscles from muscle biopsies^2,3,4. However, it is of clinical importance to use methodologies using recordings from intact muscles in patients.

The velocity of a second muscle fiber action potential changes as a function of the delay after the first⁵, and this velocity recovery function (or recovery cycle) has been shown to change in dystrophic or denervated muscles. The yield of such recordings from single muscle fibers was, however, too low to be of use as a clinical tool⁶. However, Z'Graggen and Bostock later found that multi-fiber recordings, obtained by direct stimulation and recording from the same bundle of muscle fibers, provide a fast and simple method of obtaining such recordings in vivo⁷. A sequence of paired pulse electrical stimuli with varying interstimulus intervals (ISIs) is used in this method^7,8,9,10,11.

The evaluated MVRC parameters include the following: 1) muscle relative refractory period (MRRP), which is the duration after a muscle action potential until the next action potential can be elicited; 2) early supernormality (ESN); and 3) late supernormality (LSN). ESN and LSN are the periods after the refractory period in which the action potentials are conducted along the muscle membrane faster than normal. The depolarizing afterpotential, and potassium accumulation in the t-tubules of the muscle respectively, are hypothesized as the main causes for the two periods of supernormality.

The wide applicability of MVRCs to muscle disorders has been shown in detecting membrane depolarization in ischemia^7,10,12 and renal failure¹³, as well as providing information about muscle membrane abnormalities in critical illness myopathy¹⁴ and inclusion body myositis¹⁵. Frequency ramp and intermittent 15 Hz and 20 Hz simulation protocols have since been introduced. MVRCs, together with these additional protocols, have demonstrated the different effects on muscle membrane excitability related to loss-of-function or gain-of-function mutations in various muscle ion channels in the inherited muscle ion channelopathies (i.e., sodium channel myotonia, paramyotonia congenita¹⁶, myotonic dystrophy¹⁷, Andersen-Tawil syndrome¹⁸, and myotonia congenita^19,20).

In a recent study, the applicability of MVRCs to neurogenic muscles was shown for the first time. The term "neurogenic muscle" refers to the secondary changes in skeletal muscles that develop as denervation and reinnervation after any injury to the anterior horn cells or motor axons. Denervation is characterized in EMG as spontaneous activity (i.e., fibrillations [fibs] and positive sharp waves [psws]), while large motor unit potentials with prolonged duration and increased amplitude present reinnervation²¹. EMG changes are evident in denervated muscles, but the underlying cellular changes in muscle fiber membrane potentials have only been demonstrated in experimental studies on isolated muscle tissue^2,3,4. MVRCs provide further insight into in vivo human muscle membrane properties regarding the denervation process.

This paper describes the methodology of MVRCs in detail. It also summarizes the changes in neurogenic muscles in a subgroup of patients from a previously reported study²² and healthy control subjects that enables determination of whether the method is appropriate for a planned study.

The recordings are performing using a recording protocol that is part of a software program. Other equipment used is an isolated linear bipolar constant current stimulator, 50 Hz noise eliminator, isolated electromyography amplifier, and analogue-to-digital converter.

Protocol

All subjects must provide written consent prior to examination, and the protocol must be approved by the appropriate local ethical review board. All methods described here were approved by the Regional Scientific Ethical Committee and Danish Data Protection Agency.

1. Preparation of the subject

1. Assess subjects' medical histories to ensure that they do not have any previous nervous system disorders other than the disease group that will be investigated.
2. Inform the subject in detail about the examinations and request to obtain written consent.
   1. Inform the subject about the insertion of two needles in a leg muscle and that the muscle fibers will be stimulated with weak current.
   2. Explain that the sensation may feel slightly unpleasant.
   3. Inform the subject that the stimulation can be turned off immediately at any moment during the recording in case of any discomfort.
3. Clean the subject's lower leg with alcohol.
4. Insert the stimulating monopolar needle electrode (25 mm x 26 G) over the anterior tibial muscle and adhesive surface electrode as the anode 1 cm distal to the monopolar needle (Figure 1).
5. Place a ground electrode distal to the anode.
6. Insert the recording concentric needle electrode (25 mm x 30 G) about 2cm proximal to the stimulating monopolar needle electrode along the muscle fibers (Figure 1).
7. Connect the recording concentric needle and ground electrodes to the preamplifier.
8. Ask the subject to remain silent and avoid movement during the examination.
9. Zero the output of the stimulator and connect the stimulating electrodes to the stimulator (Figure 1).
10. Maintain the skin temperature between 32–36 °C using a warming lamp.

2. Recording of the MVRCs

1. Start the semi-automated recording software using the muscle excitability recording protocol and turn on the stimulator. Stimulations will start at 2.5 mA with 1 Hz.
2. Increase the stimulus intensity manually by hitting the Insert key until a response is recorded (max = 10 mA).
   1. Adjust the stimulating and recording needles if necessary, until recording an acceptable response with a stimulus intensity of less than 10 mA. The shape of the muscle action potential should be triphasic, if possible, and stable. Avoid large twitches of the whole muscle.
   2. Invert the muscle action potential by hitting the minus key (-) if the potential appears upside down.
      NOTE: A magenta horizontal line appears on the screen indicating the width of the action potential.
3. Adjust the position and length of the magenta line by dragging the line with the mouse. The green horizontal line represents the baseline.
4. Click OK to start recording the MVRCs.
5. Select a stimulus response relationship from the main options.
6. Increase stimulus intensity by hitting the Insert key to a max of 10 mA or tolerable.
7. Click OK to start descending the stimulus response curve.
8. Click OK when the test stimulus reaches zero.
9. Set the stimulus intensity to level for stable latency.
10. Click OK to return to the main menu.
11. Select the option 1/2/5 conditioning stims for RC.
12. Select a protocol from recovery cycle options (e.g., start quick recovery cycle [skip alternate delays]), which is the default.
    NOTE: The recording continues automatically for 34 steps with decreasing inter-stimulus intervals (ISIs).
13. Make sure that muscle action potential is stable during the recording and that the needle has not moved. The screen changes automatically to main options when the 34 steps have completed.
14. Click on Finish recording | Close file | OK, unless a ramp-up frequency or 20 Hz s recordings is being performed.
15. Finish the recording and save the data by clicking on the Close file and save data button.

3. MVRC analyses

1. Start the analyzing software program to perform the analysis offline.
2. Select the recording that will be analysed and click on the OK button.
3. Click on Load parameters from the Files menu.
4. Select MANAL9 option for the analysis. If this is not present on the list, click on Browse to find this file. Click OK to continue.
5. When a description of MAnal9 muscle excitability analysis appears, click OK to continue.
   1. Invert the muscle action potential by typing MM-1 if the potential appears upside down.
   2. Right-click the mouse to make the magenta line visible. Set the window to the base of the peak response and with a width corresponding roughly to the width of the action potential at that height. Drag with the mouse to adjust the window. The window determines the latencies within which the height and latency are measured, as indicated by the pale blue lines, and green line indicates the baseline. Click OK to continue.
6. Click OK to remeasure the latencies and peaks. This will be done automatically.
   NOTE: In the display of the remeasured latencies, the latencies are measured to shorter delays than original ones. This is because the responses to conditioning stimuli alone were subtracted from responses to the conditioning plus the test. This ensures that conditioning stimuli do not interfere with latency measurements. As is indicated in the prompt box, single bad points can be eliminated by positioning the cursor (vertical red line) over the point and hitting the ~ key. The bad point is replaced with mean of values on either side in same channel. If there are no bad points, set DE (display end) to just after the last latency required.
7. Click OK to create an RMC file.
8. Ignore most of the options appearing in the "Create RCC or RMC" form, since these are concerned with measurements of C-fiber rather than MVRCs. Click Save and Exit to continue. After saving the RMC file, the prompt box provides different options
9. If frequency ramp and/or repetitive stimulation data have been recorded, follow the instructions to analyse these. Otherwise, select Go straight to create MEM file option to create a MEM file. Click OK to continue.
10. Click Save and Exit to continue.
11. Click OK to add the RMC data to MEM file.
12. Click Add from Input RMC file to add this data to the MEM file, then change the directory to save the composite MEM file. Then, click Save and Exit to save it.
13. Click OK to save the remeasured QZD file to allow differentiation from the original QZD file using a # sign.

Results

The following results were obtained in a subgroup of patients from a recent study²², in which there were fibs/psws in all sites showing profuse denervation activity. The results showed that changes in muscle fibers after denervation were assessed in vivo using the MVRC technique described in this protocol. MVRCs showed changes consistent with depolarization of the resting membrane potential in the neurogenic muscle fibers.

Fourteen patients were compared with 29 healthy...

Discussion

MVRCs, as programmed in the recording software, is a highly automated procedure, but care is needed to obtain reliable results. In the recording stage, while adjusting the needles, it is important to avoid stimulating the end-plate zone or nerve. This usually leads to large twitches of the whole muscle, which increases the risk of displacement of the stimulation and/or recording needle during recording MVRCs. To date, the method has been applied to several muscles that have better described end-plate zone; however, the e...

Materials

Name	Company	Catalog Number	Comments
50 Hz Noise Eliminator	Digitimer Ltd		Humbug
Analogue-to-Digital Converter	National Instruments		NI-6221
Analysing software program	Digitimer Ltd (copyright Institute of Neurology, University College, London)		QtracP, MANAL9
Disposable concentric needle electrode, 25 mm x 30G	Natus		Dantec DCN
Disposable monopolar needle electrode, 25 mm x 26G	Natus		TECA elite
Isolated EMG amplifier	Digitimer Ltd		D440
Isolated linear bipolar constant-current stimulator	Digitimer Ltd		DS5
Software and recording protocol	Digitimer Ltd (copyright Institute of Neurology, University College, London)		QtracW software, M3REC3 recording protocol written by Hugh Bostock, Istitute of Neurology, London, UK)