Related Experiment Videos
Inability of insulin to maintain normal nerve function during high-frequency stimulation in diabetic rat tail nerves
H Andersen1, J F Nielsen, V K Nielsen
1Department of Neurophysiology, Arhus University Hospital, Denmark.
Muscle & Nerve
|January 1, 1994
Summary
Insulin treatment preserves resting nerve function in diabetic rats but fails to prevent nerve dysfunction under high-frequency stimulation. This highlights potential issues in managing diabetic peripheral neuropathy.
Area of Science:
- Neuroscience
- Endocrinology
- Diabetology
Background:
- Diabetic peripheral neuropathy is a common complication of diabetes mellitus.
- Nerve dysfunction in diabetes affects nerve conduction velocity (NCV) and amplitude.
- The role of insulin in preserving nerve function under physiological stress is not fully understood.
Purpose of the Study:
- To investigate the effect of insulin on nerve function in acute experimental diabetes.
- To assess nerve response to long-term high-frequency stimulation (HFS) in diabetic rats with and without insulin treatment.
Main Methods:
- Acute diabetes was induced in rats using streptozotocin.
- Mixed tail nerves were subjected to long-term high-frequency stimulation (143 Hz for 20 min).
- Nerve conduction velocity (NCV) and peak-to-peak amplitude (P-Pamp) were measured in untreated and insulin-treated diabetic rats.
Main Results:
- Untreated diabetic rats exhibited decreased NCV and P-Pamp, with augmented P-Pamp depression during HFS.
- Insulin-treated rats maintained normal resting NCV and P-Pamp but showed similar P-Pamp depression during HFS as untreated rats.
- Insulin preserved resting nerve function but not functional capacity under HFS stress.
Conclusions:
- Insulin treatment in acute experimental diabetes preserves normal resting nerve conduction but does not prevent functional impairment during high-frequency stimulation.
- Axon membrane functional capacity under stress is compromised in diabetes, even with insulin therapy.
- Monitoring axon membrane function may be clinically relevant for managing peripheral neuropathies in diabetic patients.