Neuropathy in the spontaneously hypertensive rat: An electrophysiological and histological study.

INTRODUCTION: Hypertension is identified as a risk factor for development of polyneuropathy. In this study we examined nerve conduction and morphological alteration of peripheral nerves in spontaneously hypertensive rats (SHR). METHODS: Motor nerve conduction velocity (MNCV) in the sciatic-tibial nerve and sensory nerve conduction velocity (SNCV) in the sural nerve were measured. Pathological investigations included spinal cord, dorsal root ganglion, and hindlimb nerves in SHR and Wistar-Kyoto rats (WKY) aged 4-64 weeks. RESULTS: Blood pressure was significantly higher in SHR than WKY animals at 4 weeks and elevated further with aging. MNCV and SNCV were significantly slower in SHR compared with WKY after age 24 weeks. Prominent morphological changes in SHR nerves included axonal atrophy and myelin splitting. SHR also had endoneurial microangiopathy with reduplication of basement membrane. CONCLUSIONS: SHR showed slowed nerve conduction velocity and pathological abnormalities of hindlimb nerves. Sustained severe hypertension may cause axonal atrophy and endoneurial microangiopathy. Muscle Nerve 54: 756-762, 2016.

A rat model of Urtica ferox neuropathy.

A species of stinging nettle, Urtica ferox, is indigenous to New Zealand and has caused deaths in animals and humans. We previously reported a human case of acute polyneuropathy due to U. ferox stings. We developed an experimental animal model of U. ferox toxin neuropathy to determine its neurophysiological and pathological characteristics. Male Wistar rats received either normal saline or fluid from U. ferox trichomes by injection into the epineurium of the left sciatic nerve. Neurophysiological and histological studies were carried out 5, 14 and 28 days after administration. Toxin-injected rats developed paresis of the left leg by 14 days with recovery by 28 days. Compound muscle action potentials amplitudes on the left side of toxin-administered rats at day 14 were significantly reduced compared to the right uninjected side. Toxin-injected nerves at days 5 and 14 showed a reduction in the number of myelinated fibres compared to the saline-injected nerves and frequency distributions of myelinated fibres showed a shift to smaller fibres. U. ferox neurotoxin thus produced a transient neuropathy in rat peripheral nerves with neurophysiological and pathological features suggestive of axonopathy. The identity and mechanism of action of the toxin responsible for neuropathy are uncertain.

Prolonged ischemic conduction failure after reperfusion in diabetic nerve.

Diabetic nerve exhibits morphological vulnerability to ischemia and reperfusion, in contrast to its physiological resistance to ischemic conduction failure (RICF). To examine the sequence of ischemic conduction failure after reperfusion in diabetic nerve, we measured sciatic-tibial nerve conduction before and during 30-180 min of ischemia and after reperfusion for up to 1 week in streptozocin (STZ)-induced diabetic rats. RICF in diabetic rats was confirmed during ischemia. After reperfusion, control nerves showed an immediate recovery in amplitude of compound muscle action potential (CMAP) following ischemia for 120 min or less, and delayed recovery after 150 min of ischemia. In contrast, recovery in diabetic nerves was delayed even after 1 h of ischemia. Ischemia for 75 min in diabetic nerve resulted in either delayed or no recovery of the CMAP upon reperfusion. Following ischemia for 90 or 120 min, axonal degeneration was observed in diabetic nerve. Thus, severe ischemia for 60 or 75 min causes prolonged ischemic conduction failure in diabetic nerve, compared with 150 min in control nerve. In conclusion, diabetic nerve shows delayed recovery of ischemic conduction failure after brief ischemia, compared to controls, suggesting that patients with diabetic neuropathy have a worse prognosis when faced with nerve ischemia.