کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4335149 | 1295126 | 2012 | 7 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Electrophysiological features of the mouse tail nerves and their changes in chemotherapy induced peripheral neuropathy (CIPN) Electrophysiological features of the mouse tail nerves and their changes in chemotherapy induced peripheral neuropathy (CIPN)](/preview/png/4335149.png)
Electrophysiology of tail nerves in rodents has been demonstrated a reliable method to investigate models of peripheral neuropathies. Nevertheless, data concerning mouse models are lacking. We assessed the normal features of sensory and motor conduction of tail nerves in adult mice. We found that, as in rats, a sensory compound action potential and motor responses could be recorded with the non invasive and highly reliable technique proposed, especially if bipolar derivations were used. We also investigated the changes related to chemotherapy induced peripheral neuropathy (CIPN) after paclitaxel treatment (times 1 and 2), compared to pre-treatment (time 0) and to controls. It was found that only the sensory compound action potential was involved in CIPN, with decrease in amplitude and conduction velocity, suggesting a significant reduction in number of fast conducting fibres and a correspondent increase in the number of slow conducting ones, although the total amount of active myelinated fibres was deemed to be unchanged through time 0, time 1 and time 2. The results obtained in CIPN provide new functional evidence about the involvement of sensory fibres and may help in better understanding the underlying mechanisms.
► Sensory compound action potentials can be recorded from mouse tail nerves.
► Motor potentials can be recorded as well from the same nerves.
► The two types of potentials were used to study chemotherapy induced peripheral neuropathy.
► Neuropathic nerves showed a decrease of conduction velocity in all sensory fibres.
► Although slowed down, the total amount of functioning axons was not changed.
Journal: Journal of Neuroscience Methods - Volume 209, Issue 2, 15 August 2012, Pages 403–409