The effects of intrathecal morphine and naltrexone on autotomy in sciatic nerve sectioned rats

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Abstract
Rats were implanted with an intrathecal catheter aimed at the lumbar enlargement (LE). Morphine hydrochloride (240 .mu.g/day) was infused continuously on the spinal cord for 14 days with an osmotic minipump delivering 0.5 .mu.l/h solution or a bolus dose of naltrexone (37.5, 75 or 150 .mu.g) was injected intrathecally. Intrathecally infused morphine delivered on the dorsum of the LE induced analgesia, as tested on the hot plate, whereas normal saline was without effect. Naltrexone caused hyperalgesia revealed as decreased threshold for vocalization to electrical stimulation of the tail. Rats with unilaterally sectioned sciatic nerves that were continuously infused with morphine on the dorsum of the LE autotomized significantly less than saline controls. Nerve sectioned rats injected with naltrexone had an overall level of autotomy similar to saline controls. Autotomy had a somewhat earlier onset and was more severe with naltrexone than with saline. Intrathecal infusion of opiates specifically reduces autotomy, a behavior that may occur as a result of chronic discomfort or pain following nerve injury. The endogenous opiate system at the spinal level may be involved in the control of autotomy.