The trophic influence of tetrodotoxin‐inactive nerves on normal and reinnervated rat skeletal muscles.

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Abstract
Nerve impulses in the rat sciatic nerve were blocked for long periods by tetrodotoxin (TTX) released from capillary implants. The TTX capillaries did not block axonal transport, nor did they cause any sign of nerve degeneration. A comparison of the effects of TTX paralysis and denervation was made on both extensor digitorum longus (e.d.l.) and soleus muscles over 21 days, a time when the products of nerve degeneration were unlikely to contribute to the changes associated with denervation. The resting membrane potential of TTX-paralysed muscles was significantly different (P < 0.005) from that of the denervated muscles at all periods and at 21 days the decrease that can be attributed to inactivity was 61% (e.d.l.) and 49% (soleus) of that which follows denervation. This disparity was more pronounced for the ACh [acetylcholine] receptor density where the increase in receptors due to inactivity was only 34% (e.d.l.) and 21% (soleus) of that due to denervation. A similar comparison was made on muscles which had been reinnervated by TTX-inactive nerves. These muscles had a significantly higher resting membrane potential and lower ACh receptor density than the denervated muscles (P < 0.05). The experiments on reinnervated muscles preclude the possibility that nerve degeneration products are solely responsible for the difference between the TTX-paralysed and denervated muscles and suggest that the difference can be attributed to the trophic influence of the nerve. An observed increase in the m.e.p.p. [miniature end plate potential] frequency of the TTX-paralysed muscles indicated that nerve action potentials play a role in regulating the spontaneous release from nerve terminals.

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