Quik M, Weldon P, Collier B
Exp Neurol. 1987 Jan;95(1):178-93. doi: 10.1016/0014-4886(87)90016-1.
We studied the effect of destruction of the adrenergic neuronal population on the recovery of preganglionic choline acetyltransferase activity in adult rat sympathetic ganglia. To produce a partial destruction of the adrenergic system, rats were injected with guanethidine for 4 weeks; the preganglionic nerve to the superior cervical ganglion was then crushed and the guanethidine injections were continued for an additional 3 days to 6 weeks. To determine that the drug was effective, tyrosine hydroxylase activity was assessed; enzymic activity was reduced by 76% or more after guanethidine administration. In addition, electron microscopy studies showed that the number of principal cell-synaptic contacts and vesicle-containing varicosities were decreased by 90% after guanethidine administration. Those measures indicated the drug effectively destroyed the postsynaptic adrenergic neurons. In contrast, crushing the preganglionic nerve in animals not treated with guanethidine did not change tyrosine hydroxylase activity, suggesting minimal nonspecific damage to the ganglion as a result of the lesion. Choline acetyltransferase activity was measured as an index of presynaptic cholinergic integrity. After crush of the preganglionic nerve, there was a gradual recovery of ganglionic choline acetyltransferase activity in the saline-injected rats from 5% of control 3 days after the crush to 49% of control after 6 weeks. On the other hand, in the ganglia of rats administered guanethidine, there was a much enhanced recovery of choline acetyltransferase activity after the nerve crush compared with saline-injected animals; in the guanethidine-injected rats, the ganglionic choline acetyltransferase activity 3 days and 6 weeks after the nerve crush was 15 and 96%, respectively, compared with the uncrushed side. These results demonstrate after destruction of the adrenergic target tissue, recovery of presynaptic choline acetyltransferase activity in the adult rat sympathetic ganglion can still occur after denervation; however, the mechanism(s) that controls the regeneration is altered, so that enzymic activity is enhanced.
我们研究了去甲肾上腺素能神经元群体的破坏对成年大鼠交感神经节节前胆碱乙酰转移酶活性恢复的影响。为了部分破坏去甲肾上腺素能系统,给大鼠注射胍乙啶4周;然后压迫颈上神经节的节前神经,并继续注射胍乙啶3天至6周。为了确定药物是否有效,评估了酪氨酸羟化酶活性;给予胍乙啶后酶活性降低了76%或更多。此外,电子显微镜研究表明,给予胍乙啶后,主要细胞突触接触和含囊泡的曲张体数量减少了90%。这些措施表明该药物有效地破坏了突触后去甲肾上腺素能神经元。相比之下,在未用胍乙啶处理的动物中压迫节前神经并没有改变酪氨酸羟化酶活性,这表明该损伤对神经节的非特异性损伤最小。胆碱乙酰转移酶活性作为突触前胆碱能完整性的指标进行测量。压迫节前神经后,注射生理盐水的大鼠神经节胆碱乙酰转移酶活性逐渐恢复,从压迫后3天的对照值的5%恢复到6周后的对照值的49%。另一方面,在给予胍乙啶的大鼠神经节中,与注射生理盐水的动物相比,神经压迫后胆碱乙酰转移酶活性的恢复明显增强;在注射胍乙啶的大鼠中,神经压迫后3天和6周神经节胆碱乙酰转移酶活性分别为未压迫侧的15%和96%。这些结果表明,去甲肾上腺素能靶组织破坏后,成年大鼠交感神经节在去神经支配后仍可出现突触前胆碱乙酰转移酶活性的恢复;然而,控制再生的机制发生了改变,从而使酶活性增强。