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肾上腺素能药物和去神经支配对大鼠松果体中血清素N-乙酰基转移酶的诱导和超诱导作用

Induction and superinduction of serotonin N-acetyltransferase by adrenergic drugs and denervation in rat pineal organ.

作者信息

Deguchi T, Axelrod J

出版信息

Proc Natl Acad Sci U S A. 1972 Aug;69(8):2208-11. doi: 10.1073/pnas.69.8.2208.

Abstract

Activity of serotonin N-acetyltransferase (EC 2.3.1.5) in rat pineal organ is rapidly and markedly elevated in vivo after administration of beta-(3,4-dihydroxyphenyl)-L-alanine (L-DOPA), norepinephrine, epinephrine, isoproterenol, monoamine oxidase inhibitors, or theophylline. Serotonin or 5-hydroxytryptophan has no effect on the increase in activity of this enzyme. Inhibitors of protein synthesis or propranolol, a beta-adrenergic blocking agent completely inhibit(s) the increase in activity of serotonin N-acetyltransferase induced by drugs, indicating that new enzyme molecules are formed via stimulation of beta-receptors of pineal cells and adenosine 3':5'-cyclic monophosphate. When rat pineal organ is denervated by ganglionectomy, beta-(3,4-dihydroxyphenyl)-L-alanine induces much more serotonin N-acetyltransferase than in the innervated gland. This superinduction by denervation appears to be due to changes of the postsynaptic site, probably the beta-adrenergic receptor on the pineal cell.

摘要

给予β-(3,4-二羟基苯基)-L-丙氨酸(L-多巴)、去甲肾上腺素、肾上腺素、异丙肾上腺素、单胺氧化酶抑制剂或茶碱后,大鼠松果体器官中血清素N-乙酰基转移酶(EC 2.3.1.5)的活性在体内迅速且显著升高。血清素或5-羟色氨酸对该酶活性的增加没有影响。蛋白质合成抑制剂或β-肾上腺素能阻断剂普萘洛尔完全抑制药物诱导的血清素N-乙酰基转移酶活性的增加,表明新的酶分子是通过刺激松果体细胞的β-受体和3':5'-环磷酸腺苷形成的。当通过神经节切除术使大鼠松果体器官去神经支配时,β-(3,4-二羟基苯基)-L-丙氨酸诱导的血清素N-乙酰基转移酶比在有神经支配的腺体中多得多。这种去神经支配后的超诱导似乎是由于突触后位点的变化,可能是松果体细胞上的β-肾上腺素能受体的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/426901/1ac0db493ce1/pnas00134-0220-a.jpg

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