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去甲肾上腺素或异丙肾上腺素对大鼠松果体II型甲状腺素5'-脱碘酶活性的体内刺激作用。

In vivo stimulation of rat pineal type II thyroxine 5'-deiodinase activity by either norepinephrine or isoproterenol.

作者信息

Guerrero J M, Santana C, Reiter R J

机构信息

Department of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio 78284-7762.

出版信息

Proc Soc Exp Biol Med. 1990 Sep;194(4):327-31. doi: 10.3181/00379727-194-43099.

Abstract

Herein we show, for the first time, a very marked increase in thyroxine 5'-deiodinase (5'-D) activity in rats injected with norepinephrine (NE) and desmethylimipramine, a drug which inhibits NE uptake by nerve terminals. The response to NE was greater in pineals collected from hypothyroid animals than in glands from euthyroid animals. NE was more effective in stimulating pineal 5'-D than was isoproterenol, suggesting that, in addition to beta-adrenergic receptors, alpha-adrenergic receptors might be involved in the 5'-D activation. However, phenylephrine, an alpha-adrenergic agonist, did not potentiate the effect of isoproterenol on pineal 5'-D activity. The nocturnal increase in pineal 5'-D activity was completely abolished by propranolol, a beta-adrenergic receptor blocker, while prazosin, an alpha-adrenergic receptor blocker, had minimal effect. These results show that the role of alpha-receptors in promoting the NE-mediated rise in rat pineal 5'-D activity is minor in contrast to the role of beta-adrenergic receptors.

摘要

在此,我们首次展示了,在注射去甲肾上腺素(NE)和去甲丙咪嗪(一种抑制神经末梢摄取NE的药物)的大鼠中,甲状腺素5'-脱碘酶(5'-D)活性有非常显著的增加。甲状腺功能减退动物的松果体对NE的反应比甲状腺功能正常动物的腺体更强。NE比异丙肾上腺素更有效地刺激松果体5'-D,这表明除了β-肾上腺素能受体外,α-肾上腺素能受体可能也参与了5'-D的激活。然而,α-肾上腺素能激动剂苯肾上腺素并没有增强异丙肾上腺素对松果体5'-D活性的作用。β-肾上腺素能受体阻滞剂普萘洛尔完全消除了松果体5'-D活性的夜间增加,而α-肾上腺素能受体阻滞剂哌唑嗪的作用极小。这些结果表明,与β-肾上腺素能受体的作用相比,α-受体在促进NE介导的大鼠松果体5'-D活性升高方面的作用较小。

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