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小鼠血管纹中腺苷酸环化酶的激素调节

Hormonal regulation of adenylate cyclase in the stria vascularis of the mouse.

作者信息

Schacht J

出版信息

Hear Res. 1985;20(1):9-13. doi: 10.1016/0378-5955(85)90053-x.

Abstract

The adenylate cyclase complex is a ubiquitous 'second-messenger' system mediating the actions of hormones and neurotransmitters. Its presence but not its physiological control and function had previously been established in the cochlea. In this study, the hormonal stimulation of adenylate cyclase activity of the stria vascularis of the CBA mouse was characterized. In the presence of the regulatory nucleotide, GTP, the enzyme was stimulated by isoproterenol and epinephrine with a half-maximal effect at about 10 microM and the stimulation was blocked by propranolol. This profile is consistent with the presence of adrenergic beta 2-receptors on the strial enzyme complex. Hormones and neuromodulators preferring other receptor subtypes were ineffective; the non-specific stimulator, forskolin, activated the enzyme. The finding that potential hormonal effectors of water and ion transport including vasopressin were inactive may be significant with regard to the physiological role of strial adenylate cyclase.

摘要

腺苷酸环化酶复合物是一种普遍存在的“第二信使”系统,介导激素和神经递质的作用。此前已在耳蜗中证实了它的存在,但尚未明确其生理调控及功能。在本研究中,对CBA小鼠血管纹腺苷酸环化酶活性的激素刺激特性进行了表征。在调节性核苷酸GTP存在的情况下,异丙肾上腺素和肾上腺素可刺激该酶,半最大效应浓度约为10微摩尔,且这种刺激可被普萘洛尔阻断。这一特征与血管纹酶复合物上存在肾上腺素能β2受体相一致。偏好其他受体亚型的激素和神经调节剂无效;非特异性刺激剂福司可林可激活该酶。包括血管加压素在内的水和离子转运的潜在激素效应物无活性这一发现,可能对血管纹腺苷酸环化酶的生理作用具有重要意义。

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