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神经肽Y通过百日咳毒素敏感的G蛋白抑制β-肾上腺素能激动剂和血管活性肠肽诱导的大鼠松果体细胞中环磷酸腺苷的积累。

Neuropeptide Y inhibits beta-adrenergic agonist- and vasoactive intestinal peptide-induced cyclic AMP accumulation in rat pinealocytes through pertussis toxin-sensitive G protein.

作者信息

Harada Y, Okubo M, Yaga K, Kaneko T, Kaku K

机构信息

Third Department of Internal Medicine, Yamaguchi University School of Medicine, Ube, Japan.

出版信息

J Neurochem. 1992 Dec;59(6):2178-83. doi: 10.1111/j.1471-4159.1992.tb10109.x.

Abstract

The effects of neuropeptide Y (NPY) on pineal gland cyclic AMP (cAMP) accumulation were investigated using dispersed pinealocytes from rats. NPY inhibited the intracellular cAMP accumulation stimulated by isoproterenol and norepinephrine in a dose-dependent manner during a 10-min incubation of pinealocytes. NPY (1 x 10(-7) M) also inhibited vasoactive intestinal peptide (VIP)- and cholera toxin-induced cAMP accumulation. The inhibitory effect of NPY on isoproterenol-induced cAMP accumulation was completely abolished by a 5-h pretreatment of pinealocytes with 1 microgram/ml of pertussis toxin (PT). These results suggest that NPY participates in modulation of cAMP production in the rat pineal gland through PT-sensitive G protein. Yohimbine, an alpha 2-adrenergic antagonist, blocked NPY inhibition of isoproterenol-stimulated cAMP accumulation. On the other hand, the alpha 2-adrenergic agonist clonidine by itself did not affect cAMP accumulation stimulated by isoproterenol but significantly potentiated NPY action. The present study demonstrates that NPY inhibits beta-adrenergic or VIPergic stimulation of the pineal gland cAMP accumulation. The inhibitory effect of NPY is mediated through PT-sensitive G protein. Our results also suggest that NPY exerts its action to affect alpha 2-adrenoceptor function.

摘要

利用大鼠的松果体分散细胞,研究了神经肽Y(NPY)对松果体环磷酸腺苷(cAMP)积累的影响。在松果体细胞孵育10分钟期间,NPY以剂量依赖的方式抑制异丙肾上腺素和去甲肾上腺素刺激的细胞内cAMP积累。NPY(1×10⁻⁷M)也抑制血管活性肠肽(VIP)和霍乱毒素诱导的cAMP积累。用1微克/毫升百日咳毒素(PT)对松果体细胞进行5小时预处理后,NPY对异丙肾上腺素诱导的cAMP积累的抑制作用完全消除。这些结果表明,NPY通过PT敏感的G蛋白参与大鼠松果体中cAMP产生的调节。α₂肾上腺素能拮抗剂育亨宾可阻断NPY对异丙肾上腺素刺激的cAMP积累的抑制作用。另一方面,α₂肾上腺素能激动剂可乐定本身并不影响异丙肾上腺素刺激的cAMP积累,但能显著增强NPY的作用。本研究表明,NPY抑制松果体cAMP积累的β肾上腺素能或VIP能刺激。NPY的抑制作用是通过PT敏感的G蛋白介导的。我们的结果还表明,NPY通过影响α₂肾上腺素能受体功能发挥其作用。

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