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异丙肾上腺素和福斯高林可增加大鼠垂体诱发的血管加压素释放。

Isoprenaline and forskolin increase evoked vasopressin release from rat pituitary.

作者信息

Racké K, Rothländer M, Muscholl E

出版信息

Eur J Pharmacol. 1982 Aug 13;82(1-2):97-100. doi: 10.1016/0014-2999(82)90560-x.

DOI:10.1016/0014-2999(82)90560-x
PMID:6889972
Abstract

Isolated neurointermediate lobes of rat pituitaries were incubated in Krebs solution. The vasopressin release evoked by electrical stimulation (0.2 ms, 80 V, 15 Hz, 10 s trains at 10 s intervals for a total of 10 min) was completely inhibited by tetrodotoxin. Isoprenaline increased the evoked vasopressin release to a maximum of 60% (EC50 10 nM) and this effect was antagonized surmountably by propranolol. Forskolin increased the vasopressin release by 98%. These results suggest the presence within the neurohypophysis of a beta-adrenoceptor-linked adenylate cyclase facilitating vasopressin secretion.

摘要

将大鼠垂体的孤立神经中间叶置于 Krebs 溶液中进行孵育。电刺激(0.2 毫秒,80 伏,15 赫兹,每隔 10 秒进行 10 秒的刺激串,共持续 10 分钟)诱发的加压素释放被河豚毒素完全抑制。异丙肾上腺素可将诱发的加压素释放增加至最大 60%(半数有效浓度为 10 纳摩尔),且普萘洛尔可有效拮抗此效应。福斯高林使加压素释放增加了 98%。这些结果表明,神经垂体中存在一种与β-肾上腺素能受体相连的腺苷酸环化酶,可促进加压素分泌。

相似文献

1
Isoprenaline and forskolin increase evoked vasopressin release from rat pituitary.异丙肾上腺素和福斯高林可增加大鼠垂体诱发的血管加压素释放。
Eur J Pharmacol. 1982 Aug 13;82(1-2):97-100. doi: 10.1016/0014-2999(82)90560-x.
2
Forskolin: its effects on potassium-evoked release of vasopressin from the rat neurohypophysis.福司可林:其对大鼠神经垂体中钾诱导的血管加压素释放的影响。
Br J Pharmacol. 1985 May;85(1):197-203. doi: 10.1111/j.1476-5381.1985.tb08847.x.
3
Forskolin inhibits potassium-evoked release of vasopressin from rat neurohypophyses.
Naunyn Schmiedebergs Arch Pharmacol. 1985 Jan;328(3):358-60. doi: 10.1007/BF00515568.
4
Facilitation by forskolin of electrically evoked vasopressin release in vitro requires bursting pattern of stimulation.
Brain Res. 1989 May 29;488(1-2):260-4. doi: 10.1016/0006-8993(89)90716-6.
5
The effect of naloxone on vasopressin release from rat neurohypophysis incubated in vitro.纳洛酮对体外培养的大鼠神经垂体释放血管加压素的影响。
J Physiol. 1983 Aug;341:507-15. doi: 10.1113/jphysiol.1983.sp014820.
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Modulation by fenoldopam (SKF 82526) and bromocriptine of the electrically evoked release of vasopressin from the rat neurohypophysis. Effects of dopamine depletion.非诺多泮(SKF 82526)和溴隐亭对大鼠神经垂体电诱发血管加压素释放的调节作用。多巴胺耗竭的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1986 Apr;332(4):332-7. doi: 10.1007/BF00500083.
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Effects of gadolinium and cadmium on the electrically evoked release of 45calcium from the isolated rat neurohypophysis.钆和镉对离体大鼠神经垂体电诱发的45钙释放的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Mar;337(3):301-7. doi: 10.1007/BF00168843.
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Interleukin-1 beta stimulates the release of vasopressin from rat neurohypophysis.
Eur J Pharmacol. 1989 Nov 21;171(2-3):233-5. doi: 10.1016/0014-2999(89)90112-x.
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Endogenous opioid inhibition of the release of oxytocin from the isolated rat neurohypophysis during high-frequency stimulation of the pituitary stalk.在垂体柄高频刺激期间内源性阿片类物质对离体大鼠神经垂体中催产素释放的抑制作用。
Neurosci Lett. 1988 Sep 23;92(1):114-8. doi: 10.1016/0304-3940(88)90752-5.
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Naloxone increases vasopressin secretion from the neurointermediate lobe of the hypophysis of the rat: search for the endogenous agonist.
Life Sci. 1983;33 Suppl 1:499-502. doi: 10.1016/0024-3205(83)90550-7.

引用本文的文献

1
Forskolin and the release of noradrenaline in cerebrocortical slices.福斯高林与大脑皮质切片中去甲肾上腺素的释放
Naunyn Schmiedebergs Arch Pharmacol. 1984 Jan;325(1):17-24. doi: 10.1007/BF00507049.
2
Forskolin: its effects on potassium-evoked release of vasopressin from the rat neurohypophysis.福司可林:其对大鼠神经垂体中钾诱导的血管加压素释放的影响。
Br J Pharmacol. 1985 May;85(1):197-203. doi: 10.1111/j.1476-5381.1985.tb08847.x.
3
Forskolin inhibits potassium-evoked release of vasopressin from rat neurohypophyses.
Naunyn Schmiedebergs Arch Pharmacol. 1985 Jan;328(3):358-60. doi: 10.1007/BF00515568.
4
Modulation by fenoldopam (SKF 82526) and bromocriptine of the electrically evoked release of vasopressin from the rat neurohypophysis. Effects of dopamine depletion.非诺多泮(SKF 82526)和溴隐亭对大鼠神经垂体电诱发血管加压素释放的调节作用。多巴胺耗竭的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1986 Apr;332(4):332-7. doi: 10.1007/BF00500083.