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[器官培养中渗透压力及血管紧张素II对豚鼠下丘脑-神经垂体复合体精氨酸加压素释放的刺激作用(作者译)]

[Osmotic pressure and angiotensin II stimulation of arginine vasopressin release from a guinea pig hypothalamo-neurohypophyseal complex in organ culture (author's transl)].

作者信息

Ishikawa S, Saito T, Yoshida S

出版信息

Nihon Naibunpi Gakkai Zasshi. 1980 Mar 20;56(3):262-73. doi: 10.1507/endocrine1927.56.3_262.

Abstract

An organ culture system of a male guinea pig hypothalamo-neurohypophyseal complex (HNC) was established. On day 5 in culture, (Na+ -K+) ATPase activity was 0.83 +/- 0.11 mM Pi/mg prot/hr (mean +/- SEM): that is 67% of that on day 1 in culture. 3H-thymidine incorporated into DNA in the explants of HNC was 1,205 +/- 185 cpm/microgram DNA. The explants responded to the elevated KCl medium and the hypertonic solution of sodium chloride with a 470 +/- 38% and 298 +/- 31% increase in arginine vasopression (AVP) release, respectively. This response was inhibited by the addition of tetrodotoxin to the culture medium. AVP release from the explants in res-onse to angiotensin II increased significantly in a dose dependent manner. [Sar1, Ile8] angiotensin II, however, attenuated the response of the explants to angiotensin II when administered simultaneously with angiotensin II. These results suggest that angiotensin II and its analogue cause the AVP release from the explants in a competitive manner. The concentrations of AVP in the culture media made hypertonic with sodium chloride, sucrose and mannitol were 298 +/- 31% (p less than 0.01), 251 +/- 36% (p less than 0.01) and 255 +/- 59% (p less than 0.05) of their control values, respectively. The hypertonic solutions of sodium chloride, sucrose and mannitol caused AVP release from the explants in vitro, while the hypertonic solutions of glucose and urea were revealed to be poor osmotic stimuli on AVP release. These results support the concept of osmoreceptors to release AVP from the hypothalamo-neurohypophyseal axis.

摘要

建立了雄性豚鼠下丘脑 - 神经垂体复合体(HNC)的器官培养系统。在培养的第5天,(钠 - 钾)ATP酶活性为0.83±0.11 mM Pi/mg蛋白/小时(平均值±标准误):即培养第1天该活性的67%。HNC外植体中掺入DNA的3H - 胸腺嘧啶核苷为1,205±185 cpm/μg DNA。外植体对高钾培养基和高渗氯化钠溶液的反应分别是精氨酸加压素(AVP)释放增加470±38%和298±31%。向培养基中添加河豚毒素可抑制这种反应。外植体对血管紧张素II的反应中AVP释放呈剂量依赖性显著增加。然而,[Sar1,Ile8]血管紧张素II与血管紧张素II同时给药时,会减弱外植体对血管紧张素II的反应。这些结果表明,血管紧张素II及其类似物以竞争性方式导致外植体释放AVP。用氯化钠、蔗糖和甘露醇使培养基变为高渗时,培养基中AVP的浓度分别为其对照值的298±31%(p<0.01)、251±36%(p<0.01)和255±59%(p<0.05)。氯化钠、蔗糖和甘露醇的高渗溶液在体外可导致外植体释放AVP,而葡萄糖和尿素的高渗溶液对AVP释放的渗透刺激作用较弱。这些结果支持渗透压感受器从下丘脑 - 神经垂体轴释放AVP的概念。

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