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Angiotensin II-induced release of oxytocin: interaction with norepinephrine and role in lactation.

机译:血管紧张素II诱导的催产素释放:与去甲肾上腺素的相互作用以及在泌乳中的作用。

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These studies examined the receptors involved in angiotensin II (Ang II) stimulated secretion of systemic oxytocin (OT) and the role of this peptide in release of OT during suckling. Plasma OT concentrations were measured following intracerebroventricular (icv) injection of vehicle, Ang II, or Ang II following pretreatment with a selective AT1 (Losartan) or AT2 (PD 123319) receptor antagonist. Furthermore, we measured Ang II-induced OT release during central alpha-adrenergic receptor blockade (phentolamine). Finally, plasma OT concentrations before and during suckling were evaluated following central administration of Ang II receptor antagonists. The increase in systemic OT following central Ang II was abolished by AT1 receptor blockade and inhibited by the AT2 receptor antagonist. Furthermore, pretreatment with phentolamine significantly diminished systemic OT release in response to icv Ang II. Finally, central Ang II receptor blockade did not alter the increase in circulating OT during suckling. These data demonstrate that Ang II evoked OT release is mediated through activation of both AT1 and AT2 receptors and suggest that a component of Ang II-induced OT stimulation is due to norepinephrine release. Furthermore, central angiotensin systems do not have a direct role in stimulating OT release during suckling.
机译:这些研究检查了参与血管紧张素II(Ang II)刺激的全身性催产素(OT)分泌的受体,以及该肽在哺乳期间OT释放中的作用。用选择性AT1(Losartan)或AT2(PD 123319)受体拮抗剂预处理脑室内(icv)注射媒介物,Ang II或Ang II后,测量血浆OT浓度。此外,我们测量了中枢α-肾上腺素受体阻滞(酚妥拉明)期间Ang II诱导的OT释放。最后,在集中施用Ang II受体拮抗剂后,评估了在哺乳之前和期间的血浆OT浓度。中枢Ang II后全身性OT的增加被AT1受体阻滞所消除,并被AT2受体拮抗剂抑制。此外,用酚妥拉明预处理可显着减少对icv Ang II的全身性OT释放。最后,中枢Ang II受体阻滞没有改变哺乳期间循环性OT的增加。这些数据表明,Ang II引起的OT释放是通过激活AT1和AT2受体介导的,并表明Ang II诱导的OT刺激的一个成分是由于去甲肾上腺素的释放。此外,中央血管紧张素系统在哺乳期间不具有刺激OT释放的直接作用。

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