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催乳素对大鼠血压及心血管反应性的影响。

Effect of prolactin on blood pressure and cardiovascular responsiveness in the rat.

作者信息

Mills D E, Ward R P

出版信息

Proc Soc Exp Biol Med. 1986 Jan;181(1):3-8. doi: 10.3181/00379727-181-42217.

Abstract

The effects of chronic ovine PRL (oPRL) infusion on resting systolic blood pressure (BP), heart rate, and pressor responsiveness to acute administration of norepinephrine and angiotensin were studied in adult male Sprague-Dawley rats. oPRL was administered over 7 days, via osmotic pump implanted ip on Day 1, at rates of 0, 0.15, 0.30, 0.60, 1.20, and 4.80 micrograms/hr. Resting BP and heart rate were indirectly determined in conscious rats by tail cuff technique on Days 1, 4, and 7 following pump implantation. In addition, acute pressor responses to ia norepinephrine (4.3 micrograms) and angiotensin (1.25 micrograms) were directly measured via arterial cannula in halothane-anesthetized rats on Day 7 of oPRL administration. oPRL infusion did not alter resting BP or heart rate over the 7 days. However, oPRL increased the BP response to norepinephrine at infusion rates of 0.60 and 4.80 micrograms/hr (P less than 0.01 vs controls). Body weight increases during the study were also greater in groups receiving 0.15, 0.30, 0.60, and 4.80 micrograms oPRL/hr (P less than 0.05) than those in control animals. oPRL decreased pressor responses to angiotensin at infusion rates of 0.30 and 1.20 micrograms/hr (P less than 0.01). These data suggest that, although the vascular effects of oPRL may not be evident under resting conditions, oPRL enhances vascular reactivity to norepinephrine infusion and depresses vascular reactivity to angiotensin infusion. Furthermore, at oPRL infusion rates which affect pressor responses to norepinephrine, oPRL increases body weight gain. These findings support a role for PRL in cardiovascular regulation during conditions of altered sympathetic activity.

摘要

在成年雄性斯普拉格-道利大鼠中,研究了慢性输注绵羊催乳素(oPRL)对静息收缩压(BP)、心率以及对急性给予去甲肾上腺素和血管紧张素的升压反应性的影响。oPRL通过在第1天经腹腔植入的渗透泵给药7天,给药速率分别为0、0.15、0.30、0.60、1.20和4.80微克/小时。在植入泵后的第1、4和7天,通过尾套技术间接测定清醒大鼠的静息血压和心率。此外,在给予oPRL的第7天,在氟烷麻醉的大鼠中通过动脉插管直接测量对静脉注射去甲肾上腺素(4.3微克)和血管紧张素(1.25微克)的急性升压反应。在7天内,oPRL输注未改变静息血压或心率。然而,oPRL在输注速率为0.60和4.80微克/小时时增加了对去甲肾上腺素的血压反应(与对照组相比,P<0.01)。在研究期间,接受0.15、0.30、0.60和4.80微克oPRL/小时的组的体重增加也大于对照组动物(P<0.05)。oPRL在输注速率为0.30和1.20微克/小时时降低了对血管紧张素的升压反应(P<0.01)。这些数据表明,尽管oPRL的血管效应在静息条件下可能不明显,但oPRL增强了对去甲肾上腺素输注的血管反应性,并降低了对血管紧张素输注的血管反应性。此外,在影响对去甲肾上腺素升压反应的oPRL输注速率下,oPRL增加体重增加。这些发现支持了催乳素在交感神经活动改变条件下心血管调节中的作用。

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