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大鼠的最后区与心血管调节

Area postrema and cardiovascular regulation in rats.

作者信息

Skoog K M, Mangiapane M L

机构信息

Department of Pharmacology, School of Medicine and Dentistry, University of Rochester, New York 14642.

出版信息

Am J Physiol. 1988 May;254(5 Pt 2):H963-9. doi: 10.1152/ajpheart.1988.254.5.H963.

Abstract

The area postrema (AP) of the dog mediates pressor responses to angiotensin II and plays a role in the maintenance of normal arterial pressure. Ablation of the AP (APX) in the rat has been reported to have little or no effect on cardiovascular regulation. In the present study, computer data acquisition techniques were used to investigate this question. APX in the rat significantly lowered resting mean arterial pressure within 1 h (P less than 0.005) and lowered heart rate within 1 day (P less than 0.05) following the lesion. Increases in heart rate following atropine injections were significantly greater (P less than 0.05) in AP relative to sham lesion rats, suggesting higher vagal tone in the AP lesion rats. In addition, APX significantly enhanced the baroreflex control of heart rate in response to intravenous phenylephrine (P less than 0.05). Lability of pressure was not affected by the lesion. The hypotension and bradycardia produced by APX were still present 1 wk after APX. These AP lesions apparently did not produce significant damage to the function of the nearby NTS, since 1) histological analysis revealed minimal NTS damage, 2) arterial pressure lability was not increased, and 3) APX enhanced rather than impaired baroreflex control of heart rate. We conclude that the AP may have a role in the maintenance of resting arterial pressure and heart rate in the rat.

摘要

犬的最后区(AP)介导对血管紧张素II的升压反应,并在维持正常动脉血压中发挥作用。据报道,大鼠的最后区切除(APX)对心血管调节几乎没有影响或没有影响。在本研究中,使用计算机数据采集技术来研究这个问题。大鼠的APX在损伤后1小时内显著降低静息平均动脉压(P<0.005),并在1天内降低心率(P<0.05)。相对于假损伤大鼠,APX大鼠注射阿托品后心率增加显著更大(P<0.05),表明AP损伤大鼠的迷走神经张力更高。此外,APX显著增强了对静脉注射去氧肾上腺素的心率压力反射控制(P<0.05)。压力的不稳定性不受损伤影响。APX产生的低血压和心动过缓在APX后1周仍然存在。这些AP损伤显然没有对附近的孤束核(NTS)功能造成显著损害,因为1)组织学分析显示NTS损伤最小,2)动脉血压不稳定性没有增加,3)APX增强而不是损害心率的压力反射控制。我们得出结论,AP可能在维持大鼠的静息动脉血压和心率中起作用。

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