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妊娠期间血管舒张的机制:前列腺素和一氧化氮在妊娠大鼠原位血液灌注肠系膜血管反应性变化中作用的研究

Mechanisms of vasodilatation in pregnancy: studies of the role of prostaglandins and nitric-oxide in changes of vascular reactivity in the in situ blood perfused mesentery of pregnant rats.

作者信息

Chu Z M, Beilin L J

机构信息

University of Western Australia, Department of Medicine, Perth.

出版信息

Br J Pharmacol. 1993 Jun;109(2):322-9. doi: 10.1111/j.1476-5381.1993.tb13573.x.

DOI:10.1111/j.1476-5381.1993.tb13573.x
PMID:8358537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2175702/
Abstract
  1. To examine the possible mechanisms of the vasodilatation and blunted pressor responses in late pregnancy, we have studied vascular reactivity of the in situ blood perfused mesenteric resistance vessels of 18-20 day pregnant Wistar-Kyoto rats (WKY). 2. Intra-arterial mean blood pressure (MBP) was lower in pregnant rats than in nonpregnant controls. There was no significant difference in basal mesenteric perfusion pressure (BPP) between groups. 3. Vascular reactivity to electrical stimulation (ES) or intra-arterial noradrenaline (NA), angiotensin II (AII) and arginine vasopressin (AVP) was decreased in the preparations from pregnant rats compared to that from nonpregnant controls. Noradrenaline spillover into mesenteric venous blood following ES was similar in pregnant and nonpregnant animals. 4. Indomethacin (5 mg kg-1, i.v.), an inhibitor of cyclo-oxygenase, induced significant increases in reactivity to ES in both pregnant and nonpregnant groups while potentiating the responses to NA and AII in nonpregnant animals only and having no effect on AVP-induced contractions in the preparations from either pregnant or nonpregnant animals. 5. NG-nitro-L-arginine (L-NOARG) (5 mg kg-1, i.v.), an inhibitor of nitric-oxide synthase, increased MBP and BPP in both pregnant and nonpregnant animals, but the difference in MBP between groups was still evident. 6. L-NOARG enhanced mesenteric vascular responses to ES, NA and AII in both pregnant and nonpregnant groups. Only the difference in NA responses between groups was abolished after pretreatment with L-NOARG. 7. These data show that vasoconstrictor responses to a variety of agonists are decreased in the in situ blood-perfused mesenteric resistance vessels of pregnant rats. Increase in endothelial-dependent nitric oxide generation could contribute to the vasodilatation seen in pregnancy but other mechanisms might also be involved. Cyclo-oxygenase products are not responsible for any decreased contractile responses in this preparation.
摘要
  1. 为研究妊娠晚期血管舒张及压力反应减弱的可能机制,我们对妊娠18 - 20天的Wistar - Kyoto大鼠(WKY)原位血液灌注的肠系膜阻力血管的血管反应性进行了研究。2. 妊娠大鼠的动脉平均血压(MBP)低于未妊娠对照组。两组间基础肠系膜灌注压(BPP)无显著差异。3. 与未妊娠对照组相比,妊娠大鼠制备物中对电刺激(ES)或动脉内去甲肾上腺素(NA)、血管紧张素II(AII)和精氨酸加压素(AVP)的血管反应性降低。电刺激后去甲肾上腺素溢入肠系膜静脉血在妊娠和未妊娠动物中相似。4. 环氧化酶抑制剂吲哚美辛(5 mg kg-1,静脉注射)在妊娠和未妊娠组中均诱导对电刺激的反应性显著增加,同时仅增强未妊娠动物对NA和AII的反应,对妊娠或未妊娠动物制备物中AVP诱导的收缩无影响。5. 一氧化氮合酶抑制剂NG - 硝基 - L - 精氨酸(L - NOARG)(5 mg kg-1,静脉注射)在妊娠和未妊娠动物中均增加MBP和BPP,但两组间MBP差异仍明显。6. L - NOARG增强妊娠和未妊娠组中肠系膜血管对ES、NA和AII的反应。用L - NOARG预处理后仅消除了两组间对NA反应的差异。7. 这些数据表明,妊娠大鼠原位血液灌注的肠系膜阻力血管对多种激动剂的血管收缩反应降低。内皮依赖性一氧化氮生成增加可能导致妊娠时出现的血管舒张,但也可能涉及其他机制。环氧化酶产物与该制备物中任何收缩反应降低无关。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7ec/2175702/af621b167c5f/brjpharm00719-0046-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7ec/2175702/af621b167c5f/brjpharm00719-0046-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7ec/2175702/af621b167c5f/brjpharm00719-0046-a.jpg

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