Clark K E, Mills E G, Harrington D J
Proc Soc Exp Biol Med. 1984 Apr;175(4):476-82. doi: 10.3181/00379727-175-41823.
Histamine H1 and H2 receptors are known to exist in uterine smooth muscle; however, neither receptor has been clearly identified in the uterine vasculature. In the present study, 12 nonpregnant ewes were chronically instrumented with catheters in the carotid artery, jugular vein, uterine arteries, and electromagnetic flow probes on the uterine arteries for continuous measurement of uterine blood flow. Dose response curves were determined for bolus injections of Histamine (1-10 micrograms), the H1 receptor agonist 2PEA (10-100 micrograms), and the H2 receptor agonist Dimaprit (30-300 micrograms) before H1 receptor blockade with pyrilamine, following H1 receptor blockade, and following H2 receptor blockade with metiamide. Uterine vasodilator responses to histamine and 2PEA were essentially abolished by pyrilamine, while responses to dimaprit were not altered. Following addition of metiamide, responses to histamine were reduced further and responses to dimaprit were abolished. Baseline uterine blood flow was not altered by either H1 or H2 receptor blockade or their combination. Intraarterial bolus injections of the mast cell histamine-releasing compound 48/80 (100-1000 micrograms) had no effect on uterine blood flow. These experiments demonstrate that the uterine vasculature of the ovine contains almost exclusively H1 receptors, does not contain compound 48/80 sensitive mast cells and is not dependent upon endogenous histamine to maintain blood flow.
已知组胺H1和H2受体存在于子宫平滑肌中;然而,在子宫血管系统中尚未明确鉴定出这两种受体。在本研究中,对12只未怀孕的母羊进行长期插管,在颈动脉、颈静脉、子宫动脉中插入导管,并在子宫动脉上安装电磁流量探头,以连续测量子宫血流量。在使用吡苄明阻断H1受体之前、阻断H1受体之后以及使用甲硫咪特阻断H2受体之后,分别测定组胺(1 - 10微克)、H1受体激动剂2PEA(10 - 100微克)和H2受体激动剂二甲双胍(30 - 300微克)推注给药的剂量反应曲线。子宫对组胺和2PEA的血管舒张反应基本上被吡苄明消除,而对二甲双胍的反应未改变。加入甲硫咪特后,对组胺的反应进一步降低,对二甲双胍的反应被消除。H1或H2受体阻断或其联合应用均未改变子宫血流量基线。动脉内推注肥大细胞组胺释放化合物48/80(100 - 1000微克)对子宫血流量无影响。这些实验表明,绵羊的子宫血管系统几乎只含有H1受体,不含有对48/80敏感的肥大细胞,并且不依赖内源性组胺来维持血流量。