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灵长类动物胆囊中的组胺受体。

Histamine receptors in primate gallbladder.

作者信息

Schoetz D J, Wise W E, La Morte W W, Birkett D H, Williams L F

出版信息

Dig Dis Sci. 1983 Apr;28(4):353-8. doi: 10.1007/BF01324954.

Abstract

The effect of intravenous histamine on intragallbladder pressure (GBp) and subsequent modification of the histamine response by H1- and H2-antagonists was investigated in an awake baboon model. Responses to specific H1- and H2-agonists were also examined in order to further elucidate gallbladder histamine responses. Gallbladder volume (GBv) was arbitrarily set at 60-70% of observed resting GBv, and drugs were then infused intravenously with continuous monitoring of GBp. Histamine administration resulted in a logarithmic dose--response curve with a maximal increase in GBp equal to 31.7 mm Hg at a dose of 0.0625 mg of histamine. Infusion of the H1-antagonist diphenhydramine hydrochloride (Benadryl) resulted in a decreased GBp response to histamine when compared to preblocker response at all doses studied. On the other hand, histamine response following administration of the H2-antagonist metiamide was significantly greater than the preblocker histamine response. Infusion of the H1-agonist 2-pyridylethlamine resulted in a dose-dependent increase in GBp similar to the histamine curve, while infusion of the H2-agonist dimaprit resulted in consistent decreases in GBp. These results extend previous observations in subprimate preparations and demonstrate the presence of both stimulatory H1-receptors and inhibitory H2-receptors in an in situ primate model.

摘要

在清醒的狒狒模型中,研究了静脉注射组胺对胆囊内压(GBp)的影响以及H1和H2拮抗剂对组胺反应的后续调节作用。还检测了对特定H1和H2激动剂的反应,以进一步阐明胆囊组胺反应。将胆囊容积(GBv)任意设定为观察到的静息GBv的60 - 70%,然后静脉输注药物,并持续监测GBp。给予组胺导致对数剂量 - 反应曲线,在组胺剂量为0.0625 mg时,GBp最大增加量等于31.7 mmHg。在所有研究剂量下,与给予阻滞剂前的反应相比,输注H1拮抗剂盐酸苯海拉明(苯那君)导致对组胺的GBp反应降低。另一方面,给予H2拮抗剂甲硫咪特后的组胺反应明显大于给予阻滞剂前的组胺反应。输注H1激动剂2 - 吡啶乙胺导致GBp呈剂量依赖性增加,类似于组胺曲线,而输注H2激动剂二甲双胍导致GBp持续降低。这些结果扩展了先前在灵长类以下动物制剂中的观察结果,并证明在原位灵长类模型中存在刺激性H1受体和抑制性H2受体。

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