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胃动素在人体中的药代动力学。

Pharmacokinetics of motilin in man.

作者信息

Mitznegg P, Bloom S R, Domschke W, Domschke S, Wuensch E, Demling L

出版信息

Gastroenterology. 1977 Mar;72(3):413-6.

PMID:832789
Abstract

The study provides pharmacokinetic data for exogenous synthetic and endogenous natural motilin in man. Synthetic 13-norleucine-motilin was infused into 6 healthy volunteers at a dose of 0.6 and 2.4 (pmoles per kg) per min over 60 min and plasma motilin was measured by radioimmunoassay. During the infusions mean plasma levels of 124.8 +/- 14.8 and 360 +/- 19.6 pmoles per liter, respectively, were achieved. Disappearance half-time on stopping the infusion was 4.36 min. The apparent volume of distribution was calculated to be 49.4 +/- 3.3 ml per kg, and the metabolic clearance rate was 7.8 +/- 0.5 (ml per kg) per min. To measure the decay of endogenous motilin somatostatin was used in the same 6 subjects. A bolus of 100 mug and a subsequent 15-min infusion of 15 mug per min of somatostatin suppressed the fasting motilin level by 50%. The disappearance half-time was 4.56 min. It is concluded that both synthetic and endogenous motilin are eliminated by first order kinetics with very similar half-times. Our data also suggest that the previously reported motilin infusions at these dose levels gave plasma concentrations within the physiological range and that the effects noted may thus have reflected the physiological actions of motilin.

摘要

该研究提供了人体中外源性合成胃动素和内源性天然胃动素的药代动力学数据。将合成的13-去甲亮氨酸-胃动素以每分钟0.6和2.4(皮摩尔/千克)的剂量输注给6名健康志愿者,持续60分钟,并通过放射免疫测定法测量血浆胃动素。在输注过程中,平均血浆水平分别达到每升124.8±14.8和360±19.6皮摩尔。停止输注后的消失半衰期为4.36分钟。计算得出表观分布容积为每千克49.4±3.3毫升,代谢清除率为每分钟7.8±0.5(毫升/千克)。为了测量内源性胃动素的衰减,对相同的6名受试者使用了生长抑素。静脉注射100微克生长抑素,随后以每分钟15微克的速度输注15分钟,可使空腹胃动素水平降低50%。消失半衰期为4.56分钟。结论是,合成胃动素和内源性胃动素均通过一级动力学消除,半衰期非常相似。我们的数据还表明,先前报道的这些剂量水平的胃动素输注产生了生理范围内的血浆浓度,因此所观察到的效应可能反映了胃动素的生理作用。

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