Gutzwiller J P, Drewe J, Hildebrand P, Rossi L, Lauper J Z, Beglinger C
Division of Gastroenterology, University Hospital, Basel, Switzerland.
Gastroenterology. 1994 May;106(5):1168-73. doi: 10.1016/0016-5085(94)90006-x.
BACKGROUND/AIMS: Bombesin and gastrin-releasing peptide (GRP) are closely related peptides. Both have been proposed to serve as a satiety signal in animals.
To explore further the role of GRP in humans, its effects on satiety and eating behavior were investigated by infusion of GRP into healthy men at three dosages (10, 40, and 160 pmol/kg per hour) and compared with saline infusions.
GRP produced a significant reduction in calorie intake (P < 0.05) but only a 19% (nonsignificant) reduction in food intake. Fluid ingestion was not affected by GRP. No overt side effects were produced by GRP, but subjects experienced d less hunger and early fullness in the premeal period during GRP infusion but not when receiving saline (P < 0.05-0.01).
This study shows that intravenous infusions of GRP can decrease spontaneous food intake at concentrations that produce physiological effects, such as stimulation of acid or pancreatic secretion or gallbladder contraction. The data imply that GRP-like peptides can act as satiety signals in humans, confirming data previously reported in animals.
背景/目的:蛙皮素和胃泌素释放肽(GRP)是密切相关的肽类。两者都被认为在动物中作为饱腹感信号起作用。
为了进一步探究GRP在人类中的作用,通过以三种剂量(每小时10、40和160皮摩尔/千克)向健康男性输注GRP来研究其对饱腹感和进食行为的影响,并与输注生理盐水进行比较。
GRP使卡路里摄入量显著降低(P<0.05),但食物摄入量仅降低了19%(无统计学意义)。液体摄入不受GRP影响。GRP未产生明显副作用,但在输注GRP期间的餐前阶段,受试者饥饿感减轻且较早产生饱腹感,而输注生理盐水时则无此现象(P<0.05 - 0.01)。
本研究表明静脉输注GRP能够在产生诸如刺激胃酸或胰腺分泌或胆囊收缩等生理效应的浓度下降低自发食物摄入量。这些数据表明GRP样肽在人类中可作为饱腹感信号,证实了先前在动物中报道的数据。