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A型胆囊收缩素受体介导胆囊收缩素-8对9至12日龄幼鼠食物摄入和活动的抑制作用。

Type-A CCK receptors mediate the inhibition of food intake and activity by CCK-8 in 9- to 12-day-old rat pups.

作者信息

Smith G P, Tyrka A, Gibbs J

机构信息

Department of Psychiatry, Cornell University Medical College, White Plains, NY.

出版信息

Pharmacol Biochem Behav. 1991 Jan;38(1):207-10. doi: 10.1016/0091-3057(91)90612-6.

DOI:10.1016/0091-3057(91)90612-6
PMID:2017446
Abstract

To determine the type of cholecystokinin (CCK) receptor that mediates the inhibitory effects of peripherally administered CCK-8 on food intake and activity in 9- to 12-day-old rat pups, we gave injections of a type-A CCK receptor antagonist, MK-329, or of the type-B CCK receptor antagonist, L-365,260, prior to CCK-8 (IP). MK-329 reversed the inhibitory effects of CCK-8, but L-365,260 did not. This demonstrates that the inhibitory effects of CCK-8 (IP) are mediated by type-A, but not type-B, CCK receptors in pups of this age.

摘要

为了确定介导外周给予的胆囊收缩素八肽(CCK-8)对9至12日龄幼鼠食物摄取和活动的抑制作用的胆囊收缩素(CCK)受体类型,我们在腹腔注射CCK-8之前,注射了A型CCK受体拮抗剂MK-329或B型CCK受体拮抗剂L-365,260。MK-329逆转了CCK-8的抑制作用,但L-365,260没有。这表明,在此年龄的幼鼠中,腹腔注射CCK-8的抑制作用是由A型而非B型CCK受体介导的。

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1
Type-A CCK receptors mediate the inhibition of food intake and activity by CCK-8 in 9- to 12-day-old rat pups.A型胆囊收缩素受体介导胆囊收缩素-8对9至12日龄幼鼠食物摄入和活动的抑制作用。
Pharmacol Biochem Behav. 1991 Jan;38(1):207-10. doi: 10.1016/0091-3057(91)90612-6.
2
Postponement of satiety by blockade of brain cholecystokinin (CCK-B) receptors.通过阻断脑胆囊收缩素(CCK - B)受体来延迟饱腹感。
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Effects of CCK antagonists on CCK-induced suppression of locomotor activity in mice.胆囊收缩素拮抗剂对胆囊收缩素诱导的小鼠运动活动抑制的影响。
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Endogenous cholecystokinin reduces feeding in young rats.内源性胆囊收缩素可减少幼鼠的进食量。
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Age-dependent effects of CCK and devazepide in male and female rats.胆囊收缩素(CCK)和地伐西匹对雄性和雌性大鼠的年龄依赖性影响。
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Centrally administered cholecystokinin suppresses feeding through a peripheral-type receptor mechanism.中枢给予的胆囊收缩素通过外周型受体机制抑制进食。
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Subtype-selective cholecystokinin receptor antagonists block cholecystokinin modulation of dopamine-mediated behaviors in the rat mesolimbic pathway.亚型选择性胆囊收缩素受体拮抗剂可阻断胆囊收缩素对大鼠中脑边缘通路中多巴胺介导行为的调节作用。
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The CCK-A receptor antagonist devazepide but not the CCK-B receptor antagonist L-365,260 reverses the effects of chronic clozapine and haloperidol on midbrain dopamine neurons.胆囊收缩素 A 型受体拮抗剂地伐西匹可逆转慢性氯氮平和氟哌啶醇对中脑多巴胺能神经元的作用,而胆囊收缩素 B 型受体拮抗剂 L-365,260 则不能。
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Changes in motor activity and forebrain [propionyl-3H]propionylated-CCK-8 binding in mice after repeated administration of drugs affecting cholecystokinin receptors.反复给予影响胆囊收缩素受体的药物后小鼠运动活性及前脑[丙酰基-³H]丙酰化胆囊收缩素-8结合的变化
Eur J Pharmacol. 1991 Sep 24;202(3):385-90. doi: 10.1016/0014-2999(91)90283-v.
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Loxiglumide, L-364,718 and L-365,260 prevent the inhibition of spontaneous acetylcholine release from the frontal cerebral cortex of freely moving rat peripherally administered with cholecystokinin-8S.洛西格列胺、L-364,718和L-365,260可防止外周给予八肽胆囊收缩素的自由活动大鼠额叶皮质中自发性乙酰胆碱释放受到抑制。
Jpn J Pharmacol. 1995 May;68(1):129-32. doi: 10.1254/jjp.68.129.

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