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苯二氮䓬类药物对蛙皮素在小鼠食物摄入量方面的拮抗作用。

Caerulein antagonism by benzodiazepines in the food intake in mice.

作者信息

Kubota K, Sugaya K, Matsuda I, Matsuoka Y, Itonaga M

出版信息

Jpn J Pharmacol. 1985 Sep;39(1):120-2. doi: 10.1254/jjp.39.120.

DOI:10.1254/jjp.39.120
PMID:2866264
Abstract

Intracisternal administration of caerulein inhibited the food intake in mice, but the caerulein action was antagonized by benzodiazepines such as chlordiazepoxide, diazepam and flurazepam which were administered intraperitoneally in low doses (0.2 to 2 mg/kg). The antagonism mechanism between caerulein and benzodiazepines remains unclear, but the characteristics of the antagonism were similar to those which had been observed with cholecystokinin and benzodiazepines.

摘要

向脑池内注射蛙皮素可抑制小鼠的食物摄取,但蛙皮素的作用可被腹腔注射低剂量(0.2至2毫克/千克)的苯二氮卓类药物如氯氮卓、地西泮和氟西泮所拮抗。蛙皮素与苯二氮卓类药物之间的拮抗机制尚不清楚,但这种拮抗作用的特征与胆囊收缩素和苯二氮卓类药物之间所观察到的相似。

相似文献

1
Caerulein antagonism by benzodiazepines in the food intake in mice.苯二氮䓬类药物对蛙皮素在小鼠食物摄入量方面的拮抗作用。
Jpn J Pharmacol. 1985 Sep;39(1):120-2. doi: 10.1254/jjp.39.120.
2
Cholecystokinin antagonism by benzodiazepines in the food intake in mice.苯二氮䓬类药物对小鼠食物摄入量的胆囊收缩素拮抗作用。
Physiol Behav. 1986 Jan;36(1):175-8. doi: 10.1016/0031-9384(86)90092-2.
3
Reversal of antinociceptive effect of caerulein by benzodiazepine.苯二氮䓬类药物对蛙皮素抗伤害感受作用的逆转
J Pharmacobiodyn. 1986 Apr;9(4):428-31. doi: 10.1248/bpb1978.9.428.
4
Reversal of antinociceptive effect of cholecystokinin by benzodiazepines and a benzodiazepine antagonist, Ro 15-1788.
Jpn J Pharmacol. 1985 Jan;37(1):101-5. doi: 10.1254/jjp.37.101.
5
Antagonism of central and peripheral anorectic effects of caerulein by L-364,718.L-364,718对蛙皮素中枢和外周厌食作用的拮抗作用。
Eur J Pharmacol. 1989 Feb 28;161(2-3):255-8. doi: 10.1016/0014-2999(89)90855-8.
6
Inhibition of hypothermic effect of cholecystokinin by benzodiazepines and a benzodiazepine antagonist, Ro 15-1788, in mice.
Jpn J Pharmacol. 1985 Oct;39(2):277-80. doi: 10.1254/jjp.39.277.
7
Cholecystokinin antagonism by benzodiazepines in the contractile response of the isolated guinea-pig gallbladder.
Eur J Pharmacol. 1985 Apr 2;110(2):225-31. doi: 10.1016/0014-2999(85)90215-8.
8
Possible involvement of the CCK receptor in the benzodiazepine antagonism to CCK in the mouse brain.胆囊收缩素受体可能参与苯二氮䓬对小鼠大脑中胆囊收缩素的拮抗作用。
Jpn J Pharmacol. 1987 Jan;43(1):67-71. doi: 10.1254/jjp.43.67.
9
Reduction of food intake by central administration of cholecystokinin octapeptide in the rat is dependent upon inhibition of brain peptidases.通过向大鼠中枢注射八肽胆囊收缩素减少食物摄入量取决于对脑肽酶的抑制作用。
Br J Pharmacol. 1989 Jan;96(1):236-42. doi: 10.1111/j.1476-5381.1989.tb11805.x.
10
Caerulein and cholecystokinin octapeptide (CCK-8): sedative and anticonvulsive effects in mice unaffected by the benzodiazepine antagonist Ro 15-1788.蛙皮素和胆囊收缩素八肽(CCK - 8):对小鼠的镇静和抗惊厥作用不受苯二氮䓬拮抗剂Ro 15 - 1788的影响。
Neurosci Lett. 1982 Mar 5;28(3):287-90. doi: 10.1016/0304-3940(82)90072-6.

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Anxiogenic-like action of caerulein, a CCK-8 receptor agonist, in the mouse: influence of acute and subchronic diazepam treatment.
Naunyn Schmiedebergs Arch Pharmacol. 1990 Jan-Feb;341(1-2):62-7. doi: 10.1007/BF00195059.