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β-酪蛋白吗啡对豚鼠结肠肠道推进的影响。

Effect of beta-casomorphins on intestinal propulsion in the guinea-pig colon.

作者信息

De Ponti F, Marcoli M, Lecchini S, Manzo L, Frigo G M, Crema A

机构信息

Department of Internal Medicine and Therapeutics, University of Pavia, Italy.

出版信息

J Pharm Pharmacol. 1989 May;41(5):302-5. doi: 10.1111/j.2042-7158.1989.tb06461.x.

Abstract

beta-Casomorphins are a family of opioid peptides originally isolated from beta-casein. In view of a possible physiological significance of these milk-derived compounds, the effects of bovine beta-casomorphin-5 (beta-CM-5), beta-casomorphin-4 (beta-CM-4) and D-Ala2-beta-casomorphin-4-NH2 (D-Ala2-beta-CM-4-NH2) have been investigated on the peristaltic reflex in the guinea-pig isolated colon and compared with morphine. beta-CM-5 and D-Ala2-beta-CM-4-NH2 each dose-dependently inhibited the velocity of propulsion of an intraluminal bolus; beta-CM-4 was ineffective. IC50 values were 0.30, 5.21 and 0.29 microM for morphine, beta-CM-5 and D-Ala2-beta-CM-4-NH2, respectively. The potency ratios vs morphine were 0.06 and 0.96 for beta-CM-5 and D-Ala2-beta-CM-4-NH2, respectively. Blockade of the peristaltic reflex by beta-CM-5 or D-Ala2-beta-CM-4-NH2 was reversed by the opioid antagonist naloxone. D-Ala2-beta-CM-4-NH2 also dose-dependently inhibited resting acetylcholine output (IC50 = 5.69 microM; potency ratio vs morphine: 0.63). In conclusion, certain beta-casomorphins inhibit intestinal propulsion and cholinergic neurotransmission in the guinea-pig colon, probably by acting at opioid receptors.

摘要

β-酪蛋白吗啡是一类最初从β-酪蛋白中分离出来的阿片肽。鉴于这些源自牛奶的化合物可能具有的生理意义,研究了牛β-酪蛋白吗啡-5(β-CM-5)、β-酪蛋白吗啡-4(β-CM-4)和D-丙氨酸2-β-酪蛋白吗啡-4-氨基(D-Ala2-β-CM-4-NH2)对豚鼠离体结肠蠕动反射的影响,并与吗啡进行了比较。β-CM-5和D-Ala2-β-CM-4-NH2均剂量依赖性地抑制肠腔内团块的推进速度;β-CM-4无效。吗啡、β-CM-5和D-Ala2-β-CM-4-NH2的半数抑制浓度(IC50)值分别为0.30、5.21和0.29微摩尔。β-CM-5和D-Ala2-β-CM-4-NH2与吗啡相比的效价比分别为0.06和0.96。β-CM-5或D-Ala2-β-CM-4-NH2对蠕动反射的阻断作用可被阿片拮抗剂纳洛酮逆转。D-Ala2-β-CM-4-NH2也剂量依赖性地抑制静息乙酰胆碱的释放(IC50 = 5.69微摩尔;与吗啡相比的效价比:0.63)。总之,某些β-酪蛋白吗啡可能通过作用于阿片受体来抑制豚鼠结肠的肠推进和胆碱能神经传递。

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