In-vivo Modulation of Gastrointestinal Motility by Cannabinoid Drugs

A. Izzo, Domenico Addeo, M. Amato, F. Borrelli, R. Capasso, G. Carlo, Emilia Nocerino, N. Mascolo, L. Pinto, F. Capasso
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引用次数: 2

Abstract

Cannabinoid CB1 receptors have been detected in several peripheral neurons, including those of the myenteric plexus. Activation of myenteric (prejunctional located) cannabinoid CB1 receptors decreased intestinal motility induced by electrical stimulation in the isolated guinea-pig and human ileum. In-vivo studies have shown that cannabinoid receptor agonists decreased gastrointestinal motility through activation of cannabinoid CB1 receptors, while SR141716A, a cannabinoid CB1-receptor antagonist, increased intestinal motility. Both central and peripheral cannabinoid CB1 receptors could modulate upper gastrointestinal, but the effect of systemic (intraperitoneally injected) cannabinoid drugs was mediated by peripheral receptors. In addition, the potency of cannabinoid receptor agonists was increased during inflammatory diarrhoea.
大麻素类药物对胃肠运动的体内调节
大麻素CB1受体在一些外周神经元中被检测到,包括那些肌肠丛。在离体豚鼠和人回肠中,肌际(交界前位置)大麻素CB1受体的激活降低了电刺激诱导的肠道运动。体内研究表明,大麻素受体激动剂通过激活大麻素CB1受体降低胃肠蠕动,而大麻素CB1受体拮抗剂SR141716A增加肠道蠕动。中枢和外周大麻素CB1受体都能调节上消化道,但全身(腹腔注射)大麻素药物的作用是由外周受体介导的。此外,大麻素受体激动剂的效力在炎症性腹泻期间增加。
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