The pruritus of cholestasis: From bile acids to opiate agonists: Relevant after all these years

被引:34
作者
Bergasa, Nora V. [1 ,2 ]
机构
[1] PAGNY, H H, New York, NY USA
[2] New York Med Coll, Valhalla, NY 10595 USA
关键词
PRIMARY BILIARY-CIRRHOSIS; ORAL NALTREXONE TREATMENT; PLACEBO-CONTROLLED TRIAL; OPIOID RECEPTOR AGONIST; HEPATIC MET-ENKEPHALIN; BLOOD-BRAIN-BARRIER; LIVER-DISEASE; DOUBLE-BLIND; RAT MODEL; NALOXONE INFUSIONS;
D O I
10.1016/j.mehy.2017.11.002
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The pruritus of cholestasis is a maddening complication of liver disease. Increased opioidergic tone contributes to the pruritus of cholestasis, as evidenced by the amelioration of the symptom by opiate antagonists. Obeticholic acid, an agonist of the farnesoid receptor, has been approved for the treatment of primary biliary cholangitis, a disease characterized by cholestasis; this drug is associated with pruritus, the cause of which is unknown. In animal models, bile acids, which accumulate in the body as a result of cholestasis, have been reported to cause scratching behavior mediated by the TGR5 receptor, in an opioid-dependent manner, in laboratory animals. As obeticholic acid also binds to TGR5, the pruritus caused by this drug is likely to be mediated by the opioid system. Lisophosphatidic acid, which has been reported to be increased in patients with cholestasis and pruritus, has been described to cause scratching behavior that is prevented by an opiate antagonist in laboratory animals, suggesting an opioid-receptor mediated mechanism of scratching. In summary, evidence continues to support a role of the endogenous opioid system in the pathogenesis of the pruritus of cholestasis
引用
收藏
页码:86 / 89
页数:4
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