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过氧化物酶体增殖物激活受体(PPAR)介导的胆汁酸葡萄糖醛酸化:胆汁淤积性肝病治疗的靶点。

PPAR-Mediated Bile Acid Glucuronidation: Therapeutic Targets for the Treatment of Cholestatic Liver Diseases.

机构信息

Department of Biomedical and Pharmaceutical Sciences, College of Pharmacy, University of Rhode Island, Kingston, RI 02881, USA.

Section of Digestive Diseases, Yale School of Medicine, New Haven, CT 06510, USA.

出版信息

Cells. 2024 Aug 1;13(15):1296. doi: 10.3390/cells13151296.

Abstract

Cholestatic liver diseases, including primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC), result from an impairment of bile flow that leads to the hepatic retention of bile acids, causing liver injury. Until recently, the only approved treatments for PBC were ursodeoxycholic acid (UDCA) and obeticholic acid (OCA). While these therapies slow the progression of PBC in the early stage of the disease, approximately 40% of patients respond incompletely to UDCA, and advanced cases do not respond. UDCA does not improve survival in patients with PSC, and patients often have dose-limiting pruritus reactions to OCA. Left untreated, these diseases can progress to fibrosis and cirrhosis, resulting in liver failure and the need for transplantation. These shortcomings emphasize the urgent need for alternative treatment strategies. Recently, nuclear hormone receptors have been explored as pharmacological targets for adjunct therapy because they regulate enzymes involved in bile acid metabolism and detoxification. In particular, the peroxisome proliferator-activated receptor (PPAR) has emerged as a therapeutic target for patients with PBC or PSC who experience an incomplete response to UDCA. PPARα is predominantly expressed in the liver, and it plays an essential role in the regulation of cytochrome P450 (CYP) and uridine 5'-diphospho-glucuronosyltransferase (UGT) enzymes, both of which are critical enzyme families involved in the regulation of bile acid metabolism and glucuronidation, respectively. Importantly, PPARα agonists, e.g., fenofibrate, have shown therapeutic benefits in reducing elevated markers of cholestasis in patients with PBC and PSC, and elafibranor, the first PPAR (dual α, β/δ) agonist, has been FDA-approved for the second-line treatment of PBC. Additionally, newer PPAR agonists that target various PPAR isoforms (β/δ, γ) are under development as an adjunct therapy for PBC or PSC, although their impact on glucuronidation pathways are less characterized. This review will focus on PPAR-mediated bile acid glucuronidation as a therapeutic pathway to improve outcomes for patients with PBC and PSC.

摘要

胆汁淤积性肝病,包括原发性胆汁性胆管炎(PBC)和原发性硬化性胆管炎(PSC),是由于胆汁流动受损导致胆汁酸在肝脏中滞留,从而引起肝脏损伤。直到最近,PBC 的唯一批准治疗方法是熊去氧胆酸(UDCA)和奥贝胆酸(OCA)。虽然这些疗法在疾病早期阶段减缓了 PBC 的进展,但大约 40%的患者对 UDCA 反应不完全,而晚期病例则没有反应。UDCA 不能改善 PSC 患者的生存率,而且患者经常对 OCA 产生剂量限制的瘙痒反应。如果不进行治疗,这些疾病会进展为纤维化和肝硬化,导致肝衰竭和需要进行移植。这些缺点强调了急需替代治疗策略。最近,核激素受体已被探索为辅助治疗的药理学靶点,因为它们调节参与胆汁酸代谢和解毒的酶。特别是,过氧化物酶体增殖物激活受体(PPAR)已成为对 UDCA 反应不完全的 PBC 或 PSC 患者的治疗靶点。PPARα 主要在肝脏中表达,在调节细胞色素 P450(CYP)和尿苷 5'-二磷酸葡萄糖醛酸转移酶(UGT)酶方面发挥着至关重要的作用,这两种酶都是分别参与胆汁酸代谢和葡萄糖醛酸化调节的关键酶家族。重要的是,PPARα 激动剂,如非诺贝特,已显示出在降低 PBC 和 PSC 患者胆汁淤积升高标志物方面的治疗益处,而作为首个 PPAR(双重α、β/δ)激动剂的 Elafibranor 已被 FDA 批准用于 PBC 的二线治疗。此外,正在开发针对各种 PPAR 同工型(β/δ、γ)的新型 PPAR 激动剂,作为 PBC 或 PSC 的辅助治疗方法,尽管它们对葡萄糖醛酸化途径的影响特征较少。本综述将重点介绍 PPAR 介导的胆汁酸葡萄糖醛酸化作为改善 PBC 和 PSC 患者结局的治疗途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b58/11312002/25c6265f6587/cells-13-01296-g001.jpg

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