Krause B R, Sliskovic D R, Anderson M, Homan R
Department of Vascular & Cardiac Diseases, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor, Michigan 48105, USA.
Lipids. 1998 May;33(5):489-98. doi: 10.1007/s11745-998-0232-8.
WAY-121,898 is an inhibitor of pancreatic cholesteryl ester hydrolase (pCEH). After confirming its in vitro potency and relative lack of a major effect on acyl-CoA:cholesterol acyltransferase (ACAT), it was found that this compound lowers plasma cholesterol in cholesterol-fed, but not chow-fed, rats. Measures of liver cholesteryl ester content and the direct determination of cholesterol absorption (lymph-fistula model) show that inhibition of cholesterol absorption is at least one mechanism for the observed cholesterol lowering. However, WAY-121,898 was also active when administered parenterally to cholesterol-fed rats, and in cholesterol-fed hamsters cholesterol-lowering occurred with oral dosing despite no change in cholesterol absorption, suggesting other modes of action possibly relating to inhibition of liver CEH. Combination treatment in cholesterol-fed rats with the ACAT inhibitor CI-976 resulted in a greater-than-additive reduction in plasma cholesterol, implying that both pCEH and ACAT may play a role in cholesterol absorption in this species. In rabbits, WAY-121,898 prevented the rise in plasma cholesterol due to the feeding of cholesteryl ester but not in rabbits fed (free) cholesterol. In guinea pigs, the compound induced an increase in adrenal cholesteryl ester mass. Taken together, the overall profile in these animal models suggests that WAY-121,898 inhibits more than just the intestinal (lumenal) pCEH, and that the role of this enzyme in cholesterol metabolism may be different within and across species, the former depending upon the dietary cholesterol load.
WAY-121,898是一种胰腺胆固醇酯水解酶(pCEH)抑制剂。在确认其体外效力以及对酰基辅酶A:胆固醇酰基转移酶(ACAT)相对缺乏主要影响后,发现该化合物可降低喂食胆固醇而非普通饲料的大鼠的血浆胆固醇。肝脏胆固醇酯含量的测定以及胆固醇吸收的直接测定(淋巴瘘模型)表明,抑制胆固醇吸收至少是观察到的胆固醇降低的一种机制。然而,当对喂食胆固醇的大鼠进行肠胃外给药时,WAY-121,898也具有活性,并且在喂食胆固醇的仓鼠中,口服给药会降低胆固醇,尽管胆固醇吸收没有变化,这表明可能存在与抑制肝脏CEH相关的其他作用方式。在喂食胆固醇的大鼠中,将WAY-121,898与ACAT抑制剂CI-976联合治疗导致血浆胆固醇的降低幅度大于相加效应,这意味着pCEH和ACAT在该物种的胆固醇吸收中可能都起作用。在兔子中,WAY-121,898可防止因喂食胆固醇酯而导致的血浆胆固醇升高,但对喂食(游离)胆固醇的兔子则无效。在豚鼠中,该化合物可导致肾上腺胆固醇酯质量增加。综上所述,这些动物模型中的总体情况表明,WAY-121,898不仅抑制肠道(肠腔)pCEH,而且该酶在胆固醇代谢中的作用在物种内部和物种之间可能有所不同,前者取决于饮食中的胆固醇负荷。