Johnson Timothy E, Zhang Xiaohua, Shi Shu, Umbenhauer Diane R
Department of Safety Assessment, Merck Research Laboratories, WP45-319, Merck Research Laboratories, West Point, PA 19486, USA.
Toxicol Appl Pharmacol. 2005 Nov 1;208(3):210-21. doi: 10.1016/j.taap.2005.03.004.
Statins and fibrates (weak PPARalpha agonists) are prescribed for the treatment of lipid disorders. Both drugs cause myopathy, but with a low incidence, 0.1-0.5%. However, combined statin and fibrate therapy can enhance myopathy risk. We tested the myotoxic potential of PPAR subtype selective agonists alone and in combination with statins in a differentiated rat myotube model. A pharmacologically potent experimental PPARalpha agonist, Compound A, induced myotoxicity as assessed by TUNEL staining at a minimum concentration of 1 nM, while other weaker PPARalpha compounds, for example, WY-14643, Gemfibrozil and Bezafibrate increased the percentage of TUNEL-positive nuclei at micromolar concentrations. In contrast, the PPARgamma agonist Rosiglitazone caused little or no cell death at up to 10 muM and the PPARdelta ligand GW-501516 exhibited comparatively less myotoxicity than that seen with Compound A. An experimental statin (Compound B) and Atorvastatin also increased the percentage of TUNEL-positive nuclei and co-treatment with WY-14643, Gemfibrozil or Bezafibrate had less than a full additive effect on statin-induced cell killing. The mechanism of PPARalpha agonist-induced cell death was different from that of statins. Unlike statins, Compound A and WY-14643 did not activate caspase 3/7. In addition, mevalonate and geranylgeraniol reversed the toxicity caused by statins, but did not prevent the cell killing induced by WY-14643. Furthermore, unlike statins, Compound A did not inhibit the isoprenylation of rab4 or rap1a. Interestingly, Compound A and Compound B had differential effects on ATP levels. Taken together, these observations support the hypothesis that in rat myotube cultures, PPARalpha agonism mediates in part the toxicity response to PPARalpha compounds. Furthermore, PPARalpha agonists and statins cause myotoxicity through distinct and independent pathways.
他汀类药物和贝特类药物(弱PPARα激动剂)被用于治疗脂质紊乱。这两种药物都会引起肌病,但发病率较低,为0.1 - 0.5%。然而,他汀类药物和贝特类药物联合治疗会增加肌病风险。我们在分化的大鼠肌管模型中测试了PPAR亚型选择性激动剂单独以及与他汀类药物联合使用时的肌毒性潜力。一种具有药理活性的实验性PPARα激动剂化合物A,在最低浓度为1 nM时通过TUNEL染色评估可诱导肌毒性,而其他较弱的PPARα化合物,例如WY - 14643、吉非贝齐和苯扎贝特,在微摩尔浓度下会增加TUNEL阳性细胞核的百分比。相比之下,PPARγ激动剂罗格列酮在高达10 μM时几乎不引起或不引起细胞死亡,并且PPARδ配体GW - 501516表现出比化合物A相对较小的肌毒性。一种实验性他汀类药物(化合物B)和阿托伐他汀也会增加TUNEL阳性细胞核的百分比,并且与WY - 14643、吉非贝齐或苯扎贝特联合治疗对他汀类药物诱导的细胞杀伤作用小于完全相加效应。PPARα激动剂诱导细胞死亡的机制与他汀类药物不同。与他汀类药物不同,化合物A和WY - 14643不会激活半胱天冬酶3/7。此外,甲羟戊酸和香叶基香叶醇可逆转他汀类药物引起的毒性,但不能预防WY - 14643诱导的细胞杀伤。此外,与他汀类药物不同,化合物A不会抑制rab4或rap1a的异戊二烯化。有趣的是,化合物A和化合物B对ATP水平有不同的影响。综上所述,这些观察结果支持以下假设:在大鼠肌管培养中,PPARα激动作用部分介导了对PPARα化合物的毒性反应。此外,PPARα激动剂和他汀类药物通过不同且独立的途径引起肌毒性。