Duplanty Anthony A, Siggins Robert W, Allerton Timothy, Simon Liz, Molina Patricia E
Department of Physiology, Comprehensive Alcohol Research Center, Alcohol and Drug Abuse Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
Physiol Rep. 2018 Mar;6(5). doi: 10.14814/phy2.13625.
Work from our group demonstrated that chronic binge alcohol (CBA)-induces mitochondrial gene dysregulation at end-stage disease of simian immunodeficiency virus (SIV) infection in antiretroviral therapy (ART) naïve rhesus macaques. Alterations in gene expression can disrupt mitochondrial homeostasis and in turn contribute to the risk of metabolic comorbidities characterized by loss of skeletal muscle (SKM) functional mass that are associated with CBA, human immunodeficiency virus (HIV) infection, and prolonged ART. The aim of this study was to examine the interaction of CBA and ART on SKM fiber oxidative capacity and myoblast mitochondrial respiration in asymptomatic SIV-infected macaques. SKM biopsies were obtained and myoblasts isolated at baseline and 11 months post-SIV infection from CBA/SIV/ART+ and from sucrose (SUC)-treated SIV-infected (SUC/SIV/ART+) macaques. CBA and ART decreased succinate dehydrogenase (SDH) activity in type 1 and type 2b fibers as determined by immunohistochemistry. Myoblasts isolated from CBA/SIV/ART+ macaques showed decreased maximal oxygen consumption rate (OCR) compared to myoblasts from control macaques. Maximal OCR was significantly increased in control myoblasts following incubation with formoterol, a beta adrenergic agonist, and this was associated with increased PGC-1α expression and mtDNA quantity. Additionally, formoterol treatment of myoblasts isolated from CBA/SIV/ART+ macaques partially restored maximal OCR to levels not significantly different from control. These results show that CBA in combination with ART impairs myoblast mitochondrial homeostasis in SIV-infected macaques. Moreover, our findings suggest that adrenergic agonists can potentially ameliorate mitochondrial dysfunction. Future studies will elucidate whether physical exercise in HIV patients with alcohol use disorder can improve mitochondrial health.
我们团队的研究表明,在未接受抗逆转录病毒治疗(ART)的感染猿猴免疫缺陷病毒(SIV)的恒河猴终末期疾病中,慢性暴饮酒精(CBA)会导致线粒体基因失调。基因表达的改变会破坏线粒体稳态,进而增加代谢合并症的风险,这些合并症的特征是骨骼肌(SKM)功能质量丧失,与CBA、人类免疫缺陷病毒(HIV)感染及长期ART治疗有关。本研究的目的是探讨CBA和ART对无症状SIV感染猕猴的SKM纤维氧化能力和成肌细胞线粒体呼吸的相互作用。在基线以及SIV感染后11个月,从接受CBA/SIV/ART+治疗的猕猴和接受蔗糖(SUC)治疗的SIV感染猕猴(SUC/SIV/ART+)获取SKM活检样本并分离成肌细胞。通过免疫组织化学测定,CBA和ART降低了1型和2b型纤维中的琥珀酸脱氢酶(SDH)活性。与对照猕猴的成肌细胞相比,从CBA/SIV/ART+猕猴分离出的成肌细胞显示最大耗氧率(OCR)降低。在用β肾上腺素能激动剂福莫特罗孵育后,对照成肌细胞中的最大OCR显著增加,这与PGC-1α表达增加和线粒体DNA数量增加有关。此外,用福莫特罗处理从CBA/SIV/ART+猕猴分离出的成肌细胞可将最大OCR部分恢复至与对照无显著差异的水平。这些结果表明,CBA与ART联合使用会损害SIV感染猕猴的成肌细胞线粒体稳态。此外,我们的研究结果表明,肾上腺素能激动剂可能会改善线粒体功能障碍。未来的研究将阐明,患有酒精使用障碍的HIV患者进行体育锻炼是否能改善线粒体健康。