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• W2088392207 abstract "Atherosclerosis is one of the major complications of diabetes, which may result from insulin resistance via mitochondrial dysfunction. Although a strong association between insulin resistance and cardiovascular disease has been suggested, it is not clear yet whether stress-inducing factors damage mitochondria and insulin signaling pathway in cardiovascular tissues. We investigated whether stress-induced mitochondrial dysfunction might alter the insulin/Akt signaling pathway in A10 rat vascular smooth muscle cells (VSMC). The treatment of oxidized low density lipoprotein (oxLDL) decreased ATP contents, mitochondrial respiration activity, mRNA expressions of OXPHOS subunits and IRS-1/2 and insulin-mediated phosphorylations of Akt and AMP-activated protein kinase (AMPK). Similarly, dideoxycytidine (ddC), the mtDNA replication inhibitor, or rotenone, OXPHOS complex I inhibitor, inhibited the insulin-mediated pAkt while increased pAMPK regardless of insulin. Reciprocally, an inhibitor of Akt, triciribine (TCN), decreased cellular ATP contents. Overexpression of Akt dominant positive reversed the oxLDL- or ddC-mediated ATP decrease but AMPK activator did not. Akt activation also normalized the aberrant VSMC migration induced by ddC. Defective insulin signaling and mitochondrial function may collectively contribute to developing cardiovascular disease. Akt may be a possible therapeutic target for treating insulin resistance-associated atherosclerosis." @default.
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• W2088392207 date "2010-03-01" @default.
• W2088392207 modified "2023-10-16" @default.
• W2088392207 title "Mitochondrial dysfunction enhances the migration of vascular smooth muscles cells via suppression of Akt phosphorylation" @default.
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• W2088392207 doi "https://doi.org/10.1016/j.bbagen.2009.09.005" @default.
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