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- W2783758790 abstract "Endothelial cells (ECs) constitute the defensive barrier of vasculature, which maintains the vascular homeostasis. Mitochondrial oxidative stress (mitoOS) in ECs significantly affects the initiation and progression of vascular diseases. The higher serum thyroid stimulating hormone (TSH) level is being recognized as a nonconventional risk factor responsible for the increased risk of cardiovascular diseases in subclinical hypothyroidism (SCH). However, effects and underlying mechanisms of elevated TSH on ECs are still ambiguous. We sought to investigate whether cyclophilin D (CypD), emerging as a crucial mediator in mitoOS, regulates effects of TSH on ECs. SCH patients with TSH > = 10 mIU/L showed a positive correlation between serum TSH and endothelin-1 levels. When TSH levels declined to normal in these subjects after levothyroxine therapy, serum endothelin-1 levels were significantly reduced. Supplemented with exogenous thyroxine to keep normal thyroid hormones, thyroid-specific TSH receptor (TSHR)-knockout mice with injection of exogenous TSH exhibited elevated serum TSH levels, significant endothelial oxidative injuries and disturbed endothelium-dependent vasodilation. However, Tshr-/- mice resisted to TSH-impaired vasotonia. We further confirmed that elevated TSH triggered excessive mitochondrial permeability transition pore (mPTP) opening and mitochondrial oxidative damages in mouse aorta, as well as in cultured ECs. Genetic or pharmacological inhibition of CypD (the key regulator for mPTP opening) attenuated TSH-induced mitochondrial oxidative damages and further rescued endothelial functions. Finally, we confirmed that elevated TSH could activate CypD by enhancing CypD acetylation via inhibiting adenosine monophosphate-activated protein kinase/sirtuin-3 signaling pathway in ECs. These findings reveal that elevated TSH triggers mitochondrial perturbations in ECs and provide insights that blocking mitochondrial CypD enhances the defensive ability of ECs under TSH exposure." @default.
- W2783758790 created "2018-01-26" @default.
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- W2783758790 date "2018-05-01" @default.
- W2783758790 modified "2023-10-14" @default.
- W2783758790 title "Blocking mitochondrial cyclophilin D ameliorates TSH-impaired defensive barrier of artery" @default.
- W2783758790 cites W1509805561 @default.
- W2783758790 cites W1535057266 @default.
- W2783758790 cites W1864853792 @default.
- W2783758790 cites W1943357032 @default.
- W2783758790 cites W1966329382 @default.
- W2783758790 cites W1968257316 @default.
- W2783758790 cites W1969475086 @default.
- W2783758790 cites W1976599392 @default.
- W2783758790 cites W1983937216 @default.
- W2783758790 cites W1991436274 @default.
- W2783758790 cites W1993952575 @default.
- W2783758790 cites W1997684038 @default.
- W2783758790 cites W1998091253 @default.
- W2783758790 cites W2003468545 @default.
- W2783758790 cites W2006847107 @default.
- W2783758790 cites W2009568199 @default.
- W2783758790 cites W2011124873 @default.
- W2783758790 cites W2011963516 @default.
- W2783758790 cites W2012240256 @default.
- W2783758790 cites W2021460489 @default.
- W2783758790 cites W2029195231 @default.
- W2783758790 cites W2031297495 @default.
- W2783758790 cites W2033007699 @default.
- W2783758790 cites W2037586146 @default.
- W2783758790 cites W2043015190 @default.
- W2783758790 cites W2044080152 @default.
- W2783758790 cites W2045176648 @default.
- W2783758790 cites W2050958265 @default.
- W2783758790 cites W2051476652 @default.
- W2783758790 cites W2052737683 @default.
- W2783758790 cites W2057704034 @default.
- W2783758790 cites W2066200217 @default.
- W2783758790 cites W2074085679 @default.
- W2783758790 cites W2081641269 @default.
- W2783758790 cites W2082043462 @default.
- W2783758790 cites W2083791041 @default.
- W2783758790 cites W2091307458 @default.
- W2783758790 cites W2091574626 @default.
- W2783758790 cites W2094737751 @default.
- W2783758790 cites W2095756963 @default.
- W2783758790 cites W2097793695 @default.
- W2783758790 cites W2107886181 @default.
- W2783758790 cites W2116639256 @default.
- W2783758790 cites W2117977069 @default.
- W2783758790 cites W2120863778 @default.
- W2783758790 cites W2120963096 @default.
- W2783758790 cites W2128219988 @default.
- W2783758790 cites W2130266732 @default.
- W2783758790 cites W2130543706 @default.
- W2783758790 cites W2132416582 @default.
- W2783758790 cites W2134504365 @default.
- W2783758790 cites W2140388091 @default.
- W2783758790 cites W2140804599 @default.
- W2783758790 cites W2142296338 @default.
- W2783758790 cites W2149528066 @default.
- W2783758790 cites W2153298328 @default.
- W2783758790 cites W2160393206 @default.
- W2783758790 cites W2200357463 @default.
- W2783758790 cites W2203837377 @default.
- W2783758790 cites W2258231082 @default.
- W2783758790 cites W2340940178 @default.
- W2783758790 cites W2399674801 @default.
- W2783758790 cites W2530107877 @default.
- W2783758790 cites W2530627257 @default.
- W2783758790 cites W2541314532 @default.
- W2783758790 cites W2544091589 @default.
- W2783758790 cites W2548036931 @default.
- W2783758790 cites W2552967496 @default.
- W2783758790 cites W2554674760 @default.
- W2783758790 cites W2563785975 @default.
- W2783758790 cites W2577525077 @default.
- W2783758790 cites W2583713284 @default.
- W2783758790 cites W2592265119 @default.
- W2783758790 cites W2594740002 @default.
- W2783758790 cites W2615563405 @default.
- W2783758790 cites W2733051448 @default.
- W2783758790 cites W2735504036 @default.
- W2783758790 cites W2750846410 @default.
- W2783758790 cites W3015986900 @default.
- W2783758790 cites W4210343616 @default.