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• W2953233488 abstract "When it comes to obesity, men exhibit a higher incidence of metabolic syndrome than women in early adult life, but this sex advantage wanes in postmenopausal women. A key diagnostic of the metabolic syndrome is insulin resistance in both peripheral tissues and brain, especially in the hypothalamus. Since the anorexigenic hormone 17β-estradiol (E₂) regulates food intake in part by inhibiting the excitability of the hypothalamic neuropeptide Y/agouti-related peptide (NPY/AgRP) neurons, we hypothesized that E₂ would protect against insulin resistance in NPY/AgRP neurons with diet-induced obesity (DIO). Therefore, we did whole-cell recordings and single cell quantitative polymerase chain reaction in arcuate NPY^GFP neurons from both female and male mice to test the efficacy of insulin with DIO. The resting membrane potential and input resistance of NPY/AgRP neurons were significantly increased in DIO versus control-diet fed males. Most notably, the efficacy of insulin to activate K_ATP channels in NPY/AgRP neurons was significantly attenuated, although the K_ATP channel opener diazoxide was fully effective in NPY/AgRP neurons from DIO males, indicating that the K_ATP channels were expressed and functional. In contrast, insulin was fully efficacious to activate K_ATP channels in DIO females, and the response was reversed by the K_ATP channel blocker tolbutamide. However, the ability of insulin to activate K_ATP channels was abrogated with ovariectomy but fully restored with E₂ replacement. Insulin resistance in obese males was likely mediated by an increase in suppressor of cytokine signaling-3 (SOCS-3), protein tyrosine phosphatase B (PTP1B) and T-cell protein tyrosine phosphatase (TCPTP) activity, since the expression of all 3 mRNAs were upregulated in the obese males but not in females. As proof of principle, pre-incubation of hypothalamic slices from DIO males with the PTP1B/TCPTP inhibitor CX08005 completely rescued the effects of insulin. Therefore, E₂ protects NPY/AgRP neurons in females against insulin resistance through, at least in part, attenuating phosphatase activity. The neuroprotective effects of E₂ may explain sex differences in the expression of metabolic syndrome that disappears with the loss of E₂ in aging." @default.
• W2953233488 created "2019-06-27" @default.
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• W2953233488 date "2019-06-19" @default.
• W2953233488 modified "2023-10-18" @default.
• W2953233488 title "Estradiol Protects Neuropeptide Y/Agouti-Related Peptide Neurons against Insulin Resistance in Females" @default.
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• W2953233488 doi "https://doi.org/10.1159/000501560" @default.
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