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首页> 外文期刊>Molecular and Cellular Endocrinology >Reverse T-3 interacts with alpha vr beta 3 integrin receptor and restores enzyme activities in the hippocampus of hypothyroid developing rats: Insight on signaling mechanisms
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Reverse T-3 interacts with alpha vr beta 3 integrin receptor and restores enzyme activities in the hippocampus of hypothyroid developing rats: Insight on signaling mechanisms

机译:反向T-3与αVRβ3整联蛋白受体相互作用,并在甲状腺功能率发育大鼠的海马中恢复酶活性:关于信号机制的洞察力

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In the present study we provide evidence that 3,3',5'-triiodothyronine (reverse T-3, rT(3)) restores neurochemical parameters induced by congenital hypothyroidism in rat hippocampus. Congenital hypothyroidism was induced by adding 0.05% propylthiouracil in the drinking water from gestation day 8 and continually up to lactation day 15. In the in vivo rT(3) exposure, hypothyroid 12-day old pups were daily injected with rT(3) (50 ng/kg body weight) or saline until day 14. In the ex vivo rT(3) treatment, hippocampal slices from 15-day-old hypothyroid pups were incubated for 30 min with or without rT(3) (1 nM). We found that ex vivo and/or in vivo exposure to rT(3) failed in restoring the decreased I t-glutamate uptake; however, restored the phosphorylation of glial fibrillary acidic protein (GFAP), Ca-45(2-) influx, aspartate transaminase (AST), glutamine synthetase (GS) and gamma-glutamate transferase (GGT) activities, as well as glutathione (GSH) levels in hypothyroid hippocampus. In addition, rT(3) improved C-14-2-deoxy-D-glucose uptake and lactate dehydrogenase (LDH) activity. Receptor agonists/antagonists (RGD peptide and AP-5), kinase inhibitors of p38MAPK, ERK1/2, CaMKII, PKA (SB239063, PD98059, KN93 and H89, respectively), L-type voltage-dependent calcium channel blocker (nifedipine) and intracellular calcium chelator (BAPTA-AM) were used to determine the mechanisms of the nongenomic rT(3) action on GGT activity. Using molecular docking analysis, we found rT(3) interaction with alpha vr beta 3 integrin receptors, nongenomically activating signaling pathways (PKA, CaMKII, p38MAPK) that restored GGT activity. We provide evidence that rT(3) is an active TH metabolite and our results represent an important contribution to elucidate the nonclassical mechanism of action of this metabolite in hypothyroidism. (C) 2017 Elsevier B.V. All rights reserved.
机译:在本研究中,我们提供了3,3',5'-三碘甲酚(反向T-3,RT(3))恢复先天性甲状腺功能亢进症诱导的神经化学参数在大鼠海马中恢复。通过在妊娠第8天中加入饮用水中的0.05%丙基硫胺诱导先天性甲状腺功能亢进,并持续到第15天。在体内RT(3)暴露中,每天注射甲状腺炎症12日龄幼崽(3)(3)(3)( 50 ng / kg体重)或盐水直到14天。在前体内RT(3)处理中,将15天左右甲状腺幼虫幼仔的海马切片有或没有RT(3)(1nM)孵育30分钟。我们发现离体和/或体内暴露于室温(3)未能恢复降低的I-谷氨酸摄取;然而,恢复胶质纤维酸性蛋白(GFAP),Ca-45(2-)流入,天冬氨酸转氨酶(AST),谷氨酰胺合成酶(GS)和γ-谷氨酸转移酶(GGT)活性以及谷胱甘肽(GSH)的磷酸化合物(GSH )甲状管状海马水平。此外,RT(3)改善C-14-2-脱氧-D-葡萄糖摄取和乳酸脱氢酶(LDH)活性。受体激动剂/拮抗剂(RGD肽和AP-5),P38MAPK,ERK1 / 2,CAMKII,PKA(SB239063,PD98059,KN93和H89分别),L型电压依赖性钙通道阻滞剂(NiFemipine)和抗激酶抑制剂细胞内钙螯合剂(Bapta-AM)用于确定Nongenomic Rt(3)对GGT活性作用的机制。使用分子对接分析,我们发现RT(3)与αVRβ3整联蛋白受体的相互作用,Nongenomics激活信号通路(PKA,Camkii,P38mapk)恢复GGT活性。我们提供RT(3)的证据是一种活跃的代谢物,我们的结果代表了阐明甲状腺功能亢进中该代谢物的非生物作用机制的重要贡献。 (c)2017 Elsevier B.v.保留所有权利。

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