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Perspective of future drugs targeting sterile 20/SPS1-related proline/alanine-rich kinase for blood pressure control
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作者 Gen-Min Lin Pang-Yen Liu +2 位作者 Ching-Fen Wu Wen-Been Wang Chih-Lu Han 《World Journal of Cardiology》 CAS 2015年第6期306-310,共5页
According to a genome-wide association study,intronic SNPs within the human sterile 20/SPS1-related proline/alanine-rich kinase(SPAK) gene was linked to 20% of the general population and may be associated with elevate... According to a genome-wide association study,intronic SNPs within the human sterile 20/SPS1-related proline/alanine-rich kinase(SPAK) gene was linked to 20% of the general population and may be associated with elevated blood pressure. As cell volume changes,mammalian SPAK kinases respond to phosphorylate and regulate cation-coupled chloride co-transporter activity. To our knowledge,phosphorylation of upstream with-no-lysine(K)(WNK) kinases would activate SPAK kinases. The activation of WNK-OSR1/SPAK cascade on the kidneys and aortic tissue is related to the development of hypertension. Several regulators of the WNK pathway such as the Kelch kinase protein 3-Cullin 3 E3 ligase,hyperinsulinemia,and low potassium intake to mediate hypertension have been identified. In addition,the SPAK kinases may affect the action of renin-angiotensin-aldosterone system on blood pressure as well. In 2010,two SPAK knock-in and knock-out mouse models have clarified the pathogenesis of lowering blood pressure by influencing the receptors on the kidneys and aortic smooth muscle. More recently,two novel SPAK inhibitors for mice,Stock 1S-14279 and Closantel were discovered in 2014. Targeting of SPAK seems to be promising for future antihypertensive therapy. Therefore we raised some viewpoints for the issue for the antihypertensive therapy on the SPAK(gene or kinase). 展开更多
关键词 With-no-lysine(K) KInaSE Oxidative stressresponsive KInaSE 1/SPS1-related proline/alaninerich KInaSE KInaSE na-cl co-transporter na+-k+-2cl(-) cOTRANSPORTER Hypertension
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大黄-黄芩配伍应用对脑损伤早期癫痫易感性的影响 被引量:4
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作者 施所琴 严瑶瑶 +1 位作者 马瑶 王福顺 《中国实验方剂学杂志》 CAS CSCD 北大核心 2018年第10期168-174,共7页
目的:研究大黄-黄芩配伍应用对小鼠脑损伤早期癫痫易感性的影响,探讨该药对抗脑损伤后癫痫的机制。方法:将SPF级C57BL/6J雄性小鼠随机分为空白组,模型组,大黄-黄芩药对低(1 g·kg^-1),高剂量组(4 g·kg^-1)及阳性组(2.6 ... 目的:研究大黄-黄芩配伍应用对小鼠脑损伤早期癫痫易感性的影响,探讨该药对抗脑损伤后癫痫的机制。方法:将SPF级C57BL/6J雄性小鼠随机分为空白组,模型组,大黄-黄芩药对低(1 g·kg^-1),高剂量组(4 g·kg^-1)及阳性组(2.6 g·kg^-1丙戊酸钠)。除空白组外,其余各组采用自由落体法建立小鼠封闭性颅脑损伤模型,于脑损伤后给予相应药物灌胃治疗,连续7 d。于末次给药后给予戊四氮(pentylenetetrazole,PTZ)亚惊厥剂量刺激,通过行为学观察各组小鼠的癫痫发作潜伏期及平均发作强度,脑电图(electroencephalogram,EEG)分析小鼠的脑部放电图谱,统计0-20 Hz的放电总和;免疫组化法(immunohistochemistry,IHC)计数海马CA1,CA3区胶质纤维酸性蛋白(glial fibrillary acidic protein,GFAP)的阳性细胞数;蛋白免疫印迹法(Western blot)检测神经元Na^+-K^+-2Cl^-共转运体-1(NKCC1)的蛋白表达水平。结果:与空白组比较,模型组的小鼠癫痫发作潜伏期明显缩短,脑部异常高频放电明显增多,海马CA1,CA3区的GFAP阳性细胞计数显著增加(P〈0.05),且神经元NKCC1的表达也较高(P〈0.05);与模型组比较,药对低、高剂量均可延长癫痫发作的潜伏期,减少脑部异常放电,降低海马区GFAP阳性细胞数以及神经元NKCC1蛋白的表达,且药对高剂量组与模型组比较具有显著性差异(P〈0.05)。结论:大黄-黄芩配伍应用可降低脑损伤早期癫痫的易感性,作用机制可能与星形胶质细胞的调控作用有关。 展开更多
关键词 大黄-黄芩 脑损伤后癫痫 胶质纤维酸性蛋白(GFAP) 神经元na+-k+-2cl-共转运体-1(nkcc1) 星形胶质细胞
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