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"NO" controversy?: A controversial role in insulin signaling of diabetic encephalopathy.
Chen, Xi; Song, Ying; Hong, Ye; Zhang, Xiaomin; Li, Qisong; Zhou, Hongling.
Afiliación
  • Chen X; Department of Pharmacology, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
  • Song Y; Department of Pharmacology, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China; Hangzhou King's Bio-pharmaceutical Technology Co., Ltd, Hangzhou, Zhejiang, 310007, China. Electronic address: songying@zjut.edu.cn.
  • Hong Y; Department of Pharmacology, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
  • Zhang X; Department of Pharmacology, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
  • Li Q; Department of Pharmacology, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
  • Zhou H; Department of Pharmacology, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
Mol Cell Endocrinol ; 593: 112346, 2024 Nov 01.
Article en En | MEDLINE | ID: mdl-39151653
ABSTRACT
Insulin, a critical hormone in the human body, exerts its effects by binding to insulin receptors and regulating various cellular processes. While nitric oxide (NO) plays an important role in insulin secretion and acts as a mediator in the signal transduction pathway between upstream molecules and downstream effectors, holds a significant position in the downstream signal network of insulin. Researches have shown that the insulin-NO system exhibits a dual regulatory effect within the central nervous system, which is crucial in the regulation of diabetic encephalopathy (DE). Understanding this system holds immense practical importance in comprehending the targets of existing drugs and the development of potential therapeutic interventions. This review extensively examines the characterization of insulin, NO, Nitric oxide synthase (NOS), specific NO pathway, their interconnections, and the mechanisms underlying their regulatory effects in DE, providing a reference for new therapeutic targets of DE.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Óxido Nítrico Sintasa / Insulina / Óxido Nítrico Límite: Animals / Humans Idioma: En Revista: Mol Cell Endocrinol Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Óxido Nítrico Sintasa / Insulina / Óxido Nítrico Límite: Animals / Humans Idioma: En Revista: Mol Cell Endocrinol Año: 2024 Tipo del documento: Article País de afiliación: China
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