质子感应G蛋白合受体及其在运动调节动脉功能的潜在作用
Fengzhi Yu1, Dandan Jia1, Ru Wang1
1School of Exercise and Health, Shanghai University of Sport, Shanghai 200438, China.
Biomolecules
|June 26, 2025
概括
运动通过改变质子度影响动脉pH值,影响质子感应G蛋白合受体. 这项研究探讨了炼运动.
科学领域:
- 生理学 生理学 生理学
- 生物化学 生物化学
- 药理学 药理学是指药理学的学科.
背景情况:
- 运动通过乳酸盐和CO2的轻微呼吸系统酸性酶诱导代谢酸性酶,轻微降低动脉血液pH值.
- 质子感应G蛋白合受体 (GPR68,GPR4,GPR132,GPR65) 检测细胞外质子变化并影响各种生理过程.
- 这些受体参与动脉功能,如血管生成,放松和炎症,运动已知有利于动脉健康.
研究的目的:
- 研究运动如何影响微环境质子度.
- 检查运动诱导的质子变化对质子感应G蛋白合受体的影响.
- 探索通过这些受体和运动调节动脉功能的潜在机制.
主要方法:
- 对运动诱导的细胞外质子度变化的分析.
- 研究质子感应G蛋白合受体的调制.
- 探索动脉功能调节的潜在机制.
主要成果:
- 运动会改变微环境中的质子度.
- 质子感应G蛋白合受体受到这些运动诱导的质子转移的影响.
- 确定了运动,质子传感和动脉功能调节之间的潜在机制.
结论:
- 运动显著影响质子微环境及其感知受体.
- 这种相互作用为维持动脉功能提供了新的见解.
- 研究结果表明,对于动脉功能障碍和炼方案的开发,有潜在的治疗点.
更多相关视频
09:04Skeletal Muscle Neurovascular Coupling, Oxidative Capacity, and Microvascular Function with 'One Stop Shop' Near-infrared Spectroscopy
Published on: February 20, 2018
12.7K
12:37Surgical Placement of Catheters for Long-term Cardiovascular Exercise Testing in Swine
Published on: February 9, 2016
13.5K
相关概念视频
G-Protein Gated Ion Channels
4.9K
GPCRs are primarily responsible for our sense of smell, taste, and vision. The binding of a sensory stimulus activates GPCR to stimulate effector proteins, many of which are ion channels in the sensory organs. GPCRs modulate the opening and closing of the target ion channels either directly by binding them, or by releasing second messengers that activate these channels. As ions move across the membrane, the membrane potential is altered, which induces an appropriate response.
Sensory...
Sensory...
4.9K
G-protein Coupled Receptors
121.8K
G-protein coupled receptors are ligand binding receptors that indirectly affect changes in the cell. The actual receptor is a single polypeptide that transverses the cell membrane seven times creating intracellular and extracellular loops. The extracellular loops create a ligand specific pocket which binds to neurotransmitters or hormones. The intracellular loops holds onto the G-protein.
121.8K
Transducer Mechanism: Enzyme-Linked Receptors
2.8K
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
Major types that are helpful drug targets include:
2.8K
Regulation of the Cardiovascular System
2.0K
The regulation of the cardiovascular system allows the body to adapt to various demands and maintain homeostasis.
The regulation of the cardiovascular system involves the autonomic nervous system (ANS), baroreceptors, and chemoreceptors, ensuring that heart rate and blood pressure are appropriately modulated in response to varying physiological demands.
The ANS comprises two main divisions: the sympathetic and parasympathetic nervous systems. The sympathetic nervous system enhances...
The regulation of the cardiovascular system involves the autonomic nervous system (ANS), baroreceptors, and chemoreceptors, ensuring that heart rate and blood pressure are appropriately modulated in response to varying physiological demands.
The ANS comprises two main divisions: the sympathetic and parasympathetic nervous systems. The sympathetic nervous system enhances...
2.0K
G Protein-coupled Receptors
13.6K
G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
13.6K
Activation and Inactivation of G Proteins
7.7K
Heterotrimeric G proteins are guanine nucleotide-binding proteins. As the name suggests, heterotrimeric G proteins are composed of three subunits: alpha, beta, and gamma. They remain GDP-bound or GTP-bound inside the cells and switch between inactive/active states. The Gα subunit possesses the nucleotide-binding pocket that binds guanine nucleotides and switches between GDP or GTP-bound states. In contrast, the Gꞵ and Gγ subunits are always bound together with high...
7.7K
