能量基质补充会增加ATP水平,并对PD神经元有保护作用
Andrey Y Vinokurov1, Marina Y Pogonyalova1, Larisa Andreeva2
1Cell Physiology and Pathology Laboratory, Orel State University, Orel, Russia.
Current research in pharmacology and drug discovery
|June 6, 2024
概括
使用特定基质恢复细胞能量生产,可以保护大脑细胞免受神经退行. 补充胆酸盐和尼古丁胺的组合证明在提高ATP水平和预防细胞死亡方面最有效.
科学领域:
- 神经科学是一个神经科学.
- 细胞的新陈代谢
- 生物化学 生物化学
背景情况:
- 线粒体功能障碍和能量代谢的改变与神经系统疾病和神经退行性疾病有关.
- 恢复ATP生产和用能量基质补充大脑细胞的神经保护潜力仍然不清楚.
研究的目的:
- 调查能量代谢基质是否可以增强神经元功能和神经元和星球细胞中的ATP产生.
- 为了确定增加的ATP水平是否能提供对谷氨酸兴奋毒性和神经退行症的保护.
- 在家族性帕金森病的细胞模型中评估这些干预措施的疗效.
主要方法:
- 用TCA循环,细胞呼吸和氧化酸化的各种基质补充初级神经元和星球细胞.
- 利用了家族性神经退行性疾病的细胞模型,包括帕金森病.
- 评估了线粒体的NADH水平,线粒体膜潜力和ATP生产.
- 评估了细胞对诱导性缺血和谷氨酸刺激毒性的保护.
主要成果:
- 基质补充显著增加了线粒体的NADH水平和膜潜力,导致神经元和星体细胞的ATP产生更高.
- 增强的ATP水平保护细胞在缺血和谷氨酸兴奋毒性期间免受能量剥夺.
- 用能量基质补充剂在家族帕金森病模型中预防了细胞死亡.
结论:
- 恢复细胞能量代谢和增加ATP生产表明神经退行过程中神经保护作用.
- 胆酸和尼古丁胺的组合产生了最重要的神经保护作用.
更多相关视频
06:07Author Spotlight: Establishing a New Fluorescence-Based Protocol for In Vivo Mitochondrial Morphology Analysis in Parkinson's Disease
Published on: June 23, 2023
1.5K
11:20Imaging of Intracellular ATP in Organotypic Tissue Slices of the Mouse Brain using the FRET-based Sensor ATeam1.03YEMK
Published on: December 19, 2019
9.7K
相关概念视频
Muscle Recovery and Fatigue
2.1K
Muscle fatigue refers to the decline in a muscle's ability to maintain the force of contraction after prolonged activity. It primarily stems from changes within muscle fibers. Even before experiencing muscle fatigue, one may feel tired and have the urge to stop the activity. This response, known as central fatigue, occurs due to changes in the central nervous system, namely the brain and spinal cord. While there is no single mechanism that induces fatigue, it may serve as a protective...
2.1K
Energy Supply for Muscle Contraction
3.1K
Skeletal muscle fibers have the unique ability to switch between rest and contraction states, using different sources of ATP for energy. The contraction cycle and Ca2+ transport back into the sarcoplasmic reticulum for relaxation require significant ATP. However, the ATP reserves in muscle fibers are limited and can only sustain contractions for a few seconds. Additional ATP production becomes necessary for prolonged contractions. As a result, muscle fibers generate ATP through various sources,...
3.1K
ATP Synthase: Mechanism
14.5K
In animals, the mitochondrial F1F0 ATP synthase is the key protein that synthesizes ATP molecules through a complex catalytic mechanism. While the nuclear genome encodes the majority of ATP synthase subunits, the mitochondrial genome encodes some of the enzyme's most critical components. The formation of this multi-subunit enzyme is a complex multi-step process regulated at the level of transcription, translation, and assembly. Defects in one or more of these steps can result in decreased...
14.5K
ATP Energy Storage and Release
9.3K
ATP is a highly unstable molecule. Unless quickly used to perform work, ATP spontaneously dissociates into ADP and inorganic phosphate (Pi), and the free energy released during this process is lost as heat. The energy released by ATP hydrolysis is used to perform work inside the cell and depends on a strategy called energy coupling. Cells couple the exergonic reaction of ATP hydrolysis with endergonic reactions, allowing them to proceed.
One example of energy coupling using ATP involves a...
One example of energy coupling using ATP involves a...
9.3K
ATP Driven Pumps I: An Overview
8.1K
ATP-driven pumps, also known as transport ATPases, are integral membrane proteins. They have binding sites for ATP located on the membrane's cytosolic side and the ion-conducting domain in the transmembrane region. These pumps use the free energy released from ATP hydrolysis to move the solutes across cell membranes against an electrochemical gradient.
There are four main types of ATP-driven pumps - P-type, V-type, F-type, and ABC transporter. All these pumps are of varying complexities and...
There are four main types of ATP-driven pumps - P-type, V-type, F-type, and ABC transporter. All these pumps are of varying complexities and...
8.1K
Electron Transport Chain: Complex I and II
13.0K
The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
ROS generation is regulated and maintained at moderate levels necessary...
13.0K
