斯芬哥辛激酶1抑制加剧了血管光滑肌肉细胞化
Mehdi Razazian1, Sheyda Bahiraii1, Isratul Jannat1
1Institute for Physiology and Pathophysiology, Johannes Kepler University Linz, Krankenhausstrasse 5, 4020, Linz, Austria.
Pflugers Archiv : European journal of physiology
|February 3, 2025
概括
抑制斯芬哥辛激酶1 (SPHK1) 在光滑肌细胞和小鼠中加剧了血管化. 阻止S1P的输出减少了化,这表明细胞内S1P信号在血管化中起作用.
科学领域:
- 血管生物学 血管生物学
- 细胞信号传递 细胞信号传递
- 矿物质的新陈代谢.
背景情况:
- 中部血管化在慢性病中很普遍,与高酸血症有关.
- 血管光滑肌细胞 (VSMCs) 在对酸盐的反应中调解亲性信号.
- 斯芬戈基因酶1 (SPHK1) 产生具有复杂血管作用的斯芬戈-1-酸盐 (S1P).
研究的目的:
- 研究SPHK1在VSMC化中的作用.
- 确定SPHK1抑制和S1P出口调节对血管化的影响.
主要方法:
- 在特定条件下对人类主动脉VSMC进行实验.
- 药理上抑制或消除SPHK1和SPNS2 (S1P出口者).
- 在Sphk1缺乏和野生类型小鼠中进行过多胆氨醇负载的研究.
主要成果:
- 随着特定条件的出现,SPHK1的表达增加.
- SPHK1抑制或淘汰加剧VSMC化和骨质生成信号.
- 抑制S1P出口 (SPNS2) 抑制了VSMC化,取决于SPHK1.
- 在小鼠中,Sphk1缺乏会使血管化恶化.
结论:
- SPHK1的抑制,淘汰或缺乏会加剧血管前性信号和化.
- 阻断S1P出口后减少化表明细胞内S1P的作用.
- 需要进一步的研究来澄清SPHK和S1P在VSMC化中的复杂作用.
相关概念视频
Antihypertensive Drugs: Action of Calcium Channel Blockers
446
Calcium ions are essential to contract smooth muscle cells in blood vessels. They enter these cells through voltage-dependent calcium channels, specifically L-type calcium channels in the cell membrane. These L-type calcium channels are integral to the excitation-contraction coupling process in smooth muscle. When a stimulus is received by smooth muscle cells, their membrane depolarizes. This alteration in membrane potential instigates the opening of L-type calcium channels. As a result,...
446
Antihypertensive Drugs: Vasodilators
463
Vasodilators, primarily affecting the smooth muscles within arterial and venous walls, are commonly used for hypertension treatment. Medications such as minoxidil and hydralazine primarily target arteries and arterioles, while sodium nitroprusside acts on arterioles and venules. Minoxidil, functioning as a prodrug, is metabolized by hepatic sulfotransferase into its active form, minoxidil sulfate, after oral administration. This metabolite binds to the sulfonylurea receptor (SUR) component of...
463
Nitric Oxide Signaling Pathway
4.9K
Nitric oxide (NO), an inorganic gas, acts as a potent second messenger in most animal and plant tissues. NO diffuses out of the cells that produce it and enters the neighboring cells to generate a downstream response. NO synthase (NOS) catalyzes NO production by the deamination of the amino acid arginine. There are three isoforms of NOS. Endothelial cells have endothelial NOS (eNOS), nerve and muscle cells have neuronal NOS (nNOS), and macrophages produce inducible NOS (iNOS) upon exposure...
4.9K
Phosphoinositides and PIPs
8.3K
Phosphoinositides are a group of phospholipids containing a glycerol backbone with two fatty acid chains and a phosphate attached to a myoinositol sugar ring. The inositol head group extends into the cytoplasm, where it is modified by adding phosphate groups to form phosphatidylinositol phosphates or PIPs.
Different phosphoinositides are synthesized and recruited on the cytosolic face of the plasma membrane. The localization of specific phosphoinositides concentrated in separate membrane...
Different phosphoinositides are synthesized and recruited on the cytosolic face of the plasma membrane. The localization of specific phosphoinositides concentrated in separate membrane...
8.3K
Vascular Spasm
1.2K
The vascular phase, also known as vasospasm, is the initial stage of hemostasis, crucial for preventing excessive bleeding when a blood vessel is injured. After a vessel is cut, nerves in the damaged area trigger pain and other sensory impulses. Simultaneously, the smooth muscles in the vessel wall contract, resulting in a vascular spasm. This contraction reduces the vessel's diameter at the injury site, slowing or stopping blood loss through the vessel wall. Vascular spasms typically last...
1.2K


