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Mechanistic Pathways of ATP Sensitive Potassium Channels Referring to Cardio-Protective Effects and Cellular Functions

Authors :
Tarique Mahmood Ansari
Vivek Srivastava
Hridaya Shanker Chaurasiya
Vishal Kumar Vishwakarma
Ritesh Kumar Srivasatav
Prabhat Kumar Upadhyay
Source :
Drug Research. 69:365-373
Publication Year :
2019
Publisher :
Georg Thieme Verlag KG, 2019.

Abstract

A study of potassium channels correlates the fundamentals of mechanistic pathways and various physiological functions. The knowledge of these pathways provides the background, how to determine unit cell functions and to affect cardio protection. ATP sensitive potassium channels adjust excitability of membrane and functions as per metabolic status of cell. A lot of energy consumption primarily occurred in skeletal muscles which also express high number of potassium channels. The increase in calcium release and high heat production is occurred due to loss of potassium channels. Such type of mediations determines metabolic changes and energy required in the dissipation. IPC reduces infarct size in anesthetized mice. In ischemic-reperfusion, pressure in left ventricle was watched while contractile power recovery did not happen. It was seen that elements of intact potassium channel are fundamental for Ischemic preconditioning (IPC). If more prominent is enactment of potassium channels and their cardiologic effects create high heart rate. All the more as of late, it has been suggested that mitochondrial ATP sensitive potassium channels are critical as closing stage effectors which trigger IPC as opposed to sarcolemmal potassium channels. Nevertheless, the importance of the potassium channels reconsidered in cardio-protection in present findings. These discoveries recommend that potassium channels in the adjusting ischemic-reperfusion damage in mice. The heart rate of the mouse occurred during ischemia; enhance watchful extrapolation applied to larger warm blooded animals.

Details

ISSN :
21949387 and 21949379
Volume :
69
Database :
OpenAIRE
Journal :
Drug Research
Accession number :
edsair.doi.dedup.....0250e72c2ab85a5fffa9c11fa929c500
Full Text :
https://doi.org/10.1055/a-0806-7207