Effect of repaglinide on cloned beta cell, cardiac and smooth muscle types of ATP-sensitive potassium channels.

Author: AshcroftF M, DabrowskiM, HolmesW E, WahlP

Paper Details 
Original Abstract of the Article :
The carbamoylbenzoic acid derivative repaglinide is a potent short-acting insulin secretagogue that acts by closing ATP-sensitive potassium (KATP) channels in the plasma membrane of the pancreatic beta cell. In this paper we investigated. the specificity of repaglinide for three types of cloned (KAT...See full text at original site
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引用元:
https://doi.org/10.1007/s001250051684

データ提供:米国国立医学図書館(NLM)

Repaglinide and KATP Channels: A Journey Through Molecular Interactions

Dr. Camel, a curious explorer of the human body's intricate mechanisms, is fascinated by the delicate dance between molecules. This research dives into the fascinating world of molecular interactions, specifically focusing on the interaction between the insulin secretagogue repaglinide and different subtypes of ATP-sensitive potassium (KATP) channels. The study investigated the specificity of repaglinide for three types of cloned KATP channels: those found in pancreatic beta cells, cardiac muscle, and smooth muscle.

The researchers investigated the effects of repaglinide on cloned KATP channels composed of the inwardly rectifying potassium channel Kir6.2 and either the sulphonylurea receptor SUR1, SUR2A, or SUR2B. They found that repaglinide exhibited a significant affinity for the beta cell type of KATP channel (Kir6.2/SUR1), consistent with its known role in insulin secretion. However, the study revealed that repaglinide also interacted with the cardiac type (Kir6.2/SUR2A) and the smooth muscle type (Kir6.2/SUR2B) of KATP channels, albeit to a lesser extent. These findings suggest that repaglinide may have additional effects beyond its primary role in insulin secretion, potentially impacting cardiovascular function.

A Complex Landscape of Molecular Interactions

This research highlights the complexity of molecular interactions and the potential for drugs to interact with multiple targets, even those outside their primary therapeutic focus. It's like navigating a vast desert, where the path of a single molecule can lead to unexpected destinations and interactions. The study's findings underscore the importance of understanding these interactions for developing drugs with targeted therapeutic effects and minimizing unintended consequences.

Navigating the Desert of Drug Discovery with Precision

Dr. Camel encourages researchers to continue exploring the intricate pathways of molecular interactions to develop drugs with precise therapeutic effects. This research provides valuable insights into the complex landscape of drug-receptor interactions, reminding us that even seemingly targeted drugs can have broader effects. It's like having a map guiding you through the desert of drug discovery, helping you navigate the complex terrain and reach your desired destination with greater precision.

Dr. Camel's Conclusion

This research delves into the complex interplay between repaglinide and different subtypes of KATP channels, highlighting the importance of understanding drug-receptor interactions for developing targeted therapies and minimizing unintended consequences. It's like uncovering a hidden oasis of knowledge in the vast desert of drug discovery, offering valuable insights for researchers seeking to develop more effective and safe treatments.

Date :
  1. Date Completed 2001-12-05
  2. Date Revised 2022-04-08
Further Info :

Pubmed ID

11440368

DOI: Digital Object Identifier

10.1007/s001250051684

Related Literature

SNS
PICO Info
in preparation
Languages

English

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