Selexipag: a selective prostacyclin receptor agonist that does not affect rat gastric function.

Author: ClozelMartine, ErnstRoland, HessPatrick, MorrisonKeith, StuderRolf

Paper Details 
Original Abstract of the Article :
Selexipag [2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-N-(methylsulfonyl)acetamide] is an orally available prostacyclin (PGI(2)) receptor (IP receptor) agonist that is chemically distinct from PGI(2) and is in clinical development for the treatment of pulmonary arterial hypertension. Se...See full text at original site
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引用元:
https://doi.org/10.1124/jpet.110.169748

データ提供:米国国立医学図書館(NLM)

Selexipag: A Selective Prostacyclin Receptor Agonist That Does Not Affect Rat Gastric Function

This research delves into the realm of [pulmonary arterial hypertension (PAH)] treatment and the potential benefits of a novel [prostacyclin receptor agonist], selexipag. Much like a camel navigating a desert landscape searching for a source of water, researchers investigated the effects of selexipag on the [gastric function] of rats. The study found that selexipag, unlike other prostacyclin analogs, did not cause [gastric contraction] or affect [gastric emptying and intestinal transport], suggesting a favorable safety profile in terms of minimizing [gastrointestinal side effects] like nausea and vomiting. This study offers a potential solution for the management of PAH while minimizing gastrointestinal side effects.

Selexipag: A Promising Option for PAH with a Favorable Gastrointestinal Profile

This study highlights the potential of selexipag as a promising treatment option for PAH, as it demonstrates efficacy in activating the IP receptor while minimizing potential gastrointestinal side effects. The researchers found that selexipag did not affect gastric function in rats, unlike other prostacyclin analogs, suggesting a potential advantage for patients who may experience gastrointestinal discomfort with other treatments.

Navigating PAH Treatment: Seeking a Balance Between Efficacy and Safety

This study emphasizes the importance of balancing efficacy and safety in PAH treatment. The research suggests that selexipag may offer a favorable gastrointestinal profile compared to other prostacyclin analogs, potentially improving patient comfort and adherence to treatment. This research encourages further exploration of selexipag's potential as a safe and effective treatment for PAH.

Dr. Camel's Conclusion

This research, much like a camel seeking a safe passage through a desert landscape, explores the potential of selexipag as a promising treatment option for PAH. The study's findings suggest that selexipag, unlike other prostacyclin analogs, does not affect gastric function in rats, potentially reducing the risk of gastrointestinal side effects. This research offers valuable insights into the potential benefits of selexipag as a safe and effective treatment option for PAH, paving the way for improved management of this challenging condition.

Date :
  1. Date Completed 2010-10-21
  2. Date Revised 2017-11-16
Further Info :

Pubmed ID

20660124

DOI: Digital Object Identifier

10.1124/jpet.110.169748

SNS
PICO Info
in preparation
Languages

English

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