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The selective PGI2 receptor agonist selexipag ameliorates Sugen 5416/hypoxia-induced pulmonary arterial hypertension in rats.
Author: FuchikamiChiaki, HondaYohei, KosugiKeiji, KuramotoKazuya, KuwanoKeiichi, NumakuraYuki
Original Abstract of the Article :
Pulmonary arterial hypertension (PAH) is a lethal disease characterized by a progressive increase in pulmonary artery pressure due to an increase in vessel tone and occlusion of vessels. The endogenous vasodilator prostacyclin and its analogs are used as therapeutic agents for PAH. However, their ph...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561119/
データ提供:米国国立医学図書館(NLM)
Selexipag: A Promising Treatment for Pulmonary Arterial Hypertension
This research takes us on a journey into the challenging world of [cardiology], specifically focusing on the treatment of [pulmonary arterial hypertension (PAH)]. This condition, like a desert sandstorm that constricts the airways, can severely impact lung function and quality of life. The researchers investigated the effectiveness of [selexipag], a [selective prostacyclin receptor agonist], in a rat model of PAH. This approach, akin to meticulously studying the effects of a desert plant on a specific ecosystem, allowed them to gain valuable insights into the potential of selexipag in managing PAH. Their findings suggest that selexipag might be a promising treatment option for PAH, offering a ray of hope for individuals grappling with this challenging condition.Unlocking the Power of Selexipag
The study revealed that selexipag, a [selective prostacyclin receptor agonist], demonstrated significant improvements in reducing pulmonary artery pressure and right ventricular hypertrophy in rats with PAH. This finding, like a well-spring discovered in a barren desert, offers valuable insights into the potential of selexipag as a treatment option for PAH.Living Well with Pulmonary Arterial Hypertension
This research provides a glimmer of hope for individuals living with PAH. The study suggests that selexipag might offer a promising treatment option for this challenging condition. It is crucial to consult with a qualified cardiologist to determine the best course of treatment, as the journey of PAH management is unique for each individual.Dr.Camel's Conclusion
This research offers a ray of hope in the challenging world of pulmonary arterial hypertension. The authors meticulously investigated the effectiveness of selexipag in a rat model of PAH, revealing its potential to reduce pulmonary artery pressure and right ventricular hypertrophy. Like a skilled desert navigator discovering a new route, this research opens up new possibilities for managing PAH and improving the quality of life for those affected by this condition.Date :
- Date Completed 2020-12-09
- Date Revised 2020-12-14
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