动脉样硬化潜在药物点:当前情景和未来前景
Omar Mohammed Ali Saleh Al Qarawani1, Palwinder Kaur1, Manish Vyas1
1Department of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab, 144401, India.
Cardiovascular & hematological disorders drug targets
|October 27, 2023
概括
动脉样硬化仍然是导致死亡的主要原因. 新的研究探索了细胞和分子点,包括遗传学和免疫细胞,以开发针对这种广泛的心血管疾病的改进治疗方法.
科学领域:
- 心血管生物学 心血管生物学
- 分子医学是分子医学.
背景情况:
- 动脉样硬化是全球疾病和死亡的主要原因,包括在美国和欧洲.
- 尽管在诊断和早期干预方面取得了进展,但有效的长期治疗动脉样硬化仍然是一个挑战.
研究的目的:
- 审查目前对动脉样硬化病理生理学的理解.
- 突出新兴的治疗策略和动脉样硬化管理的目标.
- 讨论与动脉样硬化治疗相关的细胞和分子生物学最近的发现.
主要方法:
- 对当前病理生理机制的文献综述.
- 对现有治疗剂的局限性进行分析.
- 探索新的分子和细胞目标.
主要成果:
- 常规治疗动脉样硬化有其局限性.
- 新兴的策略显示出对更有效的疾病管理有希望.
- 遗传因素,免疫细胞和非编码RNA是未来治疗开发的关键领域.
结论:
- 对分子和细胞机制的进一步研究对于推进动脉样硬化治疗至关重要.
- 识别新的生物标志物和药物标可以导致更好的药理学药剂和输送系统.
- 针对遗传倾向和免疫反应,为控制动脉样硬化发病率和流行率提供了一个有希望的未来方向.
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