Sun Jingchao, Xiao Ying, Xu Wenjie, Xing Wei, Du Frank, Tian Maozhi, Xu Danqi, Ren Yihua, Fang Xin
R&D Center, Shenzhen Salubris Pharmaceutical Co., Ltd., Shenzhen, Guangdong, China.
iBHE, Tsinghua Shenzhen International Graduate School, Shenzhen, Guangdong, China.
Front Cardiovasc Med. 2024 Feb 14;11:1348897. doi: 10.3389/fcvm.2024.1348897. eCollection 2024.
Angiotensin receptor-neprilysin inhibitor (ARNi), comprised of an angiotensin receptor blocker (ARB) and a neprilysin inhibitor (NEPi), has established itself as a safe and effective intervention for hypertension. S086 is a novel ARNi cocrystal developed by Salubris for the treatment of heart failure and hypertension.
Dahl Salt Sensitive (DSS) hypertensive rat model and telemetry system were employed in this study to investigate the anti-hypertensive efficacy of S086 and compare it with the first ARNi-LCZ696.
The study showed that oral administration of S086 dose-dependently lowered blood pressure ( < 0.001). The middle dosage of S086 (23 mg/kg) exhibited efficacy comparable to LCZ696 (68 mg/kg), while also demonstrating superiority at specific time points ( < 0.05). Notably, water consumption slightly decreased post-treatment compared to the vehicle group. Furthermore, there were significant increases in natriuresis and diuresis observed on the first day of treatment with 23 mg/kg and 68 mg/kg S086 ( < 0.001). However, over the course of treatment, the effects in all treatment groups gradually diminished. This study demonstrates the anti-hypertensive efficacy of S086 in DSS hypertensive rat model, offering promising avenues for the clinical development of S086 as a hypertension treatment.
血管紧张素受体脑啡肽酶抑制剂(ARNi)由血管紧张素受体阻滞剂(ARB)和脑啡肽酶抑制剂(NEPi)组成,已成为治疗高血压的一种安全有效的干预措施。S086是由信立泰研发的一种新型ARNi共晶体,用于治疗心力衰竭和高血压。
本研究采用 Dahl 盐敏感(DSS)高血压大鼠模型和遥测系统,研究 S086 的降压疗效,并与首个 ARNi-LCZ696 进行比较。
研究表明,口服 S086 可剂量依赖性降低血压(<0.001)。S086 的中剂量(23 mg/kg)表现出与 LCZ696(68 mg/kg)相当的疗效,同时在特定时间点也显示出优势(<0.05)。值得注意的是,与赋形剂组相比,治疗后水消耗量略有下降。此外,在使用 23 mg/kg 和 68 mg/kg S086 治疗的第一天,观察到尿钠排泄和利尿显著增加(<0.001)。然而,在治疗过程中,所有治疗组的效果逐渐减弱。本研究证明了 S086 在 DSS 高血压大鼠模型中的降压疗效,为 S086 作为高血压治疗药物的临床开发提供了有前景的途径。