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动物研究中关于局部使用氯沙坦预防和治疗角膜瘢痕纤维化的疗效和安全性的见解。

Insights from animal studies exploring the efficacy and safety of topical losartan, in prophylaxis and treatment of corneal scarring fibrosis.

作者信息

Villabona-Martinez Valeria, Dutra Barbara Araujo Lima, Wilson Steven E

机构信息

The Cole Eye Institute, The Cleveland Clinic, Cleveland, OH 44195, United States.

The Cole Eye Institute, The Cleveland Clinic, Cleveland, OH 44195, United States; Department of Ophthalmology at University of Sao Paulo, Sao Paulo, Brazil.

出版信息

Biomed Pharmacother. 2025 Feb;183:117857. doi: 10.1016/j.biopha.2025.117857. Epub 2025 Jan 17.

Abstract

Several studies in rabbits demonstrated the efficacy and safety of topical losartan, an angiotensin II receptor blockers (ARB) that modulates the TGF-β intracellular signaling pathways by inhibiting the activation of Extracellular Signal-regulated Kinase (ERK), in preventing or treating stromal fibrosis after a range of injuries such as Descemetorhexis, alkali burns, incisions, and photorefractive keratectomy (PRK). Several case reports have shown that topical losartan treatment is also efficacious and safe in humans to prevent or treat stromal fibrosis after many different injuries or diseases. Topical losartan penetrates the full thickness of the cornea and, therefore, can treat both anterior and posterior stromal fibrosis. These rabbit studies have demonstrated that there can be epithelial and stromal toxicity to losartan at dosages greater than 0.8 mg/ml and that higher dosages will not accelerate the return to transparency of fibrotic corneas. In corneas with an epithelial defect, it is likely safer to use 0.2 mg/ml losartan six times a day until the epithelium closes to further decrease the risk of epithelial toxicity before going to the 0.8 mg/ml six times a day dosage. Future clinical studies will explore additional questions, such as whether four times a day dosing is less effective than six times a day dosing in the treatment of stromal fibrosis.

摘要

多项针对兔子的研究表明,局部使用氯沙坦(一种血管紧张素II受体阻滞剂,通过抑制细胞外信号调节激酶(ERK)的激活来调节转化生长因子-β细胞内信号通路)在预防或治疗诸如后弹力层撕脱、碱烧伤、切口以及准分子激光原位角膜磨镶术(PRK)等一系列损伤后的基质纤维化方面具有有效性和安全性。多项病例报告显示,局部使用氯沙坦治疗在人类预防或治疗多种不同损伤或疾病后的基质纤维化方面同样有效且安全。局部使用的氯沙坦可穿透角膜全层,因此能够治疗前部和后部基质纤维化。这些针对兔子的研究表明,剂量大于0.8毫克/毫升时氯沙坦可能会产生上皮和基质毒性,且更高剂量并不会加速纤维化角膜恢复透明。对于存在上皮缺损的角膜,在上皮愈合之前,每天使用6次0.2毫克/毫升的氯沙坦可能更安全,以进一步降低上皮毒性风险,之后再改为每天6次0.8毫克/毫升的剂量。未来的临床研究将探讨其他问题,例如每天给药4次在治疗基质纤维化方面是否比每天给药6次效果差。

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