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慢性西那卡塞可提高大鼠皮瓣存活率:一氧化氮通路的作用。

Chronic Cinacalcet improves skin flap survival in rats: the suggested role of the nitric oxide pathway.

机构信息

Department of Pharmacology, School of Medicine, AJA University of Medical Sciences, Tehran, Iran.

Toxicology Research Center, AJA University of Medical Sciences, Tehran, Iran.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2024 Jul;397(7):5005-5013. doi: 10.1007/s00210-023-02922-7. Epub 2024 Jan 6.

Abstract

Cinacalcet is a calcimimetic medicine that has been used to treat secondary hyperparathyroidism and parathyroid cancer. Various studies have proposed the positive role of calcium and its receptor in skin wound healing. Furthermore, Cinacalcet interacts with other skin repair-related mechanisms, including inflammation and nitric oxide pathways. The present study evaluated the effect of Cinacalcet on the random-pattern skin flap survival. Eighty-four Wistar male rats were used. Multiple doses of Cinacalcet (30, 3, 1, 0.3, and 0.05 mg/kg) were used in 3 different routes of administration before the surgery. Histopathological evaluations, quantitative assessment of IL-6, TNF-α, and nitric oxide (NO), and the expression of calcium-sensing receptor (CaSR) and E-cadherin were evaluated in the skin tissue. To assess the role of NO, a NO synthase inhibitor, N-nitro-L-arginine methyl ester hydrochloride (L-NAME), was used, and histopathological effects were investigated. Cinacalcet pretreatment at the IP chronic 1 mg/kg dose significantly increased the skin flap survival rate and enhanced the NO tissue level compared to the control. However, the administration of L-NAME abolished its protective effects. IP Chronic 1 mg/kg of Cinacalcet could also decline the levels of IL-6 and TNF-α and also increase the expression of CaSR and E-cadherin in the flap tissue compared with the control group. Chronic Cinacalcet at 1 mg/kg could improve skin flap survival, probably mediated by the CaSR, NO, and inflammation-related pathways.

摘要

西那卡塞是一种拟钙剂药物,已被用于治疗继发性甲状旁腺功能亢进和甲状旁腺癌。多项研究提出了钙及其受体在皮肤伤口愈合中的积极作用。此外,西那卡塞与其他与皮肤修复相关的机制相互作用,包括炎症和一氧化氮途径。本研究评估了西那卡塞对随意皮瓣存活的影响。使用了 84 只 Wistar 雄性大鼠。在手术前,通过 3 种不同的给药途径使用了多种剂量的西那卡塞(30、3、1、0.3 和 0.05mg/kg)。对皮肤组织进行了组织病理学评估、IL-6、TNF-α 和一氧化氮(NO)的定量评估,以及钙敏感受体(CaSR)和 E-钙粘蛋白的表达评估。为了评估 NO 的作用,使用了一氧化氮合酶抑制剂 N-硝基-L-精氨酸甲酯盐酸盐(L-NAME),并研究了其组织学效应。与对照组相比,IP 慢性 1mg/kg 西那卡塞预处理显著提高了皮瓣存活率,并增强了组织中 NO 水平。然而,L-NAME 的给药消除了其保护作用。与对照组相比,IP 慢性 1mg/kg 西那卡塞还可以降低皮瓣组织中 IL-6 和 TNF-α 的水平,并增加 CaSR 和 E-钙粘蛋白的表达。慢性西那卡塞 1mg/kg 可通过 CaSR、NO 和炎症相关途径改善皮瓣存活。

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