Nenicu Anca, Gu Yuan, Körbel Christina, Menger Michael D, Laschke Matthias W
Institute for Clinical & Experimental Surgery, Saarland University, Homburg/Saar, Germany.
Br J Pharmacol. 2017 Aug;174(16):2623-2635. doi: 10.1111/bph.13874. Epub 2017 Jul 6.
Telmisartan suppresses the development of endometriotic lesions. However, the drug also up-regulates the expression of COX-2, which has been suggested to promote the progression of endometriosis. Accordingly, in the present study we analysed whether a combination therapy with telmisartan and a COX-2 inhibitor may be more effective in the treatment of endometriotic lesions than the application of telmisartan alone.
Endometriotic lesions were induced in the peritoneal cavity of C57BL/6 mice, which were treated daily with an i.p. injection of telmisartan (10 mg·kg ), parecoxib (5 mg·kg ), a combination of telmisartan and parecoxib or vehicle. Therapeutic effects on lesion survival, growth, vascularization, innervation and protein expression were studied over 4 weeks by high-resolution ultrasound imaging as well as immunohistochemical and Western blot analyses.
Telmisartan-treated lesions exhibited a significantly reduced lesion volume when compared with vehicle-treated controls and parecoxib-treated lesions. This inhibitory effect of telmisartan was even more pronounced when it was used in combination with parecoxib. The combination therapy resulted in a reduced microvessel density as well as lower numbers of proliferating Ki67-positive cells and higher numbers of apoptotic cleaved caspase-3-positive stromal cells within the lesions. This was associated with a lower expression of COX-2, MMP-9 and p-Akt/Akt when compared with controls. The application of the two drugs further inhibited the ingrowth of nerve fibres into the lesions.
Combination therapy with telmisartan and a COX-2 inhibitor represents a novel, effective pharmacological strategy for the treatment of endometriosis.
替米沙坦可抑制子宫内膜异位症病灶的发展。然而,该药物也会上调环氧化酶-2(COX-2)的表达,而COX-2被认为会促进子宫内膜异位症的进展。因此,在本研究中,我们分析了替米沙坦与COX-2抑制剂联合治疗在子宫内膜异位症病灶治疗中是否比单独使用替米沙坦更有效。
在C57BL/6小鼠的腹腔内诱导产生子宫内膜异位症病灶,每天通过腹腔注射替米沙坦(10mg·kg)、帕罗西汀(5mg·kg)、替米沙坦与帕罗西汀的组合或赋形剂进行治疗。通过高分辨率超声成像以及免疫组织化学和蛋白质印迹分析,在4周内研究对病灶存活、生长、血管生成、神经支配和蛋白质表达的治疗效果。
与赋形剂处理的对照组和帕罗西汀处理的病灶相比,替米沙坦处理的病灶体积显著减小。当替米沙坦与帕罗西汀联合使用时,这种抑制作用更加明显。联合治疗导致病灶内微血管密度降低,增殖的Ki67阳性细胞数量减少,凋亡的裂解型半胱天冬酶-3阳性基质细胞数量增加。与对照组相比,这与COX-2、基质金属蛋白酶-9和磷酸化Akt/Akt的表达降低有关。两种药物的应用进一步抑制了神经纤维向病灶内的生长。
替米沙坦与COX-2抑制剂联合治疗是一种治疗子宫内膜异位症的新型有效药理学策略。