Cámara-Lemarroy Carlos R, Guzmán-de la Garza Francisco J, Cordero-Pérez Paula, Alarcón-Galván Gabriela, Torres-Gonzalez Liliana, Muñoz-Espinosa Linda E, Fernández-Garza Nancy E
Departamento de Fisiología, Facultad de Medicina, UANL, Avenida Francisco I. Madero y Dr. Eduardo Aguirre Pequeño S/No, Col. Mitras Centro, 64460 Monterrey, NL, Mexico.
ScientificWorldJournal. 2011;11:1886-92. doi: 10.1100/2011/583603. Epub 2011 Oct 24.
Ischemia/reperfusion (I/R) is a condition that stimulates an intense inflammatory response. No ideal treatment exists. Triflusal is an antiplatelet salicylate derivative with anti-inflammatory effects. S-adenosylmethionine is a metabolic precursor for glutathione, an endogenous antioxidant. Dextromethorphan is a low-affinity N-methyl-D-aspartate receptor inhibitor. There is evidence that these agents modulate some of the pathways involved in I/R physiopathology. Intestinal I/R was induced in rats by clamping the superior mesenteric artery for 60 minutes, followed by 60 minutes of reperfusion. Rats either received saline or the drugs studied. At the end of the procedure, serum concentrations of tumor necrosis factor-alpha (TNF-alpha), malonaldehyde (MDA), and total antioxidant capacity (TAC) were determined and intestinal morphology analyzed. I/R resulted in tissue damage, serum TNF-alpha and MDA elevations, and depletion of TAC. All drugs showed tissue protection. Only triflusal reduced TNF-alpha levels. All drugs lowered MDA levels, but only triflusal and S-adenosylmethionine maintained the serum TAC.
缺血/再灌注(I/R)是一种引发强烈炎症反应的病症。目前尚无理想的治疗方法。曲氟柳是一种具有抗炎作用的抗血小板水杨酸衍生物。S-腺苷甲硫氨酸是谷胱甘肽(一种内源性抗氧化剂)的代谢前体。右美沙芬是一种低亲和力的N-甲基-D-天冬氨酸受体抑制剂。有证据表明,这些药物可调节I/R病理生理学中涉及的一些途径。通过夹闭大鼠肠系膜上动脉60分钟,然后再灌注60分钟来诱导肠I/R。大鼠分别接受生理盐水或所研究的药物。在实验结束时,测定血清肿瘤坏死因子-α(TNF-α)、丙二醛(MDA)和总抗氧化能力(TAC)的浓度,并分析肠道形态。I/R导致组织损伤、血清TNF-α和MDA升高以及TAC耗竭。所有药物均显示出组织保护作用。只有曲氟柳降低了TNF-α水平。所有药物均降低了MDA水平,但只有曲氟柳和S-腺苷甲硫氨酸维持了血清TAC。