Nurullahoglu-Atalik K E, Okudan N, Belviranli M, Gokbel H, Oz M, Esen H
Department of Pharmacology, Selcuk University, Konya, Turkey.
Bratisl Lek Listy. 2012;113(8):465-70. doi: 10.4149/bll_2012_103.
Curcumin is an antioxidant molecule that has been shown to attenuate ischemia/reperfusion (I/R) injury in several organ systems. In the present study, we aimed to evaluate the possible effects of curcumin on contractile response to agonists and histopathological alterations in rat esophagus subjected to mesenteric I/R.
Adult male Wistar albino rats were randomly allocated to 4 groups, namely group I: sham-operated animals (n=10); group II: animals subdued to I/R injury only (n=10) and laparotomy; 45 minutes of superior mesenteric artery ligation were followed by 2 hours of reperfusion, group III: curcumin/sham (n=10); 20 days before I/R, curcumin (200 mg/kg/) was administered by gastric gavage, and group IV: curcumin-I/R (n=10). Mesenteric ischemia/reperfusion model was generated by clamping the superior mesenteric artery for 45 min followed by reperfusion for 2 h. Oral administration of curcumin by gavage at a dose of 200 mg/kg/day lasted 20 days just before inducing the mesenteric ischemia. At the end of reperfusion period, all animals were sacrificed and esophagus samples were collected to assess the contractile response to agonists and histopathological alterations.
Ischemia/reperfusion significantly decreased the contractile responses to carbachol and KCl and this decrease was attenuated by curcumin. Pretreatment with curcumin caused a remarkable decrease in histopathological parameters such as edema, congestion and inflammatory cells.
The results of the present study demonstrate for the first time that curcumin can attenuate the esophageal injury associated with I/R (Tab. 4, Fig. 3, Ref. 32).
姜黄素是一种抗氧化分子,已被证明可减轻多个器官系统的缺血/再灌注(I/R)损伤。在本研究中,我们旨在评估姜黄素对肠系膜I/R大鼠食管对激动剂的收缩反应和组织病理学改变的可能影响。
成年雄性Wistar白化大鼠随机分为4组,即I组:假手术动物(n = 10);II组:仅遭受I/R损伤(n = 10)并进行剖腹手术;肠系膜上动脉结扎45分钟,随后再灌注2小时,III组:姜黄素/假手术组(n = 10);在I/R前20天,通过胃管给予姜黄素(200 mg/kg/),IV组:姜黄素-I/R组(n = 10)。通过夹闭肠系膜上动脉45分钟,随后再灌注2小时建立肠系膜缺血/再灌注模型。在诱导肠系膜缺血前,以200 mg/kg/天的剂量通过胃管口服姜黄素,持续20天。在再灌注期结束时,处死所有动物并收集食管样本,以评估对激动剂的收缩反应和组织病理学改变。
缺血/再灌注显著降低了对卡巴胆碱和氯化钾的收缩反应,而姜黄素减轻了这种降低。姜黄素预处理导致组织病理学参数如水肿、充血和炎症细胞显著减少。
本研究结果首次证明姜黄素可减轻与I/R相关的食管损伤(表4,图3,参考文献32)。