Vivatvakin Sarocha, Werawatganon Duangporn, Somanawat Kanjana, Klaikeaw Naruemon, Siriviriyakul Prasong
Department of Physiology, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
Department of Pathology, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
Pharmacogn Mag. 2017 Jul;13(Suppl 2):S306-S310. doi: 10.4103/pm.pm_502_16. Epub 2017 Jul 11.
To investigates the mucoprotective effect of genistein on gastric injury in rats with indomethacin (IMN)-induced gastropathy.
Male Sprague-Dawley rats were randomly divided into three groups. Group 1 (control; = 6) was given distilled water (DW). Group 2 (IMN; = 6) was given indomethacin (IMN) 150 mg/kg dissolved in 5% sodium bicarbonate (NaHCO) 1 mL/rat via intragastric tube at time 0 and 4 h. Group 3 (genistein; = 6) was given genistein 100 mg/kg dissolved in 0.1% dimethyl sulfoxide (DMSO) plus IMN 150 mg/kg at time described as group 2. Four hours after the second dose, the stomach was removed to examine iNOS western blot expression, malondialdehyde (MDA), and histopathologic examination. Serum was collected to determine TNF-alpha and prostaglandin E (PGE) levels using ELISA technique.
Tissue MDA and serum TNF-alpha were significantly increased in the IMN group, as compared to the control group (9.70 ± 0.40 . 1.56 ± 0.14 nmol/mg protein, = 0.000; 210.28 ± 0.98 . 126.4 ± 0.13 pg/mL, = 0.000, respectively) and decreased in the genistein group when compared to the IMN group (2.87 ± 0.37 . 9.70 ± 0.40 nmol/mg protein, = 0.000; 156.59 ± 0.10 . 210.28 ± 0.98 pg/mL, = 0.000, respectively). Serum PGE level in IMN group was decreased significantly compared with control group (152.83 ± 0.10 . 303.33 ± 2.16 pg/mL, = 0.000) and increased in the genistein group compared to the IMN group (247.65 ± 0.01 . 152.83 ± 0.10 pg/mL, = 0.000). Expression of tissue iNOS was increased in the IMN group and improved in genistein groups. Most of the rats in the IMN group developed moderate to severe gastric erosion and ulcers. Gastric erosions and neutrophil infiltration score were significantly decreased in the genistein group.
Genistein attenuated IMN-induced gastropathy in rats by reducing inflammation, decreasing oxidative stress, restoring mucoprotective function, and improving gastric histopathology.
This is an experimental study of the effect of NSAIDs in gastropathy. This study demonstrated the efficacy of genistein in treatment of NSAIDs-induced gastropathy. Genistein efficacy is reflected in the attenuation of histological alterations, with improvement in key biological parameters involved in the pathogenesis of NSAIDs gastropathy. NSAIDs: Non-steroidal anti-inflammatory drugs; IMN: Indomethacin; COX: Cyclooxygenase; TNF: Tumor necrosis factor; ICAM: Intercellular adhesion molecule; iNOS: Inducible nitric oxide synthase; MDA: Malondialdehyde; CINC: Cytokine-induced neutrophil chemoattractant.
研究染料木黄酮对吲哚美辛(IMN)诱导的大鼠胃病胃损伤的黏膜保护作用。
雄性Sprague-Dawley大鼠随机分为三组。第1组(对照组;n = 6)给予蒸馏水(DW)。第2组(IMN组;n = 6)在0时和4小时经胃管给予溶解于1 mL/大鼠5%碳酸氢钠(NaHCO)中的吲哚美辛(IMN)150 mg/kg。第3组(染料木黄酮组;n = 6)在与第2组相同时间给予溶解于0.1%二甲基亚砜(DMSO)中的染料木黄酮100 mg/kg加IMN 150 mg/kg。第二次给药后4小时,取出胃进行诱导型一氧化氮合酶(iNOS)蛋白免疫印迹表达、丙二醛(MDA)检测及组织病理学检查。收集血清,采用酶联免疫吸附测定(ELISA)技术测定肿瘤坏死因子-α(TNF-α)和前列腺素E(PGE)水平。
与对照组相比,IMN组组织MDA和血清TNF-α显著升高(分别为9.70±0.40 μmol/mg蛋白,P = 0.000;210.28±0.98 pg/mL,P = 0.000),与IMN组相比,染料木黄酮组降低(分别为2.87±0.37 μmol/mg蛋白,P = 0.000;156.59±0.10 pg/mL,P = 0.000)。IMN组血清PGE水平与对照组相比显著降低(152.83±0.10 pg/mL,P = 0.000),与IMN组相比,染料木黄酮组升高(247.65±0.01 pg/mL,P = 0.000)。IMN组组织iNOS表达增加,染料木黄酮组改善。IMN组大多数大鼠出现中度至重度胃糜烂和溃疡。染料木黄酮组胃糜烂和中性粒细胞浸润评分显著降低。
染料木黄酮通过减轻炎症、降低氧化应激、恢复黏膜保护功能和改善胃组织病理学减轻IMN诱导的大鼠胃病。
这是一项关于非甾体抗炎药对胃病影响的实验研究。本研究证明了染料木黄酮治疗非甾体抗炎药诱导的胃病疗效。染料木黄酮的疗效体现在组织学改变的减轻,以及非甾体抗炎药胃病发病机制中关键生物学参数的改善。非甾体抗炎药:NSAIDs;吲哚美辛:IMN;环氧化酶:COX;肿瘤坏死因子:TNF;细胞间黏附分子:ICAM;诱导型一氧化氮合酶:iNOS;丙二醛:MDA;细胞因子诱导的中性粒细胞趋化因子:CINC