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Effects of indomethacin, celecoxib and meloxicam on glutathione, malondialdehyde and myeloperoxidase in rat gastric tissue

机译:消炎痛,塞来昔布和美洛昔康对大鼠胃组织中谷胱甘肽,丙二醛和髓过氧化物酶的影响

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In the present study, we examined the effects of indomethacin, celecoxib and meloxicam on the stomach and on levels of glutathione (GSH), malondialdehyde (MDA) and activity of myeloperoxidase (MPO) in gastric tissues of rats. The ulcer area was 31.1 ± 10.7 mm2 in indomethacin-treated rats (20 mg kg-1) and 17.3 ± 38 mm2 in meloxicam-treated rats (7.5 mg kg-1). Celecoxib, at a dose of 100 mg kg-1, did not cause any damage in the rat gastric tissue. GSH levels were 1.6 ± 0.3, 6 ± 0.7 and 3.3 ± 0.4 nmol/g protein in the indomethacin-, celecoxib- and meloxicam-treated groups, respectively. MPO activities were 27.6 ± 2.4, 12.3 ± 1.5 and 14.9 ± 0.7 U/g protein in the indomethacin-, celecoxib- and meloxicam-treated rats, respectively. MDA levels were 184.8 ± 40.9, 81.47 ± 15.4, 113 ± 18.1 mol/g protein, respectively. In the control group, GSH, MDA levels and activity of MPO were 6.5 ± 1 nmol/g protein, 62.1 ± 11.1 mol/g protein, 11.2 ± 1.5 U/g protein, respectively.Taking these data into consideration, we propose that the depletion of GSH in gastric mucosa, as well as inhibition of PG synthesis, may play an important role in development of gastric mucosal injury. In addition, there is a parallelism between the increase of MPO activity, levels of MDA and severity of gastric mucosal injury.
机译:在本研究中,我们检查了吲哚美辛,塞来昔布和美洛昔康对胃以及大鼠胃组织中谷胱甘肽(GSH),丙二醛(MDA)和髓过氧化物酶(MPO)活性的影响。吲哚美辛治疗的大鼠(20 mg kg -1 )的溃疡面积为31.1±10.7 mm 2 ,美洛昔康的溃疡面积为17.3±38 mm 2 治疗的大鼠(7.5 mg kg -1 )。塞来昔布的剂量为100 mg kg -1 ,对大鼠胃组织未造成任何损害。吲哚美辛,塞来昔布和美洛昔康治疗组的GSH水平分别为1.6±0.3、6±0.7和3.3±0.4 nmol / g蛋白。在吲哚美辛,塞来昔布和美洛昔康治疗的大鼠中,MPO活性分别为27.6±2.4、12.3±1.5和14.9±0.7 U / g蛋白。 MDA水平分别为184.8±40.9、81.47±15.4、113±18.1 mol / g蛋白质。对照组的GSH,MDA和MPO活性分别为6.5±1 nmol / g蛋白,62.1±11.1 mol / g蛋白,11.2±1.5 U / g蛋白。胃粘膜中GSH的耗竭以及PG合成的抑制可能在胃粘膜损伤的发展中起重要作用。另外,MPO活性的增加,MDA水平和胃粘膜损伤的严重程度之间存在平行关系。

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