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纸质出版日期:2014
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林传权, 陈娟, 李茹柳, 等. 胃乃安新制剂对碘代乙酰胺致慢性浅表性胃炎的干预作用[J]. 中国实验方剂学杂志, 2014,20(19):146-150.
LIN Chuan-quan, CHEN Juan, LI Ru-liu, et al. Effects of New Weinaian Preparation on Chronic Superficial Gastritis Induced by Iodoacetamide[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(19): 146-150.
林传权, 陈娟, 李茹柳, 等. 胃乃安新制剂对碘代乙酰胺致慢性浅表性胃炎的干预作用[J]. 中国实验方剂学杂志, 2014,20(19):146-150. DOI: 10.13422/j.cnki.syfjx.2014190146.
LIN Chuan-quan, CHEN Juan, LI Ru-liu, et al. Effects of New Weinaian Preparation on Chronic Superficial Gastritis Induced by Iodoacetamide[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(19): 146-150. DOI: 10.13422/j.cnki.syfjx.2014190146.
目的:观察胃乃安新制剂对慢性浅表性胃炎的作用。方法:SD大鼠按随机数字表分为正常组(10只)、模型组、胃乃安新制剂高、中、低剂量(9.10,2.87,0.91 g·kg-1)组和胃乃安胶囊(9.10 g·kg-1)组(每组各15只),予模型组及各给药组大鼠自由饮用0.1%碘代乙酰胺3周构建慢性浅表性胃炎模型的同时,各给药组予相应药物干预,模型组和正常对照组予等量自来水灌胃;3周后取胃组织从肉眼观察、病理切片、透射电镜3个层面评价胃乃安新制剂抗碘代乙酰胺致胃黏膜损伤作用,并检测胃组织的丙二醛(MDA)、超氧化物歧化酶(SOD)水平以探讨其可能的作用机制。结果:正常组胃组织未见明显损伤,未见明显炎细胞浸润;与正常组比较,模型组胃组织肉眼可见明显充血水肿,甚至糜烂,镜下见大量炎细胞浸润(P<0.01);由肉眼、病理评分结果,胃乃安新制剂高剂量组、胃乃安胶囊组均有抗胃黏膜损伤作用(与模型组比较P<0.01),且新制剂抗溃疡效果呈剂量依赖性关系;透射电镜观察结果表明,新制剂可明显逆转主细胞、壁细胞的超微结构损伤性改变;新制剂可降低胃组织MDA含量,提升SOD活性,可明显降低胃黏膜的自由基水平(与模型组比较,P<0.01)。结论:胃乃安新制剂对碘代乙酰胺所致慢性浅表性胃炎有显著抗损伤作用,可能通过清除胃黏膜自由基水平的途径发挥作用。
Objective: To investigate effect and mechanism of new Weinaian preparation (NWP) on the rat chronic superfical gastritis(CSG) induced by iodoacetamide. Method: SD rats were randomly divided into normal control group(NC
n=10)
CSG group(n=15)
NWP(9.10
2.87
0.91 g·kg-1) groups(n=15
respectively)and Weinaian capsule group (n=15). The CSG rats were induced by 0.1% iodoacetamide for 3 weeks
the drug groups were given by gavage once a day for 3 weeks with appropriate drugs simultaneously
and the nomal contral and CSG groups were given the same amount of water.The effects of NWP on the CSG rats were evaluated by naked eye
pathological section and transmission electron microscope. The action mechanism of Weinaian was studied by detection the level of malondialdehyde(MDA) and superoxide dismutase(SOD) in the rat gastric mucosal. Result: Contrasted with the NC group
there was obvious injury and inflammation cell in the gastric mucosa of the CSG group. The effects of anti-injury were found in the ranitidine and high-dose group of Weinaian groups (P<0.01)
there was dose-reponse relationship in the three Weinaian groups. The ultrastructure injury of chief and parietal cell were improved by the high-dose group of Weinaian.The group also reduced the level of MDA and increased the activity of SOD in the gastric mucosa(P<0.01
vs CSG group). Conclusion: The new Weinaian preparation can alleviate the gastric mucosal injury of CSG rat induced by iodoacetamide which maybe related to clearing gasrica mucosa radical.
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