首页> 外文期刊>Experimental Eye Research >Combination treatment for allergic conjunctivitis - Plant derived histidine decarboxylase inhibitor and H1 antihistaminic drug
【24h】

Combination treatment for allergic conjunctivitis - Plant derived histidine decarboxylase inhibitor and H1 antihistaminic drug

机译:过敏性结膜炎的联合治疗-植物来源的组氨酸脱羧酶抑制剂和H1抗组胺药

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Aim of present investigation was to study the effect of catechin and the combination of catechin and cetirizine in ovalbumin induced animal model of allergic conjunctivitis. Guinea pigs were divided into 5 groups: normal control, disease control, disease treated with catechin 100 mg/kg, disease treated with cetirizine 10 mg/kg, disease treated with combination of catechin and cetirizine, 50 mg/kg & 5 mg/kg respectively. Sensitization was carried out by intraperitoneal injection of ovalbumin for the period of 14 day. Simultaneously, catechin was administered orally for 14 days while, cetirizine was administered at the day of experiment. Determination of clinical scoring, mast cell and blood histamine content, histidine decarboxylase activity from stomach was carried out. Vascular permeability was measured by dye leakage after secondary challenge of allergen and conjunctival tissues were subjected for histopathological examinations. Treatment with catechin, cetirizine and combination showed significant (P < 0.05) decrease in clinical scoring and vascular permeability. While, catechin 100 mg/kg and catechin 50 mg/kg showed significant (P < 0.05) decrease in histamine content in mast and blood. The treatment also showed significant (P < 0.05) decrease in the histidine decarboxylase enzyme activity. However, cetirizine group did not show any difference in enzyme activity as well as histamine content. Histopathological examination also showed improvement in ulceration and decrease in edema and inflammation in all treatment groups. From the present study, we can conclude that catechin exhibits potent anti-allergic activity by histidine decarboxylase enzyme inhibition and combination shown significant anti-allergic activity at reduced dose by both enzyme inhibition as well as inhibition of histamine receptors. (C) 2015 Elsevier Ltd. All rights reserved.
机译:本研究的目的是研究儿茶素以及儿茶素和西替利嗪的组合在卵清蛋白诱发的过敏性结膜炎动物模型中的作用。豚鼠分为5组:正常对照组,疾病对照,用儿茶素100 mg / kg治疗的疾病,用西替利嗪10 mg / kg治疗的疾病,用儿茶素和西替利嗪联合治疗的疾病50 mg / kg和5 mg / kg分别。通过腹膜内注射卵清蛋白进行敏化14天。同时,儿茶素口服14天,而西替利嗪则在实验当天施用。进行临床评分,肥大细胞和血液中组胺含量,胃中组氨酸脱羧酶活性的测定。继发性变应原激发后,通过染料渗漏测量血管渗透性,并对结膜组织进行组织病理学检查。儿茶素,西替利嗪及其组合治疗显示临床评分和血管通透性显着降低(P <0.05)。而儿茶素100 mg / kg和儿茶素50 mg / kg显示肥大和血液中组胺含量显着降低(P <0.05)。该处理还显示组氨酸脱羧酶活性显着降低(P <0.05)。然而,西替利嗪组在酶活性和组胺含量上没有任何差异。组织病理学检查还显示在所有治疗组中溃疡的改善以及水肿和炎症的减少。从本研究中,我们可以得出结论,儿茶素通过组氨酸脱羧酶的抑制作用表现出强大的抗过敏活性,并且在降低剂量的情况下,通过酶抑制和对组胺受体的抑制作用,组合显示出显着的抗过敏活性。 (C)2015 Elsevier Ltd.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号