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苓桂术甘汤联合热量限摄对湿疹模型大鼠皮损的影响及其机制分析 被引量:10

Effect of Calorie-restriction Therapy Combined Linggui Zhugan Decoction on Eczema Model Rats
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摘要 目的探讨苓桂术甘汤联合热量限摄对湿疹模型大鼠的疗效观察及其机制分析。方法 50只Wistar大鼠随机分为正常组(A组)、模型组(B组)、泼尼松组(C组)、限摄组(D组)、中药限摄组(E组)。除A组外,各组大鼠均予2,4-二硝基氯苯(DNCB)造模建立湿疹大鼠模型。各组均在实验造模成功后第2天灌胃给药,A、B组每天给予0.9%氯化钠注射液20 mL/kg,继续原饲料喂养3天;C组每天给予泼尼松片25 mg/kg,溶于0.9%氯化钠注射液20 mL/d灌胃;D组给予0.9%氯化钠注射液20 mL/kg,并热量限摄3天,不限饮水;E组每天给予苓桂术甘汤2 mL/kg,并热量限摄3天,不限饮水。观察造模前后及干预后各组大鼠体重变化和一般情况,湿疹皮损评分和疗效情况,检测各组IL-4、γ-干扰素(IFN-γ)水平变化和肠道黏膜分泌型免疫球蛋白A (SIgA)分泌情况。结果与造模前比较,造模后各组大鼠体重正常性升高,干预后D、E组较A、B、C组下降(P<0.05)。热量限摄4天后,与B组比较,C、D、E组大鼠皮损评分明显降低,疗效指数升高(P<0.01);C、D、E组右耳肿胀度明显减少(P<0.01)。与C组比较,E组大鼠右耳肿胀度明显增加(P<0.05),抑制率降低(P<0.05);与B组比较,C组IFN-γ值明显升高(P<0.05),SIgA水平明显下降(P<0.05);E组IL-4值较B组明显升高(P<0.05),SIgA水平明显下降(P<0.05);D组SIgA水平明显降低(P<0.05),但D、E两组比较,差异无统计学意义(P>0.05)。结论热量限摄可以明显改善湿疹大鼠皮损评分及湿疹皮肤肿胀程度,加用苓桂术甘汤后亦有效,尚不能确定是通过调节机免疫平衡或改善其肠道免疫状态而达到,其具体作用机制尚需进一步研究。 Objective To observe the effects of caloric restriction combined Linggui Zhugan Decoction(LGZGD) on eczema rats and to analyze its mechanism. Methods Totally 50 Wistar rats were randomly divided into normal group(Group A), saline group(Group B), bonisone group(Group C), caloric restriction group(Group D), and TCM caloric restriction group(Group E). Except Group A, rats in the rest groups were modeled by 2,4-dinitrochlorobenzene(DNCB) to establish eczema rat model. Rats were administered by corresponding drugs by gastrogavage on the 2 nd day of successful modeling. Rats in Group A and B were given 0.9% sodium chloride injection at 2 mL/kg, and fed with former forage for 3 successive days. Rats in Group C were given prednisone tablet at 25 mg/kg by dissolving in 0.9% sodium chloride injection(20 mL/d). Rats in Group D were given 0.9% sodium chloride injection(20 mL/kg) and limit calorie for 3 days(free to drink water). Rats in Group E were given LGZGD 2 mL/kg and limit calorie for 3 days(free to drink water). After treatment the right ear skin lesions and swelling were observed to evaluate the efficacy. Changes of IL-4, interferon-γ(IFN-γ), and secretory IgA(SIgA) were also observed. Results Compared with before modeling, body weight increased to normal levels in each group after modeling. They decreased more in Group D and E than in Group A/B/C(P<0.05). After 4 days of caloric restriction, as compared with Group B, the lesion scores of rats in Group C, D, and E were significantly lower, and the curative effect was significantly improved(P<0.01);the swelling degree of right ear was significantly lessened(P<0.01). Compared with Group C, the swelling degree of right ear was significantly increased in Group E(P<0.05),and the inhibition rate was lowered(P<0.05). The IFN-γ value was significantly higher in Group C than in Group B(P<0.05). The SIgA level was significantly lower in Group C than in Group B(P<0.05). IL-4 value was significantly higher in Group E than in Group B(P<0.05). SIgA level was significantly lower in Group E than in Group B(P<0.05). SIgA level was significantly decreased in Group D, but with no significant difference between Group D and E(P>0.05). Conclusions Caloric restriction significantly improved the skin lesions and eczema skin swelling of eczema rats. Combined with LGZGD was also effective, but whether it was achieved by regulating the immune balance of the body or improving intestinal immunity. The specific mechanisms needs further studies.
作者 汪园园 金明华 黄颖娟 张丽娜 姜金鹏 秦鉴 WANG Yuan-yuan;JIN Ming-hua;HUANG Ying-juan;ZHANG Li-na;JIANG Jin-peng;QIN Jian(Department of Chinese Medicine,The East Division of First Affiliated Hospital,Sun Yat-Sen University,Guangzhou,510700;Department of Traditional Chinese Medicine,First Affiliated Hospital,Sun Yat-Sen University,Guangzhou,510080;Department of Traditional Chinese Medicine,Sixth Affiliated Hospital,Sun Yat-Sen University,Guangzhou,510000)
出处 《中国中西医结合杂志》 CAS CSCD 北大核心 2020年第4期465-469,共5页 Chinese Journal of Integrated Traditional and Western Medicine
基金 广州市黄埔区科技计划项目(No.20132905)。
关键词 苓桂术甘汤 热量限摄疗法 湿疹 白介素-4 γ-干扰素 肠道黏膜分泌型免疫球蛋白A Linggui Zhugan Decoction caloric restriction therapy eczema interferon-γ IL-4 secretory IgA
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