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Establishment of Mouse Models of Psoriasis with Blood Stasis Syndrome Complicated with Glucose and Lipid Metabolism Disorders

机译:用血瘀综合征复杂化血糖和脂质代谢障碍的牛皮癣小鼠模型的建立

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Background. Psoriasis has been reported as a high-risk factor for quality of life and survival rate in patients with metabolic disorder. However, there is no animal model for studying this disease. This study aimed to establish and evaluate mouse models of psoriasis with blood stasis syndrome (which is a key to psoriasis pathogenesis, according to Chinese Medicine) complicated with metabolic disorders. Method. Forty-five C57BL/6 mice were randomly divided into the blank control (Control), psoriasis (Imiquimod (IMQ)), psoriasis with metabolic disorders (IMQ?+?streptozotocin (STZ)), psoriasis with blood stasis syndrome (BSS) (IMQ?+?BSS), and psoriasis with blood stasis syndrome complicated with metabolic disorders (IMQ?+?STZ?+?BSS) groups (n?=?9 mice/group). Psoriasis lesions were induced using IMQ cream (on both the ears and back, except in the Control group). Mice of the IMQ?+?BSS group were fed a half-fat, high-sugar diet and stimulated with ice-water swimming every day. Mice of the IMQ?+?STZ group were fed a half-fat, high-sugar diet and injected with STZ. Mice of the IMQ?+?STZ?+?BSS group were subjected to the same treatments as the IMQ?+?STZ and IMQ?+?BSS groups. After induction, the mice in each group were observed for vital signs, ear thickness, body weight, and psoriasis area and severity index (PASI) score. The mice were fasted for 12?h before determination of related laboratory serum indexes. Dorsal skin lesions, aortic arch pathology sections, and signal transducer and activator of transcription 3 (STAT3) were examined by H&E staining and immunohistochemistry. Results. Laboratory indexes in the four model groups were significantly different from those in the Control group (p0.01); indicators of the IMQ?+?STZ, IMQ?+?BSS, and IMQ?+?STZ?+?BSS groups showed varying degrees of difference from those of the IMQ group. Conclusions. The established mouse models of psoriasis blood stasis syndrome complicated with glucose and lipid metabolism disorders met the clinical and Chinese Medicine characteristics, and thus they could be used as animal models in future studies of psoriasis complicated with glucose and lipid metabolism disorders.
机译:背景。牛皮癣已被报告为代谢障碍患者生命质量和生存率的高危因素。然而,没有动物模型用于研究这种疾病。本研究旨在建立和评估血瘀综合征的牛皮癣的小鼠模型(这是牛皮癣发病机制的关键,根据中药复杂于代谢障碍。方法。将四十五个C57BL / 6小鼠随机分为空白控制(对照),牛皮癣(Imimimod(IMQ)),具有代谢紊乱的牛皮癣(IMQ?+α+β-链脲佐菌素(STZ)),牛皮癣血瘀综合征(BSS)( IMQ?+?BSS),血瘀综合征与代谢紊乱(IMQ?+?STZ?+?BSS)组成(n?= 9只小鼠/组)的牛皮癣。使用IMQ霜诱导牛皮癣病变(在耳朵和背部,除了对照组外)。 IMQ?+ BSS组的小鼠喂养半脂肪,高糖饮食,并每天用冰水游泳刺激。 IMQ的小鼠+ + STZ组喂养半脂肪,高糖饮食并注射STZ。 IMQ?+ + + + + + BSS组的小鼠作为IMQ?+?STZ和IMQ?+?BSS组的相同治疗。诱导后,观察到每组小鼠用于生命体征,耳厚度,体重和牛皮癣面积和严重程度指数(PASI)得分。在测定相关实验室血清指数之前,小鼠禁食12℃。通过H&E染色和免疫组化检查转录3(STAT3)的背部皮肤病膜,主动脉弓病理学切片和信号传感器和信号传感器和激活剂。结果。四种模型组中的实验室指标与对照组中的那些有显着不同(P <0.01); IMQ的指标?+?STZ,IMQ?+?BSS和IMQ?STZ?+?BSS组显示与IMQ组的不同程度。结论。与葡萄糖和脂质代谢紊乱的牛皮癣血瘀综合征的既定小鼠模型都符合临床和中药特征,因此它们可以用作未来牛皮癣和血脂代谢障碍的牛皮癣研究的动物模型。

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