Zhao Yin-pan, Tang Xu-dong, Bian Zhao-xiang, Wang Feng-yun, Yang Jian-qin, Su Min, Wang Wei
Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing (100091), China.
School of Chinese Medicine of Hong Kong Baptist University, China.
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2013 Nov;33(11):1507-14.
To establish a new disease-syndrome-symptom integrated diarrhea-predominant irritable bowel syndrome (IBS-D) rat model of Gan stagnation and Pi deficiency syndrome (GSPDS).
(1) The model establishment method: We combined mother-infant separation, chronic restraint, and senna gavage to establish a new IBS-D model of GSPDS. Totally 48 experimental rats were divided into the normal group (Group A), the mother-infant separation group (Group B), the chronic restraint group (Group C), and the senna gavage group (Group D), the mother-infant separation + senna gavage group (Group E), and the mother-infant separation + chronic restraint + senna gavage group (Group F), 8 in each group. (2) The model evaluation method: We used pain threshold indicating colorectal distension to represent for the visceral sensitivity, thus evaluating the establishment of "disease" model; open field test and serum D-xylose levels to evaluate the establishment of GSPDS model; defecation numbers of grain and loose stool rate to evaluate the establishment of diarrhea symptom.
(1) Compared with Group A, the body weight gained less in Group F, showing statistical difference (P < 0.05). (2) The pain threshold significantly decreased in Group F, showing statistical difference when compared with Group A (P < 0.05). (3) Compared with Group A, the total cross number, the standing number, and the decoration number in Group F significantly decreased (P < 0.05). (4) Compared with Group A, the serum D-xylose level of Group F significantly decreased (P < 0.05). (5) Compared with Group A, the defecation numbers of grain and the loose stool rate significantly increased, showing statistical difference (P < 0.05).
A new disease-syndrome-symptom integrated IBS-D animal model of GSPDS successfully established might be a better animal model used for studying IBS by Chinese medicine. However, further studies are needed.
建立一种新的肝郁脾虚证腹泻型肠易激综合征(IBS-D)病证结合大鼠模型。
(1)模型建立方法:采用母婴分离、慢性束缚和番泻叶灌胃相结合的方法建立新的肝郁脾虚证IBS-D模型。将48只实验大鼠分为正常组(A组)、母婴分离组(B组)、慢性束缚组(C组)、番泻叶灌胃组(D组)、母婴分离+番泻叶灌胃组(E组)、母婴分离+慢性束缚+番泻叶灌胃组(F组),每组8只。(2)模型评价方法:采用结直肠扩张疼痛阈值代表内脏敏感性,评价“疾病”模型的建立;采用旷场试验和血清D-木糖水平评价肝郁脾虚证模型的建立;采用排粒数和稀便率评价腹泻症状的建立。
(1)与A组比较,F组体重增加较少,差异有统计学意义(P<0.05)。(2)F组疼痛阈值显著降低,与A组比较差异有统计学意义(P<0.05)。(3)与A组比较,F组总穿越次数、站立次数和修饰次数显著减少(P<0.05)。(4)与A组比较,F组血清D-木糖水平显著降低(P<0.05)。(5)与A组比较,F组排粒数和稀便率显著增加,差异有统计学意义(P<0.05)。
成功建立的一种新的肝郁脾虚证腹泻型肠易激综合征病证结合动物模型可能是用于中医研究肠易激综合征的较好动物模型。然而,仍需进一步研究。