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Herbal prescription Chang'an II repairs intestinal mucosal barrier in rats with post-inflammation irritable bowel syndrome.
Wang, Feng-yun; Su, Min; Zheng, Yong-qiu; Wang, Xiao-ge; Kang, Nan; Chen, Ting; Zhu, En-lin; Bian, Zhao-xiang; Tang, Xu-dong.
Afiliación
  • Wang FY; Gastroenterology Department, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
  • Su M; Xuanwu Traditional Chinese Medical Hospital, Beijing 100000, China.
  • Zheng YQ; Research Center, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
  • Wang XG; Gastroenterology Department, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
  • Kang N; Gastroenterology Department, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
  • Chen T; Gastroenterology Department, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
  • Zhu EL; Gastroenterology Department, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
  • Bian ZX; School of Chinese Medicine, Hong Kong Baptist University, Kowloon Tong, China.
  • Tang XD; Gastroenterology Department, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
Acta Pharmacol Sin ; 36(6): 708-15, 2015 Jun.
Article en En | MEDLINE | ID: mdl-25960135
AIM: The herbal prescription Chang'an II is derived from a classical TCM formula Tong-Xie-Yao-Fang for the treatment of liver-qi stagnation and spleen deficiency syndrome of irritable bowel syndrome (IBS). In this study we investigated the effects of Chang'an II on the intestinal mucosal immune barrier in a rat post-inflammation IBS (PI-IBS) model. METHODS: A rat model of PI-IBS was established using a multi-stimulation paradigm including early postnatal sibling deprivation, bondage and intrarectal administration of TNBS. Four weeks after TNBS administration, the rats were treated with Chang'an II (2.85, 5.71 and 11.42 g · kg(-1) · d(-1), ig) for 14 d. Intestinal sensitivity was assessed based on the abdominal withdrawal reflex (AWR) scores and fecal water content. Open field test and two-bottle sucrose intake test were used to evaluate the behavioral changes. CD4(+) and CD8(+) cells were counted and IL-1ß and IL-4 levels were measured in intestinal mucosa. Transmission electron microscopy was used to evaluate ultrastructural changes of the intestinal mucosal barrier. RESULTS: PI-IBS model rats showed significantly increased AWR reactivity and fecal water content, and decreased locomotor activity and sucrose intake. Chang'an II treatment not only reduced AWR reactivity and fecal water content, but also suppressed the anxiety and depressive behaviors. Ultrastructural study revealed that the gut mucosal barrier function was severely damaged in PI-IBS model rats, whereas Chang'an II treatment relieved intestinal mucosal inflammation and repaired the gut mucosal barrier. Furthermore, PI-IBS model rats showed a significantly reduced CD4(+)/CD8(+) cell ratio in lamina propria and submucosa, and increased IL-1ß and reduced IL-4 expression in intestinal mucosa, whereas Chang'an II treatment reversed PI-IBS-induced changes in CD4(+)/CD8(+) cell ratio and expression of IL-1ß and IL-4. CONCLUSION: Chang'an II treatment protects the intestinal mucosa against PI-IBS through anti-inflammatory, immunomodulatory and anti-anxiety effects.
Asunto(s)
Antiinflamatorios/farmacología; Colitis/tratamiento farmacológico; Colon/efectos de los fármacos; Medicamentos Herbarios Chinos/farmacología; Fármacos Gastrointestinales/farmacología; Mucosa Intestinal/efectos de los fármacos; Síndrome del Colon Irritable/tratamiento farmacológico; Cicatrización de Heridas/efectos de los fármacos; Animales; Animales Recién Nacidos; Conducta Animal/efectos de los fármacos; Linfocitos T CD4-Positivos/efectos de los fármacos; Linfocitos T CD4-Positivos/inmunología; Linfocitos T CD4-Positivos/metabolismo; Linfocitos T CD8-positivos/efectos de los fármacos; Linfocitos T CD8-positivos/inmunología; Linfocitos T CD8-positivos/metabolismo; Colitis/inducido químicamente; Colitis/inmunología; Colitis/metabolismo; Colitis/patología; Colitis/psicología; Colon/inmunología; Colon/metabolismo; Colon/ultraestructura; Modelos Animales de Enfermedad; Combinación de Medicamentos; Heces/química; Conducta Alimentaria/efectos de los fármacos; Preferencias Alimentarias/efectos de los fármacos; Inmunidad Mucosa/efectos de los fármacos; Mediadores de Inflamación/metabolismo; Interleucina-1beta/metabolismo; Interleucina-4/metabolismo; Mucosa Intestinal/inmunología; Mucosa Intestinal/metabolismo; Mucosa Intestinal/ultraestructura; Síndrome del Colon Irritable/inducido químicamente; Síndrome del Colon Irritable/inmunología; Síndrome del Colon Irritable/metabolismo; Síndrome del Colon Irritable/patología; Síndrome del Colon Irritable/psicología; Masculino; Medicina Tradicional China; Actividad Motora/efectos de los fármacos; Umbral del Dolor/efectos de los fármacos; Ratas Sprague-Dawley; Ácido Trinitrobencenosulfónico

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cicatrización de Heridas / Fármacos Gastrointestinales / Medicamentos Herbarios Chinos / Colitis / Colon / Síndrome del Colon Irritable / Mucosa Intestinal / Antiinflamatorios Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Acta Pharmacol Sin Asunto de la revista: FARMACOLOGIA Año: 2015 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cicatrización de Heridas / Fármacos Gastrointestinales / Medicamentos Herbarios Chinos / Colitis / Colon / Síndrome del Colon Irritable / Mucosa Intestinal / Antiinflamatorios Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Acta Pharmacol Sin Asunto de la revista: FARMACOLOGIA Año: 2015 Tipo del documento: Article