Effects of Hemp seed soft capsule on colonic ion transport in rats

AIM To investigate the effect of Hemp seed soft capsule(HSCC) on colonic ion transport and its related mechanisms in constipation rats.METHODS Sprague-Dawley male rats were randomly divided into three groups: normal group, constipation group and HSSC group. Rats in the constipation and HSSC groups w...

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Published inWorld journal of gastroenterology : WJG Vol. 23; no. 42; pp. 7563 - 7571
Main Authors Lu, Xiao-Fang, Jia, Meng-Di, Zhang, Sheng-Sheng, Zhao, Lu-Qing
Format Journal Article
LanguageEnglish
Published United States Baishideng Publishing Group Inc 14.11.2017
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Summary:AIM To investigate the effect of Hemp seed soft capsule(HSCC) on colonic ion transport and its related mechanisms in constipation rats.METHODS Sprague-Dawley male rats were randomly divided into three groups: normal group, constipation group and HSSC group. Rats in the constipation and HSSC groups were administrated loperamide 3 mg/kg per day orally for 12 d to induce the constipation model. Then, the HSSC group was given HSSC 0.126 g/kg per day by gavage for 7 d. The normal and constipation groups were treated with distilled water. After the treatment, the fecal wet weight and water content were measured. The basal short-circuit current(Isc) and resistance were measured by an Ussing Chamber. Besides the in vivo drug delivery experiment above, an in vitro drug application experiment was also conducted. The accumulative concentrations of HSSC(0.1 mg/m L, 0.5 mg/m L, 1.0 mg/m L, 2.5 mg/m L, 5.0 mg/m L, 10.0 mg/m L and 25.0 mg/m L) were added to the normal isolatedcolonic mucosa and the Isc was recorded. Further, after the application of either ion(Cl-or HCO3-) substitution, ion channel-related inhibitor(N-phenylanthranilic acid, glybenclamide, 4,4-diisothiocyano-2,2-stilbenedisulfonic acid or bumetanide) or neural pathway inhibitor [tetrodotoxin(TTX), atropine, or hexamethonium], the Isc induced by HSSC was also measured. RESULTS In the constipation group, the fecal wet weight and the water content were decreased in comparison with the normal group(P < 0.01). After the treatment with HSSC, the fecal wet weight and the water content in the HSSC group were increased, compared with the constipation group(P < 0.01). In the constipation group, the basal Isc was decreased and resistance was increased, in comparison with the normal group(P < 0.01). After the treatment with HSSC, the basal Isc was increased(P < 0.05) and resistance was decreased(P < 0.01) in the HSSC group compared with the constipation group. In the in vitro experiment, beginning with the concentration of 1.0 mg/m L, differences in Isc were found between the experimental mucosa(with HSSC added) and control mucosa. The Isc of experimental mucosa was higher than that of control mucosa under the same concentration(1.0 mg/m L, P < 0.05; 2.5-25 mg/m L, P < 0.01). After the Cl-or HCO3-removal and pretreated with different inhibitors(c AMPdependent and Ca2+-dependent Cl-channels, Na+-K+-2 Cl-cotransporter(NKCC), Na+-HCO3-cotransporter or Cl-/HCO3-exchanger inhibitor), there were differences between experimental mucosa and control mucosa; the Isc of experimental mucosa was lower than that of control mucosa under the same concentration(P < 0.05). Meanwhile, after pretreatment with neural pathway inhibitor(TTX, atropine, or hexamethonium), there were no differences between experimental mucosa and control mucosa under the same concentration(P > 0.05).CONCLUSION HSSC ameliorates constipation by increasing colonic secretion, which is mediated via the coaction of c AMPdependent and Ca2+-dependent Cl-channels, NKCC, Na+-HCO3-cotransporter or Cl-/HCO3-exchanger.
Bibliography:Xiao-Fang Lu;Meng-Di Jia;Sheng-Sheng Zhang;Lu-Qing Zhao;Digestive Disease Center, Beijing Hospital of Traditional Chinese Medicine Affiliated to Capital Medical University
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Author contributions: Lu XF, Zhang SS and Zhao LQ designed the study; Lu XF and Jia MD performed the majority of experiments, analyzed the data and wrote the article; Lu XF and Jia MD contributed equally to this work; All the authors approved the final version of the article to be published.
Telephone: +86-10-52176634 Fax: +86-10-52176634
Supported by the Clinical Medicine Development Project of Beijing Municipal Administration of Hospitals, No. ZYLX201411.
Correspondence to: Sheng-Sheng Zhang, MD, Digestive Disease Center, Beijing Hospital of Traditional Chinese Medicine Affiliated to Capital Medical University, 23 Meishuguanhou Street, Beijing 100010, China. zhss2000@163.com
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v23.i42.7563