Literature DB >> 26884941

The protective effects of total phenols in magnolia officinalix rehd. et wils on gastrointestinal tract dysmotility is mainly based on its influence on interstitial cells of cajal.

Hui Tian1, Dazhi Huang2, Tao Li3, Lihua Huang2, Xingguang Zheng2, Danxia Tang2, Lu Zhang2, Jian Wang2.   

Abstract

Magnolia officinalix Rehd. et Wils is a kind of herb which is widely used for gastrointestinal tract mobility disorder in Asian countries. In this study, we investigated whether the total phenols of Magnolia officinalix Rehd. et Wils (TPM) treatment improves gastrointestinal tract dysmobility induced by intraperitoneal injection of atropine (5 mg/kg) in rats. Rats were randomly grouped into three units: TPM-pretreated/atropine-treated group, atropinetreated group and control group. TPM were administrated for 7 days. Gastric residual rate and intestinal transit were measured 20 min after atropine injected, and gastrointestinal hormones (including: gastrin (GAS), motilin (MTL), somatostatin (SS) and p substance (PS) levels in serum were also measured by ELISA kits. The number and distribution of interstitial cells of Cajal (ICCs) in stomach were detected by immunohistochemistry analysis, while c-kit and stem cell factor (SCF) expressions in stomach were also measured by western blotting. We found that TPM pretreatment significantly improved atropine-induced gastric residual rate increase, while had no significantly effects on intestinal transit; it also significantly normalized GAS, MTL and PS serum levels. Atropine-induced ICCs numbers decreased in both sinuses ventriculi and body of stomach, which is improved by TPM pretreatment. Western blotting results showed the expressions of c-kit and SCF were down-regulated after atropine injection, which can be reversed with TPM pretreatment. These results above indicates that TPM treatment can significantly protected atropine-induced gastric dysmoblility, which may owed to its regulation on c-kit/SCF signing pathway.

Entities:  

Keywords:  Magnolia officinalix Rehd. et Wils; gastrointestinal tract; interstitial cells of Cajal (ICCs); mobility disorder

Year:  2015        PMID: 26884941      PMCID: PMC4723786     

Source DB:  PubMed          Journal:  Int J Clin Exp Med        ISSN: 1940-5901


  23 in total

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Journal:  Ann N Y Acad Sci       Date:  2006-11       Impact factor: 5.691

Review 6.  Signaling by Kit protein-tyrosine kinase--the stem cell factor receptor.

Authors:  Robert Roskoski
Journal:  Biochem Biophys Res Commun       Date:  2005-11-11       Impact factor: 3.575

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8.  Impaired development of interstitial cells and intestinal electrical rhythmicity in steel mutants.

Authors:  S M Ward; A J Burns; S Torihashi; S C Harney; K M Sanders
Journal:  Am J Physiol       Date:  1995-12

9.  Interstitial cells of Cajal in abdominal sepsis and hypertension-induced ileus in rats.

Authors:  Zheng Lou; Jie Shou Li
Journal:  Eur Surg Res       Date:  2009-05-13       Impact factor: 1.745

10.  Subtotal nephrectomy inhibits the gastric emptying of liquid in awake rats.

Authors:  José Ronaldo Vasconcelos da Graça; Cynara Carvalho Parente; Robério Ferreira Fiúza; Pedro Alberto Freitas da Silva; Bruno Teixeira Mota; Luiz Derwal Salles; Camila Meirelles de Souza Silva; Moisés Tolentino Bento da Silva; Ricardo Brandt de Oliveira; Armenio Aguiar Dos Santos
Journal:  Physiol Rep       Date:  2015-02-12
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Review 3.  Interstitial Cells of Cajal: Potential Targets for Functional Dyspepsia Treatment Using Medicinal Natural Products.

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Journal:  Evid Based Complement Alternat Med       Date:  2021-06-30       Impact factor: 2.629

  3 in total

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