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        痛瀉要方對D-IBS結腸黏膜5-HT及CGA相關離子通道轉運機制的研究

        2015-04-02 21:09:19張聲生,楊成
        首都醫(yī)科大學學報 2015年4期
        關鍵詞:離子通道羥色胺結腸

        【摘要】腹瀉型腸易激綜合征(diarrhea-predominant irritable bowel syndrome,D-IBS)是臨床常見的功能性腸道疾病,給患者的生活和工作帶來諸多不便。痛瀉要方作為中醫(yī)古代著名方劑,能夠明顯減輕D-IBS患者的腹痛、腹瀉癥狀,提高其生活和工作質量,但其治療的確切機制尚不明確,本文從5-羥色胺及嗜鉻素A(chromogranin A,CGA)相關離子通道轉運機制的角度出發(fā),探討痛瀉要方對D-IBS結腸黏膜離子通道的影響,以期為后續(xù)的臨床與基礎研究提供可靠的依據(jù)。

        [doi: 10.3969/j.issn.1006-7795.2015.04.026]·轉化醫(yī)學研究·

        基金項目:國家自然科學基金(81473644),北京市醫(yī)院管理局臨床醫(yī)學發(fā)展專項經(jīng)費資助(ZYLX201411),北京市衛(wèi)生系統(tǒng)高層次衛(wèi)生技術人才培養(yǎng)計劃(2011-2-13)。This study was supported by National Natural Science Foundation of China(81473644),Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding Support(ZYLX201411),Project of Health Technical Personnel of Beijing Health System(2011-2-13).* Corresponding author,E-mail: zhss2000@ 163.com

        網(wǎng)絡出版時間: 2015-07-16 23∶15網(wǎng)絡出版地址: http:∥www.cnki.net/kcms/detail/11.3662.r.20150716.2315.029.html

        Effects of TongXie-YaoFang formula on serotonin and chromogranin a related transport mechanism of ion channels in colonic mucosa in diarrhea-predominant irritable bowel syndrome

        Zhang Shengsheng *,Yang Cheng

        (Center for Digestive Disease,Beijing Hospital of Traditional Chinese Medicine,Capital Medical University,Beijing 100010,China)

        【Abstract】Diarrhea-predominant irritable bowel syndrome(D-IBS)is a clinically common functional intestinal disease and it brings inconvenience to patients'live and work.TongXie-YaoFang(TXYF)formula,as a famous ancient prescription of Traditional Chinese Medicine,can significantly reduce the abdominal pain and diarrhea of D-IBS patients,thereby to improve the quality of their live and work.However,the exact mechanism is unclear.This article explores the influence of TXYF formula on ion channels of colon mucous membrane in D-IBS from the perspective of 5-HT and chromogranin A(CGA)related ion channel transport mechanism in order to provide reliable basis for subsequent clinical and basic research.

        【Key words】 TongXie-YaoFang(TXYF)formula; diarrhea-predominant irritable bowel syndrome(D-IBS); serotonin(5-HT); chromogranin A; ion channels; colonic mucosa

        Diarrhea-predominant irritable bowel syndrome(DIBS)is a chronic functional gastrointestinal disease and clinical manifestations are characterized by diarrhea,abdominal pain or discomfort with no organic gastrointestinal disorders.The diagnosis of D-IBS is based on symptom assessment and the Rome III criteria [1].It is believed that a combination of the Rome III criteria,blood tests,a physical examination,gastroscopy and colonoscopy with biopsies is considered necessary for diagnosis of D-IBS.In accordance with the epidemiologic data,DIBS mainly occurs in the young adults between 20 and 40 years of age and more often in women than in men [2].Currently,the pathogenesis of D-IBS has not been completely elucidated.With the“bio-psycho-social”medical model to be established,the pathogenesis of D-IBS seems to be multifactorial,with the following factors playing a central role in the pathogenesis of D-IBS: high visceral sensitivity,abnormal intestinal motility,brain-gut axis disorder,heritability and genetics,dietary/intestinal microbiota,low-grade inflammation,and disturbances in the neuroendocrine system(NES)of the gut [3-4].The usual treatment of Western medicine for the disease is symptomatic therapy which is not satisfactory to patients and increased use of health care resources simultaneously [5-6].However,alternative therapies,such as cognitive behavioural therapy and gut-directed hypnotherapy,have been used with good results [7].Traditional Chinese medicine(TCM)can significantly improve the patient's symptoms and the quality of life,more and more patients begin to seek treatment with TCM [8-9].

        1 Traditional Chinese medicine TongX-ie-Yaofang formula

        Tongxie Yaofang formula(TXYF)was created by Zhudanxi who was a famous Chinese medical scientist of the Yuan dynasty.TXYF is composed of Radix paeoniae alba,dried Tangerine Peel,Radix sileris and Atractylodes ovata.In recent years,there are more and more clinical studies and animal experiments about TXYF [10-12].However,the exact mechanism of the treatment of D-IBS is unclear.The authors will further explore the mechanism of TXYF’treatment for D-IBS on the basis of previous animal experiments [13].Recent studies have preliminarily showed that the mechanism of TXYF’treatment for D-IBS is via adjusting the colonic mucosa ion channels,changing the dynamics of the colon,and further affects the secretion and absorption of colonic mucosa.

        2 Serotonin(5 -hydroxytryptamine,5 -HT)

        5-HT is an important monoamine neurotransmitter in the hypothalamic-pituitary-adrenal(HPA)axis and plays significant physiopathological role in the secretion and absorption of colonic mucosa as well as in the contraction and relaxation of smooth muscle [14].According to the authoritative researches [15-17],5-HT3 receptors are widely distributed in the neurons of the gastrointestinal tract accounted for about 95%,as well as in the spinal cord and brain accounted for about 5%.The 5-HT3 receptor is a unique one which is a ligand-gated cation channel that belongs to the nicotine/γ-aminobutyric acid-receptor superfamily among the seven major subtypes,termed 5-HT1 to 5-HT7,while all the others are part of the family of G-protein-coupled receptors [17].The activation of gastrointestinal 5-HT3 receptors can lead to secretion and absorption of intestinal tract as well as peristaltic activity by stimulating the release of various neurotransmitters such as acetylcholine [18-19].Furthermore,it has been reported that selective 5-HT3-receptor antagonists,such as ramosetron,can effectively alleviate abdominal pain which is resulted from colonic distension,so that to illustrate that 5-HT3 receptors are involved in visceral nociceptive transmission [20].

        3 Chromogranin A(CGA)

        CGA,as a member of the nerve peptide family,is distributed within the chromaffin granules of neuroendocrine cells as well as in all neuroendocrine intracellular vesicles which can secrete catecholamine.At the same time,CGA is distributed in the intestinal endocrine tissues and participates in metabolism of the Ca 2+and catecholamine [3].It has been reported that the density of CGA-containing cells are lower in the duodenum of IBS patients [21]while the sensitivity and specificity at the cutoff<31 cells/mm 2in the duodenum are 91% and 89%,respectively [3].However,the density of CGA and CGA-containing cells in the colon tissues are unclear.An ongoing research shows that CGA is implicated as a potential mechanism of D-IBS and the density of CGA and CGA-containing cells in the colon tissues are lower in DIBS rats.CGA cell density may become a promising biomarker for the diagnosis of IBS.

        4 Hypothalamic-pituitary-adrenal(HPA)axis

        Recently,greater attention has been paid to the topic of dysregulation in HPA axis because of its importance in pathogenesis of D-IBS [22-23].According to a research conducted by Videlock et al. [23],HPA axis hyperresponsiveness to a visceral stressor which is correlative to a history of early adverse life events is more than to the existence of IBS.On the other hand,HPA axis reactivityhas a moderate effect on IBS symptoms.CGA and 5-hydroxytryptamine,as the regulatory factors of bowel function activity,play significant physiopathological roles in the secretion and absorption of colonic mucosa as well as in the motor and sensation of smooth muscle [14].Meanwhile,all of them play important roles in the HPA

        axis [2].

        5 Summary

        CGA and 5-hydroxytryptamine play significant physiopathological roles in the pathogenesis of D-IBS.The author have preliminarily reviewed the literature and explored that the interaction of CGA and 5-hydroxytryptamine maybe an important potential pathogenesis of D-IBS.However,it still need further research and further work to elucidate D-IBS mechanisms will focus on understanding how they interact.Although the details of TXYF’therapeutic mechanism of action remain to be clarified,TXYF has clear prospect for D-IBS therapy and may completely replace current treatments such as ramosetron.

        6 References

        [1] Drossman D A.Introduction.The Rome foundation and Rome III[J].Neurogastroenterol Motil,2007,19(10): 783-786.

        [2]Ian M C,Tamar R K,Temitope O K,et al.Molecular analys is of the luminal and mucosal associated intestinal microbiota in diarrhea-predominant irritable bowel syndrome [J].Am J Physiol Gastrointest Liver Physiol,2011,301(5): G799-G807.

        [3] Magdy E S.Irritable bowel syndrome: diagnosis and pathogenesis[J].World J Gastroenterol,2012,18(37): 5151-5163.

        [4] Per G F,Ami D S,Magnus S.Irritable bowel syndrome [J].Gastroenterol Res Pract,2012,2012: 612479.

        [5] Hungin A P,Whorwell P J,Tack J,et al.The prevalence,patterns and impact of irritable bowel syndrome: a international survey of 40,000 subjects[J].Aliment Pharmacol T-her,2003,17(5): 643-650.

        [6] Schnrich S,Brockow T,F(xiàn)ranke T,et al.Analyzing the content of outcome measures in clinical trails on irritable bowel syndrome using international classification of functioning disability and health as a reference[J].Rehabilitation(Stuttg),2006,45(3): 172-180.

        [7] Wald A,Rakel D.Behavioral and complementary approaches for the treatment of irritable bowel syndrome[J].Nutr Clin Pract,2008,23(3): 284-292.

        [8]張聲生,周濤,汪紅兵.腸易激綜合征中醫(yī)藥診療現(xiàn)狀與挑戰(zhàn)[J].世界華人消化雜志,2010,18(21): 2216-2220.

        [9] Zhang S S.Thinking and strategy on the diagnosis and treatment of functional gastrointestinal disorders with integrative medicine[J].Chin J Integr Med,2009,15(2): 83-85.

        [10]張聲生,許文君,汪正芳.抑肝扶脾法治療腹瀉型腸易激綜合征53例療效觀察[C].中華中醫(yī)藥學會脾胃病分會第二十三次全國脾胃病學術交流會論文匯編,2012: 373-377.

        [11]張濤,潘峰,徐建軍.痛瀉要方干預脾虛肝郁型大鼠腸易激綜合征的實驗研究[J].中成藥,2011,33(4): 687-689.

        [12]譚遠忠,熊麗萍.痛瀉要方加減聯(lián)合西藥治療腹瀉型腸易激綜合征臨床觀察[J].中國中西醫(yī)結合消化雜志,2012,20(9): 415-416.

        [13]張聲生,汪正芳,郭乾坤,等.疏肝健脾方對腹瀉型腸易激綜合征大鼠5-羥色胺相關的結腸黏膜上皮分泌功能的影響[J].中華中醫(yī)藥雜志,2012,32(11): 1516-1520.

        [14]Toshimi C,Kazunari Y,Shoko S,et al.Long-term efficacy and safety of ramosetron in the treatment of diarrhea-predominant irritable bowel syndrome[J].Clin Exp Gastroenterol,2013,25(6): 123-128.

        [15]Cremon C,Carini G,Wang B,et al.Intestinal serotonin release,sensory neuron activation,and abdominal pain in irritable bowel syndrome[J].Am J Gastroenterol,2011,106(7): 1290-1298.

        [16]Hirata T,Keto Y,Nakata M,et al.Effects of serotonin 5-HT3 receptor antagonists on stress-induced colonic hyperalgesia and diarrhoea in rats: a comparative study with opioid receptor agonists,a muscarinic receptor antagonist and a synthetic polymer[J].Neurogastroenterol Motil,2008,20(5): 557-565.

        [17]Frber L,Haus U,Spth M,et al.Physiology and pathophysiology of the 5-HT3 receptor[J].Scand J Rheumatol Suppl,2004,119: 2-8.

        [18]Wendy Atkinson,Lesley A.Houghton,Peter J.Whorwell,et al.Gender differences in plasma 5-hydroxytryptamine(5-HT)concentration in diarrhoea predominant irritable bowel syndrome(D-IBS): influence of the menstrual cycle[J].Gastroenterology,2003,124(4): 338.

        [19]Hirata T,F(xiàn)unatsu T,Keto Y,et al.Pharmacological profile of ramosetron,a novel therapeutic agent for IBS[J].In-flammopharmacology,2007,15(1): 5-9.

        [20]Mayer E A,Berman S,Derbyshire S W,et al.The effect of the 5-HT3 receptor antagonist,alosetron,on brain responses to visceral stimulation in irritable bowel syndrome patients[J].Aliment Pharmacol Ther,2002,16(7): 1357-1366.

        [21]El-Salhy M,Lomholt-Beck B,Hausken T.Chromogranin A as a possible tool in the diagnosis of irritable bowel syndrome[J].Scand J Gastroenterol,2010,45(12): 1435-1439.

        [22]Lineke M T,Anthony J C,Johan O,et al.Meta-analysis and meta-regression of hypothalamic-pituitary-adrenal axis activity in functional somatic disorders[J].Biol Psychol,2011,87(2): 183-194.

        [23]Videlock J E,Adeyemo M,Licudine A,et al.Childhood trauma is associated with hypothalamic-pituitary-adrenal axis responsiveness in irritable bowel syndrome[J].Gastroenterology,2009,137(6): 1954-1962.

        (收稿日期: 2012-02-11)

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