The Alleviating Effects and the Underlying Mechanism of the Total Glucosides from Paeonia lactiflora on Irritable Bowel Syndrome
XU Ping-xiang1, GE Bei-kang1, YANG Jia-wen1, YAN Wei-jie1, MA Yi1, TIAN Hui2, XUE Ming1*
1. Department of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing 100069, China; 2. Wonner Biotechnology Company, Beijing 100069, China
Abstract��OBJECTIVE To clarify the effect of total glucosides from paeony(PTG) on irritable bowel syndrome (IBS), and to explore the molecular mechanism of PTG on alleviating diarrhea symptoms and abdominal pain.METHODS The diarrhea model was conducted by exposing rat to restraint stress stimulation and bellyache model was conducted by subcutaneous injection of neostigmine to mice. Based on these two models, the curative effect of PTG on IBS was investigated. To investigate the regulative effects of PTG on Caco-2 cells, the Caco-2 monolayer cell model with barrier dysfunction was established by trypsin stimulation, and the inflammatory Caco-2 cell model was established by interleukin-1�� (IL-1��) stimulation.RESULTS PTG could significantly reduce the frequency of defecation in diarrhea rat model (P<0.05) and relieve abnormal bowel movements in bellyache mice model (P<0.05). After PTG treatment, the TEER value of Caco-2 monolayer was significantly increased (P<0.01), the transmittance of fluorescence yellow was significantly decreased (P<0.001) and the expression of tight junction (ZO-1)protein was notably up-regulated (P<0.001). In addition, the gene and protein expression of nuclear factor profilin kappa B(I��B��)in inflammatory Caco-2 cell model was significantly improved (P<0.001) after PTG treatment.CONCLUSION PTG significantly ameliorates IBS symptoms by protecting the barrier function of Caco-2 cell monolayer and relieving inflammation of Caco-2 cells.
��ƽ��, �𱴿�, ������, ��ΰ��, ����, ����, Ѧ��. ��ҩ���ջ������ʵ���Գ����ۺ��������ü������о�[J]. �й�ҩѧ��־, 2018, 53(23): 2014-2020.
XU Ping-xiang, GE Bei-kang, YANG Jia-wen, YAN Wei-jie, MA Yi, TIAN Hui, XUE Ming. The Alleviating Effects and the Underlying Mechanism of the Total Glucosides from Paeonia lactiflora on Irritable Bowel Syndrome. Chinese Pharmaceutical Journal, 2018, 53(23): 2014-2020.
LANG S, FEI L, XU W, et al. Effect of chronic stress on irritable bowel syndrome. J Chongqing Med Uni(����ҽ�ƴ�ѧѧ��), 2018, 43(1):1-5.
[2]
LIANG R, GE W, WANG H, et al. Effect of ��TONG XIE YAO FANG�� on irritable bowel syndrome and gut-brain axis. Chin J Exp Tradit Med(�й�ʵ�鷽��ѧ��־), 2018,24(2):152-157.
[3]
WU H, AO H,HUANG S, et al. Mechanism of Shuganjianpi decoction on visceral hypersensitivity of rats with irritable bowel syndrome. Chin J Trad Chin Med (�л���ҽҩ��־), 2018,33(1):317-320.
[4]
CUI H, ZHU J, FENG Q, et al. The chemical properties and bioactivity of traditional Chinese Herb Paeonia. Strait Pharm J(��Ͽҩѧ), 2017, 29(9):1-5.
[5]
LIN F, WANG J, HU Y, et al. Effect of total glucosides of paeonia on TGF-��1 and ICAM-1 expression in the kidney of diabetic rats. Intern J Clin Exp Path, 2016, 9(2):620-626.
[6]
ZHANG X, LI Z, LEUNG W, et al. The analgesic effect of paeoniflorin on neonatal maternal separation-induced visceral hyperalgesia in rats. J Pain, 2008, 9(6):497-505.
[7]
WILLAMS C L, VILLAR R G, PETERSON J M, et al. Stress-induced changes in intestinal transit in the rat: a model for irritable bowel syndrome. Gastroenterology, 1988, 94(3):611-621.
[8]
ZENG H, ZHOU Q G, LUO T, et al. Comparison of the effects of honokiol and honokiol on diarvhea and gastrointestinal emptying in mice. Chin Herbal Med(��ҩ��), 2015, 38(10):2160-2162.
[9]
WANG F, YANG X. The absorption and transportation of isoflavonol in Caco-2 monolayer model . China J Chin Mater Med(�й���ҩ��־), 2017, 42(16):3206-3212.
[10]
WANG H, TONG J, WANG B. Effect of ethanol on the expression of ZO-1 in epithelial cell. Shanxi Med J (ɽ��ҽҩ��־), 2012,41(9):858-860.
[11]
CHAI Y, GUO Z, DU Q, et al. Effect of Kuijiling on the expression of E1, UBC5 and E3RSIBZO-1 in Caco-2 inflammatory cell model. Pharmacol Clin Chin Mater Med(��ҩҩ�����ٴ�), 2012, 28(5):137-140.
[12]
CHAI Y, DU Q, LI Y, et al. Effect of Kuijiling on the expression of NF-��B in Caco-2 inflammatory cell model. Pharmacol Clin Chin Mater Med(��ҩҩ�����ٴ�),2013, 24(1):14-17.
[13]
XU W, ZHAO Y, QIN Y, et al. Comparison of paeonia pharmacokinetics in rats under normoxia and hypoxia. Inter J Pharm Res(����ҩѧ�о���־), 2016, 43(2):336-340.
[14]
ZHOU Z, YI J, WANG Z. Effect of Shaoyao-Gancao Decoction on visceral hypersensitivity of rats with irritable bowel syndrome. Chin J Integr Tradit Chin West Med (�й�����ҽ�����־), 2017, 37(5):575-578.
[15]
GECSE K, ROKA R, FERRIER L, et al. Increased faecal serine protease activity in diarrhoeic IBS patients: a colonic lumend factor impairing colonic permeability and sensitivity. Gut, 2008,57(5):591-599.
[16]
COMPTON P, GRIFFIS C, BREEN E, et al. Opioid treatment of experimental pain activates nuclear factor-��B. J Opioid Manag, 2015, 11(2):115.