Please use this identifier to cite or link to this item: https://doi.org/10.1155/2017/5864945
Title: Chai-Qin-Cheng-Qi Decoction and Carbachol Improve Intestinal Motility by Regulating Protein Kinase C-Mediated Ca2+ Release in Colonic Smooth Muscle Cells in Rats with Acute Necrotising Pancreatitis
Authors: Zhang, C.-L
Lin, Z.-Q
Luo, R.-J
Zhang, X.-X
Guo, J
Wu, W
Shi, N
Deng, L.-H
Chen, W.-W
Zhang, X.-Y
Bharucha, S
Huang, W
Sutton, R
Windsor, J.A 
Xue, P
Xia, Q
Keywords: adenylate cyclase
arginine
calcium ion
carbachol
chai qin cheng qi decoction
fatty acid binding protein 2
messenger RNA
motilin
phospholipase C beta1
plant medicinal product
protein kinase C
protein kinase C alpha
substance P
unclassified drug
vasoactive intestinal polypeptide
acute hemorrhagic pancreatitis
adult
agar gel electrophoresis
animal experiment
animal model
animal tissue
Article
calcium cell level
calcium transport
cell death
cell infiltration
cell isolation
colonic muscle
comparative study
controlled study
disease severity
down regulation
fluorescence
histopathology
inflammatory cell
intestinal dysmotility
intestine motility
male
nonhuman
protein expression
rat
smooth muscle cell
upregulation
Western blotting
Issue Date: 2017
Citation: Zhang, C.-L, Lin, Z.-Q, Luo, R.-J, Zhang, X.-X, Guo, J, Wu, W, Shi, N, Deng, L.-H, Chen, W.-W, Zhang, X.-Y, Bharucha, S, Huang, W, Sutton, R, Windsor, J.A, Xue, P, Xia, Q (2017). Chai-Qin-Cheng-Qi Decoction and Carbachol Improve Intestinal Motility by Regulating Protein Kinase C-Mediated Ca2+ Release in Colonic Smooth Muscle Cells in Rats with Acute Necrotising Pancreatitis. Evidence-based Complementary and Alternative Medicine 2017 : 5864945. ScholarBank@NUS Repository. https://doi.org/10.1155/2017/5864945
Rights: Attribution 4.0 International
Abstract: Chai-Qin-Cheng-Qi decoction (CQCQD) improves intestinal motility in acute pancreatitis (AP), but the mechanism(s) require elucidation. We investigated the effects of CQCQD and carbachol, a prokinetic agent, on colonic smooth muscle cells (SMCs) in L-arginine-induced necrotising AP model in rats. In treatment groups, intragastric CQCQD (20 g/kg, 2 hourly × 3 doses) or intraperitoneal carbachol (60 μg/kg) was given 24 hours after induction of AP. Both CQCQD and carbachol decreased the severity of pancreatic and colonic histopathology (all P<0.05). Both CQCQD and carbachol reduced serum intestinal fatty acid binding protein, vasoactive intestinal peptide, and substance P and increased motility levels. CQCQD upregulated SMC phospholipase C-beta 1 (PLC-β1) mRNA and PLC protein (both P<0.05), while both treatments upregulated protein kinase C-alpha (PKC-α) mRNA and PKC protein and downregulated adenylate cyclase (AC) mRNA and protein compared with no treatment (all P<0.05). Neither treatment significantly altered L-arginine-induced PKC-β1 and PKC-ϵ mRNA reduction. Both treatments significantly increased fluorescence intensity of SMC intracellular calcium concentration [Ca2+]i (3563.5 and 3046.9 versus 1086.9, both P<0.01). These data suggest CQCQD and carbachol improve intestinal motility in AP by increasing [Ca2+]i in colonic SMCs via upregulating PLC, PKC and downregulating AC. © 2017 Chen-Long Zhang et al.
Source Title: Evidence-based Complementary and Alternative Medicine
URI: https://scholarbank.nus.edu.sg/handle/10635/179884
ISSN: 1741427X
DOI: 10.1155/2017/5864945
Rights: Attribution 4.0 International
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