Please use this identifier to cite or link to this item: https://doi.org/10.1155/2017/5864945
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dc.titleChai-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
dc.contributor.authorZhang, C.-L
dc.contributor.authorLin, Z.-Q
dc.contributor.authorLuo, R.-J
dc.contributor.authorZhang, X.-X
dc.contributor.authorGuo, J
dc.contributor.authorWu, W
dc.contributor.authorShi, N
dc.contributor.authorDeng, L.-H
dc.contributor.authorChen, W.-W
dc.contributor.authorZhang, X.-Y
dc.contributor.authorBharucha, S
dc.contributor.authorHuang, W
dc.contributor.authorSutton, R
dc.contributor.authorWindsor, J.A
dc.contributor.authorXue, P
dc.contributor.authorXia, Q
dc.date.accessioned2020-10-26T04:57:56Z
dc.date.available2020-10-26T04:57:56Z
dc.date.issued2017
dc.identifier.citationZhang, 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
dc.identifier.issn1741427X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179884
dc.description.abstractChai-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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectadenylate cyclase
dc.subjectarginine
dc.subjectcalcium ion
dc.subjectcarbachol
dc.subjectchai qin cheng qi decoction
dc.subjectfatty acid binding protein 2
dc.subjectmessenger RNA
dc.subjectmotilin
dc.subjectphospholipase C beta1
dc.subjectplant medicinal product
dc.subjectprotein kinase C
dc.subjectprotein kinase C alpha
dc.subjectsubstance P
dc.subjectunclassified drug
dc.subjectvasoactive intestinal polypeptide
dc.subjectacute hemorrhagic pancreatitis
dc.subjectadult
dc.subjectagar gel electrophoresis
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectcalcium cell level
dc.subjectcalcium transport
dc.subjectcell death
dc.subjectcell infiltration
dc.subjectcell isolation
dc.subjectcolonic muscle
dc.subjectcomparative study
dc.subjectcontrolled study
dc.subjectdisease severity
dc.subjectdown regulation
dc.subjectfluorescence
dc.subjecthistopathology
dc.subjectinflammatory cell
dc.subjectintestinal dysmotility
dc.subjectintestine motility
dc.subjectmale
dc.subjectnonhuman
dc.subjectprotein expression
dc.subjectrat
dc.subjectsmooth muscle cell
dc.subjectupregulation
dc.subjectWestern blotting
dc.typeArticle
dc.contributor.departmentSURGERY
dc.description.doi10.1155/2017/5864945
dc.description.sourcetitleEvidence-based Complementary and Alternative Medicine
dc.description.volume2017
dc.description.page5864945
dc.published.statePublished
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