PMID- 25298580 OWN - NLM STAT- MEDLINE DCOM- 20150611 LR - 20211021 IS - 1998-3751 (Electronic) IS - 0253-7613 (Print) IS - 0253-7613 (Linking) VI - 46 IP - 5 DP - 2014 Sep-Oct TI - Effects of tongxinluo on the neointima formation and expression of inflammatory cytokines in rats after carotid artery balloon injury. PG - 510-4 LID - 10.4103/0253-7613.140582 [doi] AB - OBJECTIVE: Tongxinluo (TXL) is a traditional Chinese medicine (TCM). It is used to treat coronary heart disease and atherosclerosis. We investigated the effects of TXL on the neointima formation and expression of inflammatory cytokines in rats after carotid artery balloon injury. MATERIALS AND METHODS: Male Sprague-Dawley rats were randomly divided into four groups: sham operation group (Sham, n = 15), balloon injury group treated with vehicle (Control, n = 15), TXL low-dose group treated with TXL of 0.5 g/kg/d (TXL-L, n = 15), and TXL high-dose group treated with TXL of 1.0 g/kg/d (TXL-H, n = 15). TXL was given by gavage daily. 14 days after injury', the levels of serum nitric oxide (NO), endothelin-1 (ET-1), monocyte chemoattractant protein-1 (MCP-1), and soluble intercellular adhesion molecule-1 (sICAM-1) were evaluated. The morphology of carotid artery tissue was observed with hematoxylin-eosin staining. Expressions of MCP-1 and ICAM-1 in the artery were detected by real-time polymerase chain reaction (RT-PCR) and western blotting. RESULTS: 14 days after injury, a significant increase in concentrations of serum ET-1, MCP-1, and sICAM-1 (P < 0.05), as well as a significant decrease in NO serum level were observed in rats subjected to artery injury compared to the sham rats (P < 0.05). TXL significantly decreased ET-1, MCP-1 and sICAM-1 serum levels (P < 0.05), whereas significantly increased NO serum level compared with the control (P < 0.05). TXL significantly reduced the neointimal thickening at day14 after injury (P < 0.05). In addition, TXL significantly reduced mRNA and protein expressions of ICAM-1 and MCP-1 in injured artery (P < 0.05). CONCLUSIONS: This study demonstrates that TXL is effective in improving endothelial function, attenuating neointimal formation of artery after balloon injury, and reducing expression of inflammatory cytokine MCP-1 and ICAM-1. It may be a useful agent for protecting the artery against injury. FAU - Yao, En-Hui AU - Yao EH AD - Department of Cardiology, Union Hospital of Fujian Medical University, Fujian Institute of Coronary Artery Disease, Fuzhou, China. FAU - Wang, Hua-Jun AU - Wang HJ AD - Fujian Hypertension Research Institute, the First Affiliated Hospital of Fujian Medical University, Fuzhou, China. FAU - Xu, Chang-Sheng AU - Xu CS AD - Fujian Hypertension Research Institute, the First Affiliated Hospital of Fujian Medical University, Fuzhou, China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - India TA - Indian J Pharmacol JT - Indian journal of pharmacology JID - 7902477 RN - 0 (Ccl2 protein, rat) RN - 0 (Chemokine CCL2) RN - 0 (Cytokines) RN - 0 (Drugs, Chinese Herbal) RN - 0 (Inflammation Mediators) RN - 0 (RNA, Messenger) RN - 0 (tongxinluo) RN - 126547-89-5 (Intercellular Adhesion Molecule-1) SB - IM MH - Animals MH - Blotting, Western MH - Carotid Artery Injuries/*drug therapy/pathology MH - Chemokine CCL2/blood/drug effects/genetics MH - Cytokines/drug effects/genetics/metabolism MH - Disease Models, Animal MH - Dose-Response Relationship, Drug MH - Drugs, Chinese Herbal/administration & dosage/*pharmacology MH - Endothelium, Vascular/drug effects/pathology MH - Gene Expression Regulation/drug effects MH - Inflammation Mediators/metabolism MH - Intercellular Adhesion Molecule-1/blood/drug effects/genetics MH - Male MH - Neointima/*prevention & control MH - RNA, Messenger MH - Rats MH - Rats, Sprague-Dawley MH - Real-Time Polymerase Chain Reaction PMC - PMC4175887 OTO - NOTNLM OT - Carotid artery injury OT - inflammatory cytokine OT - neointima formation OT - tongxinluo COIS- Conflict of Interest: No EDAT- 2014/10/10 06:00 MHDA- 2015/06/13 06:00 PMCR- 2014/09/01 CRDT- 2014/10/10 06:00 PHST- 2013/12/15 00:00 [received] PHST- 2014/03/15 00:00 [revised] PHST- 2014/07/26 00:00 [accepted] PHST- 2014/10/10 06:00 [entrez] PHST- 2014/10/10 06:00 [pubmed] PHST- 2015/06/13 06:00 [medline] PHST- 2014/09/01 00:00 [pmc-release] AID - IJPharm-46-510 [pii] AID - 10.4103/0253-7613.140582 [doi] PST - ppublish SO - Indian J Pharmacol. 2014 Sep-Oct;46(5):510-4. doi: 10.4103/0253-7613.140582.