Zhaojie Li1 ,
Mingzhi Long2,
Kai Li1,
Yanfeng Liu1,
Xin Shang3
1Department of Emergency, The First Affiliate Hospital of Xi'an Medical University, Xi’an, Shaanxi 710077;
2Department of Cardiovascular Medicine, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210011;
3Department of Internal Medicine, Xi'an Traditional Chinese Medicine Hospital, Xi'an, Shaanxi 710021, China.
For correspondence:- Zhaojie Li
Email: LCannypazos@yahoo.com Tel:+862984277592
Accepted: 18 July 2018
Published: 31 August 2018
Citation:
Li Z, Long M, Li K, Liu Y, Shang X.
In vitro and in vivo antiseptic activities of caffeoylquinic acid. Trop J Pharm Res 2018; 17(8):1657-1661
doi:
10.4314/tjpr.v17i8.27
© 2018 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Abstract
Purpose: To evaluate the antiseptic effect of caffeoylquinic acid (CA) in in vivo and in vitro models.
Methods: In vivo sepsis was produced in rats via cecal ligation and puncture (CLP) method. Four groups of rats were used: control group, untreated CLP group, and two CA groups treated with caffeoylquinic acid (50 and 100 mg/kg, p.o.) for 30 days before the induction of sepsis. Following the induction of sepsis, histological assessment of lung tissue was carried out using hematoxylin and eosin, and isolectin B4 staining. In addition, in vitro tests were performed on RAW264.7 cells in which inflammation and oxidative stress were induced by lipopolysaccharide (LPS).
Results: Treatment with CA significantly (p < 0.05) enhanced the survival of lung cells, relative to the CLP group. Lung histopathology revealed that pretreatment with CA did not attenuate the increased infiltration of macrophages in the alveoli. Results from in vitro studies showed that CA attenuated LPS-induced nitric oxide (NO) levels, but had no significant effect on the level of LPS-induced pro-inflammatory cytokines in RAW264.7 cells (p < 0.05).
Conclusion: These results reveal that CA attenuates NO and TNF-α levels in LPS-stimulated macrophages, thereby decreasing inflammation-associated sepsis. Thus, CA may have beneficial effects on lung injury as a result of its antioxidant and anti-inflammatory activities.
Keywords: Caffeoylquinic acid, Sepsis, Oxidative stress, Cytokines, Cecalligation, Puncture