Effects of CDP-Choline and Choline on COX Pathway in LPS-Induced Inflammatory Response in Rats

被引:8
作者
Baris, E. [1 ,2 ]
Simsek, O. [1 ]
Efe, H. [3 ]
Oncu, S. [4 ]
Gelal, A. [4 ]
Hamurtekin, E. [5 ]
Tosun, M. [2 ]
Ozbal, S. [6 ]
Yuce, Z. [3 ]
Arici, M. A. [4 ]
机构
[1] Dokuz Eylul Univ, Grad Sch Hlth Sci, Izmir, Turkey
[2] Izmir Univ Econ, Dept Pharmacol, Fac Med, Izmir, Turkey
[3] Dokuz Eylul Univ, Dept Med Biol, Fac Med, Izmir, Turkey
[4] Dokuz Eylul Univ, Dept Pharmacol, Fac Med, Izmir, Turkey
[5] Eastern Mediterranean Univ, Dept Pharmacol, Fac Med, Izmir, Turkey
[6] Dokuz Eylul Univ, Med Sci, Fac Med, Dept Histol & Embryol, Izmir, Turkey
关键词
CDP-choline; choline; lipopolysaccharide; cyclooxygenase; 2; cholinergic anti-inflammatory pathway; endotoxemia; prostaglandin levels; ANTIINFLAMMATORY PATHWAY; ORGAN INJURY; RECEPTOR; HYPOTENSION; INVOLVEMENT; ENDOTOXIN; SURVIVAL; IMPROVES; SEPSIS; MODEL;
D O I
10.3923/ijp.2021.84.96
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and Objective: Cytidine-5-diphosphate-choline (CDP-choline) and choline activate the cholinergic anti-inflammatory pathway in case of inflammation. This study investigated the role of CDP-choline and choline along with the contribution of the cyclooxygenase (COX) pathway on the lipopolysaccharide (LPS)-induced endotoxemia model in rats. Materials and Methods: Endotoxemia model was induced by LPS administration. CDP-choline or choline 5 min before and 6 hrs after LPS injection. The sepsis severity, body weight changes, survival rate were evaluated. Serum prostaglandins, Tumour Necrosis Factor (TNF)-alpha, total choline levels were measured. COX-2 mRNA expression and protein levels were analyzed. Spleen tissues were evaluated histomorphological. One-way analysis of variance analysis (ANOVA) or Kruskal Wallis tests was used for statistical analysis. Results: COX-2 expressions in liver and brain tissues, serum prostaglandin E-2, 6-keto prostaglandin F-1 alpha, Thromboxane A(2) and TNF alpha levels were increased 24 hrs after LPS administration. Administrations of CDP-choline or choline were decreased COX-2 expression in the liver. Serum prostaglandin levels were decreased in the CDP-choline-treated group, whereas, only prostaglandin E-2 level was decreased in the choline-treated group. Total choline levels in serum and brain were increased after CDP-choline or choline administration. Accordingly, serum TNF alpha levels and TNF alpha expression in the liver were decreased in CDP-choline and choline-treated groups. TNF alpha expression in the brain was decreased in the choline-treated group, whereas, increased in the CDP-choline-treated group. Conclusion: CDP-choline and choline decreased LPS-induced COX-2 enzyme expression and prostaglandin levels in the periphery by increasing serum and brain total choline levels in the LPS-induced endotoxemia model in rat.
引用
收藏
页码:84 / 96
页数:13
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