Premium
Carnosine protects brain microvascular endothelial cells against rotenone‐induced oxidative stress injury through histamine H 1 and H 2 receptors in vitro
Author(s) -
Zhang Luyi,
Yao Ke,
Fan Yanying,
He Ping,
Wang Xiaofen,
Hu Weiwei,
Chen Zhong
Publication year - 2012
Publication title -
clinical and experimental pharmacology and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 103
eISSN - 1440-1681
pISSN - 0305-1870
DOI - 10.1111/1440-1681.12019
Subject(s) - carnosine , rotenone , pyrilamine , oxidative stress , histamine , histamine receptor , chemistry , pharmacology , apoptosis , receptor , biochemistry , biology , mitochondrion , antagonist
SummaryAlthough it is believed that carnosine has protective effects on various cell types, its effect on microvascular endothelial cells has not been well defined. In the present study, we investigated the protective effects of carnosine in microvascular endothelial cells using an in vitro rotenone‐induced oxidative stress model. Mouse brain microvascular endothelial cells were exposed to 1 μmol/L rotenone for 18 h. In some experiments, carnosine (100 nmol/L–1 mmol/L) was added 30 min prior to rotenone exposure. When used, histamine receptor antagonists (100 nmol/L–10 μmol/L) were added 15 min before carnosine treatment. After rotenone exposure, apoptosis of microvascular cells was analysed by H oechst 33342 staining, whereas mitochondrial membrane potential was assessed by JC ‐1 staining. Intracellular carnosine and histamine levels were determined using HPLC or ultra‐ HPLC . Over the range 1 μmol/L–1 mmol/L, carnosine concentration‐dependently decreased the number of apoptotic cells after 18 h exposure to rotenone. This effect was reversed by the histamine H 1 receptor antagonists pyrilamine and diphenhydramine (1 and 10 μmol/L) and the H 2 receptor antagonists cimetidine (100 nmol/L–10 μmol/L) and zolatidine (10 μmol/L). α‐Fluoromethylhistidine (100 μmol/L), a selective and irreversible inhibitor of histidine decarboxylase, also significantly inhibited the protective effects of carnosine. At 0.1 mmol/L, carnosine restored the decrease in mitochondrial membrane potential after 6 h exposure to 1 μmol/L rotenone and this effect was also reversed by the H 1 and H 2 receptor antagonists. Moreover, intracellular carnosine levels increased as early as 1 h after carnosine treatment, whereas intracellular histamine levels increased 18 h after carnosine treatment. The results of the present study indicate that carnosine protects brain microvascular endothelial cells against rotenone‐induced oxidative stress injury via histamine H 1 and H 2 receptors. The findings suggest that carnosine may be beneficial in the treatment of microvascular endothelial dysfunction induced by oxidative stress.