C-Phycocyanin prevents acute myocardial infarction-induced oxidative stress, inflammation and cardiac damage

被引:26
|
作者
Blas-Valdivia, Vanessa [1 ]
Nikita Moran-Dorantes, Daniela [2 ]
Rojas-Franco, Placido [2 ]
Franco-Colin, Margarita [2 ]
Mirhosseini, Neda [3 ]
Davarnejad, Reza [3 ]
Halajisani, Ahmad [4 ]
Tavakoli, Omid [5 ]
Cano-Europa, Edgar [2 ]
机构
[1] Inst Politecn Nacl, Dept Fisiol, Lab Neurobiol, Escuela Nacl Ciencias Biol, Ciudad De Mexico, Mexico
[2] Inst Politecn Nacl, Dept Fisiol, Lab Metabolismo 1, Escuela Nacl Ciencias Biol, Ciudad De Mexico, Mexico
[3] Arak Univ, Engn Fac, Chem Engn Dept, Arak, Iran
[4] Univ Tehran, Coll Engn, Caspian Fac Engn, Biofuel Lab, Tehran, Iran
[5] Univ Tehran, Coll Engn, Sch Chem Engn, Tehran, Iran
关键词
Phycobiliproteins; cardioprotection; anti-inflammatory; heart damage; cardiotoxicity; ENDOPLASMIC-RETICULUM STRESS; ARTHROSPIRA-MAXIMA SPIRULINA; KIDNEY; ANTIOXIDANT; INJURY; PATHOPHYSIOLOGY; BILIPROTEIN; APOPTOSIS; DISEASE;
D O I
10.1080/13880209.2022.2055089
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Context C-Phycocyanin is a protein with anti-scavenger, antioxidant and anti-inflammatory actions against agents that cause cellular damage. The cardioprotective action of C-phycocyanin against acute myocardial infarction (AMI) has not been studied in animal models. Objective To investigate C-phycocyanin's effect on oxidative stress, inflammation and cardiac damage in a model of isoproterenol-induced AMI. Materials and methods Wistar rats were divided into four groups: (1) sham + vehicle (0.9% saline solution by oral gavage, OG); (2) sham + C-phycocyanin (50 mg/kg/d, OG); (3) AMI + vehicle, and (4) AMI + C-phycocyanin. AMI was induced by administering isoproterenol (20, 10, 5 and 3 mg/kg each dose per day), and serum cardiac enzymes were quantified. After five days, the animals were euthanized; the heart was dissected to determine oxidative stress, redox environment, inflammation and cardiac damage markers. Results We observed that C-phycocyanin reduced AMI-increased cardiac enzymes (CK by about 53%, CKMB by about 60%, AST by about 16% and ALT by about 21%), lipid peroxidation (57%), reactive oxygen species (50%), nitrites (46%), oxidized glutathione (41%), IL1 beta (3%), INF gamma (5%), TNF alpha 3%), Bcl2 (37%), Bax (43%), COX2 (21%) and caspase 9 (61%). Finally, C-phycocyanin reduced AMI-induced aberrant histological changes related to myonecrosis, interstitial oedema and inflammatory infiltration in the heart muscle. Conclusions C-Phycocyanin prevents AMI-induced oxidative stress, inflammation and heart damage. This study is the first report that employed C-phycocyanin in an animal model of AMI and supports the potential use of C-phycocyanin in the management of AMI.
引用
收藏
页码:755 / 763
页数:9
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