The Interaction between Arachidonic Acid Metabolism and Homocysteine

被引:10
作者
Domi, Elisa [1 ]
Hoxha, Malvina [1 ]
Hoxha, Bianka [1 ]
Zappacosta, Bruno [1 ]
机构
[1] Catholic Univ Our Lady Good Counsel, Fac Pharm, Dept Chem Toxicol & Pharmacol Evaluat Drugs, Rruga Dritan Hoxha, Tirana, Albania
关键词
Homocysteine; hyperhomocysteinemia; arachidonic acid; cardiovascular diseases; epoxyeicosatrienoic acids; Homeostasis; SOLUBLE EPOXIDE HYDROLASE; INFLAMMATORY MARKERS; RISK-FACTOR; HYPERHOMOCYSTEINEMIA; DISEASE; PROSTACYCLIN; EXPRESSION; PATHWAY; BRAIN; CYCLOOXYGENASE-2;
D O I
10.2174/1871530320999200904130504
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hyperhomocysteinemia (HHcy) has been considered a risk factor for different diseases, including cardiovascular disease (CVD), inflammation, neurological diseases, cancer, and many other pathological conditions. Likewise, arachidonic acid (AA) metabolism is implicated in both vascular homeostasis and inflammation, as shown by the development of CVD, following the imbalance of its metabolites. This review summarizes how homocysteine (Hcy) can influence the metabolism of AA. In silico literature searches were performed on PubMed and Scopus as main sources. Several studies have shown that altered levels of Hcy, through AA release and metabolism, can influence the synthesis and the activity of prostaglandins (PGs), prostacyclin (PGI2), thromboxane (TXA), epoxyeicosatrienoic acids (EETs), and hydroxyeicosatetraenoic acids (HETEs). It is believed that by targeting Hcy in the AA pathways, novel compounds with better pharmacological and pharmacodynamics benefits may be obtained and that this information is valuable for a dietician to manipulate diets to improve health.
引用
收藏
页码:1232 / 1241
页数:10
相关论文
共 105 条
[1]   Dynamics of arachidonic acid mobilization by inflammatory cells [J].
Astudillo, Alma M. ;
Balgoma, David ;
Balboa, Maria A. ;
Balsinde, Jesus .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2012, 1821 (02) :249-256
[2]   Hyperhomocysteinemia in patients with cardiovascular disease [J].
Baszczuk, Aleksandra ;
Kopczynski, Zygmunt .
POSTEPY HIGIENY I MEDYCYNY DOSWIADCZALNEJ, 2014, 68 :579-589
[3]   Hypoxia signaling to genes - Significance in Alzheimer's disease [J].
Bazan, NG ;
Palacios-Pelaez, R ;
Lukiw, WJ .
MOLECULAR NEUROBIOLOGY, 2002, 26 (2-3) :283-298
[4]  
Bellinghieri G, 2008, J NEPHROL, V21, pS113
[5]   n-3 polyunsaturated fatty acids, inflammation, and inflammatory diseases [J].
Calder, Philip C. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2006, 83 (06) :1505S-1519S
[6]  
Capdevila JH, 2000, J LIPID RES, V41, P163
[7]   Folic Acid and Vitamin B12 Administration in CKD, Why Not? [J].
Capelli, Irene ;
Cianciolo, Giuseppe ;
Gasperoni, Lorenzo ;
Zappulo, Fulvia ;
Tondolo, Francesco ;
Cappuccilli, Maria ;
La Manna, Gaetano .
NUTRIENTS, 2019, 11 (02)
[8]   Cysteinyl-leukotrienes and their receptors in asthma and other inflammatory diseases: Critical update and emerging trends [J].
Capra, Valerie ;
Thompson, Miles D. ;
Sala, Angelo ;
Cole, David E. ;
Folco, Giancarlo ;
Rovati, G. Enrico .
MEDICINAL RESEARCH REVIEWS, 2007, 27 (04) :469-527
[9]   Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: An overview [J].
Castro, R ;
Rivera, I ;
Blom, HJ ;
Jakobs, C ;
de Almeida, IT .
JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 (01) :3-20
[10]   P2Y12 receptor blockade synergizes strongly with nitric oxide and prostacyclin to inhibit platelet activation [J].
Chan, Melissa V. ;
Knowles, Rebecca B. M. ;
Lundberg, Martina H. ;
Tucker, Arthur T. ;
Mohamed, Nura A. ;
Kirkby, Nicholas S. ;
Armstrong, Paul C. J. ;
Mitchell, Jane A. ;
Warner, Timothy D. .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2016, 81 (04) :621-633