Molecular mechanisms behind the biological effects of hesperidin and hesperetin for the prevention of cancer and cardiovascular diseases

被引:309
作者
Roohbakhsh, Ali [1 ]
Parhiz, Hamideh [1 ,2 ]
Soltani, Fatemeh [2 ,3 ,4 ]
Rezaee, Ramin [1 ,4 ]
Iranshahi, Mehrdad [3 ]
机构
[1] Mashhad Univ Med Sci, Sch Pharm, Pharma Res Ctr, Mashhad, Iran
[2] Mashhad Univ Med Sci, Sch Pharm, Dept Pharmaceut Biotechnol, Mashhad, Iran
[3] Mashhad Univ Med Sci, Sch Pharm, Biotechnol Res Ctr, Mashhad, Iran
[4] North Khorasan Univ Med Sci, Sch Med, Dept Mol Sci, Bojnurd, Iran
关键词
Flavonoid; Anti-cancer; Anticoagulant; Hesperetin; GLUCOSYL HESPERIDIN; LUNG CARCINOGENESIS; CITRUS FLAVONOIDS; BETA-CRYPTOXANTHIN; ANTIOXIDANT STATUS; OXIDATIVE STRESS; GENE-EXPRESSION; UP-REGULATION; NITRIC-OXIDE; KAPPA-B;
D O I
10.1016/j.lfs.2014.12.030
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Hesperidin (Hsd) and its aglycone, hesperetin (Hst), are two flavonoids from citrus species that have various biological properties, particularly those for the prevention of cancer and cardiovascular diseases. Studies have shown both anti-cancer and cancer chemopreventive effects for Hsd and Hst Cancer chemopreventive properties of Hsd and Hst are mainly associated with their antioxidant, radical scavenging and anti-inflammatory activities. In addition, Hsd and Hst interfere at different stages of cancer. Unlike conventional anti-cancer drugs, Hsd and Hst inhibit tumor growth by targeting multiple cellular protein targets at the same time, including caspases, Bcl-2 (B-cell lymphoma 2) and Bax (Bcl-2 associated X protein) for the induction of apoptosis, and COX-2 (cyclooxygenase-2), MMP-2 (matrix metalloproteinase-2) and MMP-9 for the inhibition of angiogenesis and metastasis. The results of the recent basic and clinical studies revealed the beneficial effects for Hst, Hsd and their derivatives in the treatment of heart failure and cardiac remodeling, myocardial ischemia and infarction, and hypertension. In addition, the valuable effects of Hst and Hsd in the treatment of diabetes and dyslipidemia with their anti-platelet and anticoagulant effects make them good candidates in the treatment of various cardiovascular diseases. In this review, new findings regarding the molecular targets of Hsd and Hst, animal studies and clinical trials are discussed. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:64 / 74
页数:11
相关论文
共 91 条
[1]
Hesperidin blunts streptozotocin-isoproternol induced myocardial toxicity in rats by altering of PPAR-γ receptor [J].
Agrawal, Yogeeta O. ;
Sharma, Pankaj Kumar ;
Shrivastava, Birendra ;
Arya, Dharamvir Singh ;
Goyal, Sameer N. .
CHEMICO-BIOLOGICAL INTERACTIONS, 2014, 219 :211-220
[2]
Ahmed OM, 2011, LIFE SCI J, V8, P91
[3]
Hypoglycemic and Hypolipidemic Effects of Hesperidin and Cyclodextrin-Clathrated Hesperetin in Goto-Kakizaki Rats with Type 2 Diabetes [J].
Akiyama, Satoko ;
Katsumata, Shin-ichi ;
Suzuki, Kazuharu ;
Nakaya, Yumi ;
Ishimi, Yoshiko ;
Uehara, Mariko .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2009, 73 (12) :2779-2782
[4]
Antioxidant capacity of hesperidin from Citrus peel using electron spin resonance and cytotoxic activity against human carcinoma cell lines [J].
Al-Ashaal, Hanan A. ;
El-Sheltawy, Shakinaz T. .
PHARMACEUTICAL BIOLOGY, 2011, 49 (03) :276-282
[5]
[Anonymous], 2011, Biomed Prevent Nutr, DOI DOI 10.1016/J.BIONUT.2011.06.004
[6]
[Anonymous], PHYTOTHER RES S1
[7]
[Anonymous], 2011, Biomed. Aging Pathol., DOI DOI 10.1016/J.BIOMAG.2011.09
[8]
Efficacy of the potential chemopreventive agent, hesperetin (citrus flavanone), on 1,2-dimethylhydrazine induced colon carcinogenesis [J].
Aranganathan, S. ;
Nalini, N. .
FOOD AND CHEMICAL TOXICOLOGY, 2009, 47 (10) :2594-2600
[9]
Hesperetin exerts dose dependent chemopreventive effect against 1,2-dimethyl hydrazine induced rat colon carcinogenesis [J].
Aranganathan, Selvaraj ;
Selvam, Jayabal Panneer ;
Nalini, Namasivayam .
INVESTIGATIONAL NEW DRUGS, 2009, 27 (03) :203-213
[10]
Cyclic nucleotide phosphodiesterases: Molecular regulation to clinical use [J].
Bender, Andrew T. ;
Beavo, Joseph A. .
PHARMACOLOGICAL REVIEWS, 2006, 58 (03) :488-520