Pomegranate flower:: a unique traditional antidiabetic medicine with dual PPAR-α/-γ activator properties

被引:153
作者
Li, Yuhao [1 ]
Qi, Yanfei [1 ]
Huang, Tom H. W. [1 ]
Yamahara, Johji [2 ]
Roufogalis, Basil D. [1 ]
机构
[1] Univ Sydney, Fac Pharm, Sydney, NSW, Australia
[2] Pharmafood Inst, Kyoto, Japan
关键词
diabetes; PPAR; Punica granatum Linn;
D O I
10.1111/j.1463-1326.2007.00708.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
PPARs are transcription factors belonging to the superfamily of nuclear receptors. PPAR-alpha is involved in the regulation of fatty acid (FA) uptake and oxidation, inflammation and vascular function, while PPAR-gamma participates in FA uptake and storage, glucose homeostasis and inflammation. The PPARs are thus major regulators of lipid and glucose metabolism. Synthetic PPAR-alpha or PPAR-gamma agonists have been widely used in the treatment of dyslipidaemia, hyperglycaemia and their complications. However, they are associated with an incidence of adverse events. Given the favourable metabolic effects of both PPAR-alpha and PPAR-gamma activators, as well as their potential to modulate vascular disease, combined PPAR-alpha/-gamma activation has recently emerged as a promising concept, leading to the development of mixed PPAR-alpha/-gamma activators. However, some major side effects associated with the synthetic dual activators have been reported. It is unclear whether this is a specific effect of the particular synthetic compounds or a class effect. To date, a medication that may combine the beneficial metabolic effects of PPAR-alpha and PPAR-gamma activation with fewer undesirable side effects has not been successfully developed. Pomegranate plant parts are used traditionally for the treatment of various disorders. However, only pomegranate flower has been prescribed in Unani and Ayurvedic medicines for the treatment of diabetes. This review provides a new understanding of the dual PPAR-alpha/-gamma activator properties of pomegranate flower in the potential treatment of diabetes and its associated complications.
引用
收藏
页码:10 / 17
页数:8
相关论文
共 65 条
[1]   Cardiac function and metabolism in Type 2 diabetic mice after treatment with BM 17.0744, a novel PPAR-α activator [J].
Aasum, E ;
Belke, DD ;
Severson, DL ;
Riemersma, RA ;
Cooper, M ;
Andreassen, M ;
Larsen, TS .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 283 (03) :H949-H957
[2]   Glucose transport in the heart [J].
Abel, ED .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2004, 9 :201-215
[3]   Effects of oleanane-type triterpenoids from fabaceous plants on the expression of ICAM-1 [J].
Ahn, KS ;
Kim, JH ;
Oh, SR ;
Min, BS ;
Kinjo, J ;
Lee, HK .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2002, 25 (08) :1105-1107
[4]   Gallic acid antagonizes P-selectin-mediated platelet-leukocyte interactions - Implications for the French paradox [J].
Appeldoorn, CCM ;
Bonnefoy, A ;
Lutters, BCH ;
Daenens, K ;
van Berkel, TJC ;
Hoylaerts, MF ;
Biessen, EAL .
CIRCULATION, 2005, 111 (01) :106-112
[5]   Pharmacotherapy for dyslipidaemia - current therapies and future agents [J].
Bays, H ;
Stein, EA .
EXPERT OPINION ON PHARMACOTHERAPY, 2003, 4 (11) :1901-1938
[6]   The role of nuclear factor-kappa B in cytokine gene regulation [J].
Blackwell, TS ;
Christman, JW .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 17 (01) :3-9
[7]  
Brewer HB, 1999, AM J CARDIOL, V83, p3F
[8]   High glucose-induced, endothelin-dependent fibronectin synthesis is mediated via NF-κB and AP-1 [J].
Chen, SL ;
Mukherjee, S ;
Chakraborty, C ;
Chakrabarti, S .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2003, 284 (02) :C263-C272
[9]   Nuclear factor κB:: a pivotal role in the systemic inflammatory response syndrome and new target for therapy [J].
Christman, JW ;
Lancaster, LH ;
Blackwell, TS .
INTENSIVE CARE MEDICINE, 1998, 24 (11) :1131-1138
[10]   Induction of IκBα expression as a mechanism contributing to the anti-inflammatory activities of peroxisome proliferator-activated receptor-α activators [J].
Delerive, P ;
Gervois, P ;
Fruchart, JC ;
Staels, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (47) :36703-36707