The therapeutic potential of insulin-mimetic vanadium complexes

被引:44
作者
Sakurai, H [1 ]
Yasui, H [1 ]
Adachi, Y [1 ]
机构
[1] Kyoto Pharmaceut Univ, Dept Analyt & Bioinorgan Chem, Yamashina Ku, Kyoto 6078414, Japan
关键词
adipocytes; blood circulation monitoring-EPR; blood glucose; coordination mode; diabetes mellitus; insulin-mimetic activity; structure-activity relationship; vanadyl(IV) complexes;
D O I
10.1517/13543784.12.7.1189
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Throughout the world, the number of patients suffering from diabetes mellitus (DM) is increasing on a daily basis, probably due to change in lifestyle. DM is mainly classified as either insulin-dependent Type 1 or non-insulin-dependent Type 2, according to the definition of WHO. To treat DM, which has many severe complications, several types of insulin preparations and synthetic drugs for Type 1 and Type 2 DM, respectively, have been developed and are in clinical use. However, there are several problems concerning the insulin preparations and synthetic drugs, such as physical and mental pain due to daily insulin injections and defects involving side effects, respectively. Consequently, a new class of therapeutic agents is anticipated. For this purpose, vanadium-containing complexes are expected to treat or improve both types of DM by using unique characteristics of the transition metal. In this article, the current state of research on insulin-mimetic vanadium complexes are reviewed, with special focus on the paramagnetic vanadyl (+4 oxidation state of vanadium) complexes with different coordination modes. To analyse the blood glucose-lowering effects of the vanadyl complexes, new results on the organ distribution and pharmacokinetic analysis of the vanadyl state in the blood of rats are also described.
引用
收藏
页码:1189 / 1203
页数:15
相关论文
共 77 条
[11]  
DUNAI N, 1997, J CLIN BIOCHEM NUTR, V22, P31
[12]   Modulation of insulin action by vanadate: Evidence of a role for phosphotyrosine phosphatase activity to alter cellular signaling [J].
Fantus, IG ;
Deragon, G ;
Lai, R ;
Tang, S .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1995, 153 (1-2) :103-112
[13]   Pharmacokinetic study on gastrointestinal absorption of insulinomimetic vanadyl complexes in rats by ESR spectroscopy [J].
Fugono, J ;
Yasui, H ;
Sakurai, H .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2001, 53 (09) :1247-1255
[14]   Enteric-coating capsulation of insulinomimetic vanadyl sulfate enhances bioavailability of vanadyl species in rats [J].
Fugono, J ;
Yasui, H ;
Sakurai, H .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2002, 54 (05) :611-615
[15]  
Fujimoto S, 1997, J CLIN BIOCHEM NUTR, V23, P113
[16]  
Fujisawa Y, 1999, CHEM PHARM BULL, V47, P1668, DOI 10.1248/cpb.47.1668
[17]   DETECTION OF VANADYL-NITROGEN INTERACTION IN ORGANS OF THE VANADYL-TREATED RAT - ELECTRON-SPIN ECHO ENVELOPE MODULATION STUDY [J].
FUKUI, K ;
OHYANISHIGUCHI, H ;
NAKAI, M ;
SAKURAI, H ;
KAMADA, H .
FEBS LETTERS, 1995, 368 (01) :31-35
[18]   In vivo coordination structural changes of a potent insulin-mimetic agent, bis(picolinato) oxovanadium(IV), studied by electron spin-echo envelope modulation spectroscopy [J].
Fukui, K ;
Fujisawa, Y ;
Ohya-Nishiguchi, H ;
Kamada, H ;
Sakurai, H .
JOURNAL OF INORGANIC BIOCHEMISTRY, 1999, 77 (3-4) :215-224
[19]   METABOLIC EFFECTS OF SODIUM METAVANADATE IN HUMANS WITH INSULIN-DEPENDENT AND NONINSULIN-DEPENDENT - DIABETES-MELLITUS IN-VIVO AND IN-VITRO STUDIES [J].
GOLDFINE, AB ;
SIMONSON, DC ;
FOLLI, F ;
PATTI, ME ;
KAHN, CR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (11) :3311-3320
[20]   L-glutamic acid γ-monohydroxamate -: A potentiator of vanadium-evoked glucose metabolism in vitro and in vivo [J].
Goldwaser, I ;
Li, JP ;
Gershonov, E ;
Armoni, M ;
Karnieli, E ;
Fridkin, M ;
Shechter, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (37) :26617-26624