In vivo assessment of toxicity and pharmacokinetics of methylglyoxal - Augmentation of the curative effect of methylglyoxal on cancer-bearing mice by ascorbic acid and creatine

被引:60
作者
Ghosh, M
Talukdar, D
Ghosh, S
Bhattacharyya, N
Ray, M [1 ]
Ray, S
机构
[1] Indian Assoc Cultivat Sci, Dept Biol Chem, Kolkata 700032, W Bengal, India
[2] Univ Calcutta, Coll Sci, Dept Biochem, Kolkata 700019, W Bengal, India
关键词
methylglyoxal; ascorbic acid; creatine; toxicity; pharmacokinetics; cancer treatment;
D O I
10.1016/j.taap.2005.07.003
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Previous in vivo studies from several laboratories had shown remarkable curative effect of methylglyoxal on cancer-bearing animals. In contrast, most of the recent in vitro studies have assigned a toxic role for methylglyoxal. The present study was initiated with the objective to resolve whether methylglyoxal is truly toxic in vivo and to reassess its therapeutic potential. Four species of animals, both rodent and non-rodent, were treated with different doses of methylglyoxal through oral, subcutaneous and intravenous routes. Acute (treatment for only I day) toxicity tests had been done with mouse and rat. These animals received 2, 1 and 0.3 a of methylglyoxal/kg of body weight in a day through oral, subcutaneous and intravenous routes respectively. Chronic (treatment for around a month) toxicity test had been done with mouse, rat, rabbit and dog. Mouse, rat and dog received 1, 0.3 and 0.1 g of methylglyoxal/kg of body weight in a day through oral, subcutaneous and intravenous routes respectively. Rabbit received 0.55, 0.3 and 0.1 g of methylglyoxal/kg of body weight in a day through oral, subcutaneous and intravenous routes respectively. It had been observed that rnethylglyoxal had no deleterious effect on the physical and behavioral pattern of the treated animals. Fertility and teratogenecity studies were done with rats that were subjected to chronic toxicity tests. It had been observed that these animals produced healthy litters indicating no damage of the reproductive systems as well as no deleterious effect on the offspring. Studies on several biochemical and hematological parameters of methylglyoxal-treated rats and dogs and histological studies of several organs of methylglyoxal-treated mouse were performed. These studies indicated that methylglyoxal had no apparent deleterious effect on some vital organs of these animals. A detailed pharmacokinetic study was done with Mouse after oral administration of methylglyoxal. The effect of methylglyoxal alone and in combination with creatine and ascorbic acid on cancer-bearing animals had been investigated by measuring the increase in life span and tumor cell growth inhibition. The results indicated that anticancer effect of rnethylglyoxal was significantly augmented by ascorbic acid and further augmented by ascorbic acid and creatine. Nearly 80% of the animals treated with methylglyoxal plus ascorbic acid plus creatine were completely cured and devoid of any malignant cells within the peritoneal cavity. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:45 / 58
页数:14
相关论文
共 37 条
[1]
Inhibition of gastric mucosal damage by methylglyoxal pretreatment in rats [J].
Al-Shabanah, OA ;
Qureshi, S ;
Al-Harbi, MM ;
Al-Bekairi, AM ;
Al-Gharably, NM ;
Raza, M .
FOOD AND CHEMICAL TOXICOLOGY, 2000, 38 (07) :577-584
[2]
APPLE MA, 1968, CANCER CHEMOTH REP 1, V52, P687
[3]
APPLE MA, 1967, CANC CHEMOTHER REP, V521, P455
[4]
BENET LZ, 1996, PHARMACOL BASIS THER, P3
[5]
Selective inhibition of mitochondrial respiration and glycolysis in human leukaemic leucocytes by methylglyoxal [J].
Biswas, S ;
Ray, M ;
Misra, S ;
Dutta, DP ;
Ray, S .
BIOCHEMICAL JOURNAL, 1997, 323 :343-348
[6]
Curcumin inhibits ROS formation and apoptosis in methylglyoxal-treated human hepatoma G2 cells [J].
Chan, WH ;
Wu, HJ ;
Hsuuw, YD .
ROLE OF THE MITOCHONDRIA IN HUMAN AGING AND DISEASE: FROM GENES TO CELL SIGNALING, 2005, 1042 :372-378
[7]
Methylglyoxal-induced nitric oxide and peroxynitrite production in vascular smooth muscle cells [J].
Chang, TJ ;
Wang, R ;
Wu, LY .
FREE RADICAL BIOLOGY AND MEDICINE, 2005, 38 (02) :286-293
[8]
Conroy P.J., 1979, CIBA F S, V67, P271
[9]
Cooper R A, 1975, Methods Enzymol, V41, P502
[10]
Methylglyoxal assay in cells as 2-methylquinoxaline using 1,2-diaminobenzene as derivatizing reagent [J].
Cordeiro, C ;
Freire, AF .
ANALYTICAL BIOCHEMISTRY, 1996, 234 (02) :221-224