Determination of the L-ascorbic acid requirements in Wister osteogenic disorder Shionogi rats for prolonged carcinogenesis experiments

被引:8
作者
Chan, SWY
Reade, PC
机构
[1] Oral Medicine and Surgery Research Unit, School of Dental Science, University of Melbourne
[2] Oral Medicine and Surgery Research Unit, School of Dental Science, Melbourne, Vic. 3000
关键词
plasma L-ascorbic acid requirement; Wistar osteogenic disorder rat; carcinogenesis;
D O I
10.1258/002367796780739826
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Wistar Shionogi rats of the (od/od) substrain with the osteogenic disorder are unable to synthesize L-ascorbic acid (L-AA) and appear to be an appropriate animal model for studying the effect of L-AA in carcinogenesis. To determine the minimal L-AA requirements of these animals for prolonged survival in a satisfactory physical condition during experimentation, four concentrations of L-AA (0.33 g/l, 0.67 g/l, 1.67 g/l and 3.33 g/l) were administered via drinking water to four groups of animals (n=2). Their water intake per cage was recorded three times weekly and the plasma L-AA levels were determined at the start, after 2, 4, 8 and 12 weeks and at the termination of the experiment. To simulate the procedures to be undertaken in oral mucosal carcinogenesis experiments, the animals were gently restrained and a designated amount of sterile NaCl was applied to the palatal mucosa three times a week for 26 weeks. The L-AA supplement group with the lowest concentration (0.33 g/l L-AA) achieved mean plasma levels of 7 +/- 1.38 mu M, approximately one-eighth that of the normal level (mean plasma L-AA level in outbred Wistar rats was found to be 58 +/- 3 mu M) whilst those in the higher supplement group (3.33 g/l L-AA) achieved a mean of 18 +/- 1.25 mu M. All of the animals employed in the present study survived for 26 weeks and showed no clinical signs of L-AA. deficiency during this period.
引用
收藏
页码:337 / 346
页数:10
相关论文
共 39 条
[1]   SEVERE HYPOVITAMINOSIS-C IN LUNG-CANCER PATIENTS - THE UTILIZATION OF VITAMIN-C IN SURGICAL REPAIR AND LYMPHOCYTE-RELATED HOST-RESISTANCE [J].
ANTHONY, HM ;
SCHORAH, CJ .
BRITISH JOURNAL OF CANCER, 1982, 46 (03) :354-367
[2]   METABOLISM OF ASCORBIC-ACID AND ASCORBIC-2-SULFATE IN MAN AND SUBHUMAN PRIMATE [J].
BAKER, EM ;
HALVER, JE ;
JOHNSEN, DO ;
JOYCE, BE ;
KNIGHT, MK ;
TOLBERT, BM .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1975, 258 (SEP30) :72-80
[3]  
BENEDICT WF, 1982, MOL INTERRELATIONS N, P351
[4]   VITAMIN-C AND CANCER PREVENTION - THE EPIDEMIOLOGIC EVIDENCE [J].
BLOCK, G .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1991, 53 (01) :S270-S282
[5]   SYNTHESIS AND SOME MAJOR FUNCTIONS OF VITAMIN-C IN ANIMALS [J].
CHATTERJEE, IB ;
MAJUMDER, AK ;
NANDI, BK ;
SUBRAMANIAN, N .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1975, 258 (SEP30) :24-47
[6]  
CLEMETSON CAB, 1989, VITAMIN C, V1
[7]  
CLEMETSON CAB, 1989, VITAMIN C, V3
[8]  
CLEMETSON CAB, 1989, VITAMIN C, V2
[9]  
Cooke JR, 1981, VITAMIN C, P167
[10]  
CURTIN CO, 1955, J BIOL CHEM, V216, P539