Browse > Article
http://dx.doi.org/10.5713/ajas.2002.1210

Effects of Gut Extract Protein and Insulin on Glucose Uptake and GLUT 1 Expression in HC 11 Mouse Mammary Epithelial Cells  

Myung, K.H. (Department of Animal Science, Chonnam National University)
Ahn, B.J. (Department of Animal Science, Chonnam National University)
Publication Information
Asian-Australasian Journal of Animal Sciences / v.15, no.8, 2002 , pp. 1210-1214 More about this Journal
Abstract
The large and rapid changes of glucose utilization in lactating mammary tissue in response to changes in nutritional state must be largely related by external signal of insulin. This also must be related with the quantity and composition of the diet in vivo. To characterize the mode of gut extract protein with insulin, in vitro experiment was conducted with HC11 cells. The gut extract protein has not only the same effect as insulin alone but also the synergistic effect with insulin in 2-Deoxy[3H] glucose uptake. Although the gut extract did not modulates glucose uptake via increasing the rate of translation of the GLUT1 protein, northern blot analysis indicated that the gut extract protein increased the expression of GLUT1 mRNA by a threefold and also there was a dose-dependent increase in the expression of GLUT1 mRNA. The gut extract protein is therefore shown to be capable of modulating glucose uptake by transcription level with insulin in HC 11 cells.
Keywords
Gut Extract Protein; Glucose Uptake; HC11; GLUT1;
Citations & Related Records

Times Cited By Web Of Science : 0  (Related Records In Web of Science)
Times Cited By SCOPUS : 1
연도 인용수 순위
1 Bennett, B. L. 1995. Glucose transporter gene expression in mammary tissue. Ph. D. Thesis, Univ.of Otago, New Zealand.
2 Bernier, M. D. M. Laird and M. D. Lane. 1988. Effects of vanadate on the cellular accumulation of pp15, an apparant product of insulin receptor tyrosine kinase action. J. Biol. Chem. 263:13626-13634.
3 Cesarone, C. F., C. Bolognesi and M. Peaker. 1980. Improved microflurorometric DNA determination n biological material using 33258 Hoescht. Anal. Boichem. 100:188-197.   DOI   ScienceOn
4 Wang, Y. H. K. Kole, C. Montrose-Rafizadeh, R. Perfetti, M. Bernier and J. M. Egan. 1977. Regulation of glucose transporters and hexose uptake in 3T3-L1 adipocyte:glucogan-like peptide-1 and insulin interactions. J. Mol. Endocrinol. 19:241-248.   DOI   ScienceOn
5 Chomozynski, P. and N. Sacchi. 1987. Single-step method of RNA isolation by acid guanidium thiocyanate-phenolcholoform extraction. Anal. Biochem. 162:156-159.
6 SAS Institute Inc. 1997. SAS Users Guide: Release 6.07. Cary, North Carolina, SAS Institute.
7 Doppler, W., B. Groner and R. K. Ball. 1989. Prolactin and glucocorticoid hormones synergistically induce expression of transfected rat beta-casein gene promoter constructs in a mammary epithelial cell line. Proc. Natl. Acad. Sci. USA. 86:104-108.   DOI   ScienceOn
8 Laemmli, U. K. 1970. Cleveage of structural proteins during the assembled of the head of bacteriophage T4. Nature 227:680-685.   DOI   ScienceOn
9 Williamson, D. H., M. R. Munray, R. G. Jones, R. G., A. F. C. Roberts and A. J. Ramsey. 1983. Adv. Enzyme Regul. 21:135-144.   DOI   ScienceOn
10 Robinson, A. M., J. R. Girald and D. H. Williamson. 1978. Utlization of D-3-hydroxy[3-14C]butyrate for lipogenesis in vivo in lactating rat mammary gland. Briochem. J. 176:343-346.
11 Prosser, C. G. 1988. Mechanism of the decrease in hexose transpor by mouse mammary epitherial cells caused by fasting. Biochem. J. 249:149-154.
12 Page, T. 1989. Evidence for the involvement of a gastrointestinal peptide in the regulation of glucose uptake in the mammary gland of the lactating rat. Biochem. J. 258:39-643.
13 Page, T. and N. J. Kuhn. 1986. Arteriovenous glucose differences across the mammary gland of the fed, starved, and re-fed lactating rat. Biochem. J. 239:269-274.
14 Linzell, J. L. 1967. The effect of very frequent milking and of oxytocin on the yield and composition of milk in fed and fasted goats. J. Physiol. 190:333-346.   DOI   PUBMED