TY - JOUR
T1 - Temporal nature of insulin binding and insulin-stimulated glucose metabolism in isolated swine adipocytes.
AU - Chung, C. S.
AU - Meserole, V. K.
AU - Etherton, T. D.
PY - 1983/1
Y1 - 1983/1
N2 - Insulin binding and insulin-stimulated glucose metabolism were measured in swine adipocytes isolated from adipose tissue obtained by biopsy on 4 successive days. These characteristics were also measured in adipose tissue obtained on the 5th d immediately after exsanguination. Binding of 125I-insulin was measured at three different concentrations of unlabeled insulin (0, 1, 100 ng/ml) on each day. Specific binding (pg bound . 2 X 10(5) adipocytes-1 X 90 min-1) was not different (P greater than .05) for each insulin concentration among the 5 d. Specifically bound insulin increased (P less than .05) with increasing insulin concentration. The effects of insulin (0, 1, 100 ng/ml) on glucose oxidation and glucose conversion to lipid were also examined in biopsy (B) and postmortem (PM) adipocytes. For a respective insulin concentration, there was no difference in glucose oxidation or lipid synthesis over the 5-d (four B, one PM) sampling period. Lipid synthesis was stimulated by the presence of insulin (P less than .05; 1 and 100 ng/ml) when compared with basal incubations; however, glucose oxidation was unaffected by the presence of insulin. There was no difference in lipid synthetic rates between 1 and 100 ng/ml of insulin. The responsiveness of glucose oxidation and lipid synthesis to insulin in PM samples was identical to that for adipocytes from B samples. These results indicate: 1) that glucose metabolism and insulin binding to adipocytes isolated from swine adipose tissue obtained by biopsy did not differ from that in tissue samples obtained shortly after death and 2) that insulin-stimulated glucose metabolism and insulin binding did not fluctuate appreciably over a 5-d period when adipose tissue was obtained at the same time each day.
AB - Insulin binding and insulin-stimulated glucose metabolism were measured in swine adipocytes isolated from adipose tissue obtained by biopsy on 4 successive days. These characteristics were also measured in adipose tissue obtained on the 5th d immediately after exsanguination. Binding of 125I-insulin was measured at three different concentrations of unlabeled insulin (0, 1, 100 ng/ml) on each day. Specific binding (pg bound . 2 X 10(5) adipocytes-1 X 90 min-1) was not different (P greater than .05) for each insulin concentration among the 5 d. Specifically bound insulin increased (P less than .05) with increasing insulin concentration. The effects of insulin (0, 1, 100 ng/ml) on glucose oxidation and glucose conversion to lipid were also examined in biopsy (B) and postmortem (PM) adipocytes. For a respective insulin concentration, there was no difference in glucose oxidation or lipid synthesis over the 5-d (four B, one PM) sampling period. Lipid synthesis was stimulated by the presence of insulin (P less than .05; 1 and 100 ng/ml) when compared with basal incubations; however, glucose oxidation was unaffected by the presence of insulin. There was no difference in lipid synthetic rates between 1 and 100 ng/ml of insulin. The responsiveness of glucose oxidation and lipid synthesis to insulin in PM samples was identical to that for adipocytes from B samples. These results indicate: 1) that glucose metabolism and insulin binding to adipocytes isolated from swine adipose tissue obtained by biopsy did not differ from that in tissue samples obtained shortly after death and 2) that insulin-stimulated glucose metabolism and insulin binding did not fluctuate appreciably over a 5-d period when adipose tissue was obtained at the same time each day.
UR - http://www.scopus.com/inward/record.url?scp=0020673909&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0020673909&partnerID=8YFLogxK
U2 - 10.2527/jas1983.56158x
DO - 10.2527/jas1983.56158x
M3 - Article
C2 - 6337986
AN - SCOPUS:0020673909
SN - 0021-8812
VL - 56
SP - 58
EP - 63
JO - Journal of animal science
JF - Journal of animal science
IS - 1
ER -