| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| H Gäbel, H Brynger, L Heding, J Säve-Söderbergh, N Wedel, K Lundhol. Pancreas transplantation in streptozotocin-diabetic juvenile pigs. Evaluation of function among duct-ligated, duct-occluded, and nonligated allografts. Transplantation. vol 36. issue 6. 1984-02-14. PMID:6362137. |
normal glucose tolerance in transplanted pigs was associated with elevated levels of normal insulin and c-peptide in peripheral blood, concomitant with low levels of proinsulin. |
1984-02-14 |
2023-08-12 |
Not clear |
| G S Spencer, G J Garssen, B Colenbrander, A A Macdonald, M M Bever. Glucose, growth hormone, somatomedin, cortisol and ACTH changes in the plasma of unanaesthetised pig foetuses following intravenous insulin administration in utero. Acta endocrinologica. vol 104. issue 2. 1983-12-17. PMID:6314725. |
insulin tolerance tests were carried out in chronically catheterised foetal pigs. |
1983-12-17 |
2023-08-12 |
Not clear |
| M Yajima, T Okamoto, S Kurokawa, A Itoh, A Terashima, M U. Species differences in actions of islet-activating protein, pertussis toxin. Japanese journal of pharmacology. vol 33. issue 3. 1983-11-23. PMID:6353019. |
the ability of iap to cause potentiation of insulin secretory responses and promotion of leukocytosis was studied in six animal species (hamsters, rats, guinea pigs, rabbits, dogs and monkeys). |
1983-11-23 |
2023-08-12 |
rat |
| Y Shechter, D Elias, R Maron, I R Cohe. Mice immunized to insulin develop antibody to the insulin receptor. Journal of cellular biochemistry. vol 21. issue 2. 1983-10-08. PMID:6350327. |
bioactivity could be blocked efficiently by insulin antibodies from guinea pigs and from mice. |
1983-10-08 |
2023-08-12 |
mouse |
| J L Rosenzweig, D Le Roith, M A Lesniak, I MacIntyre, W H Sawyer, J Rot. Two distinct insulins in the guinea pig: the broad relevance of these findings to evolution of peptide hormones. Federation proceedings. vol 42. issue 9. 1983-07-29. PMID:6343124. |
in this paper we use the published data of others as well as our own recent data to question the widespread assumption that the gene for guinea pig insulin mutated rapidly after the divergence of guinea pigs from the main line of rodent evolution. |
1983-07-29 |
2023-08-12 |
Not clear |
| J L Rosenzweig, D Le Roith, M A Lesniak, I MacIntyre, W H Sawyer, J Rot. Two distinct insulins in the guinea pig: the broad relevance of these findings to evolution of peptide hormones. Federation proceedings. vol 42. issue 9. 1983-07-29. PMID:6343124. |
we suggest that instead guinea pigs may have two pairs of alleles, one for typical guinea pig insulin, which is expressed in its pancreatic beta cells, and the other for a more typical mammalian insulin (designated rat/pork-type insulin), which is expressed in extrapancreatic cells. |
1983-07-29 |
2023-08-12 |
Not clear |
| M J Müller, U Paschen, H J Seit. Thyroid hormone regulation of glucose homeostasis in the miniature pig. Endocrinology. vol 112. issue 6. 1983-07-08. PMID:6343057. |
during starvation serum insulin showed a similar decrease in all thyroid states; glucagon increased in euthyroid and hypothyroid pigs, although it was already elevated in the hyperthyroid fed state. |
1983-07-08 |
2023-08-12 |
Not clear |
| T R Kasser, G J Hausman, D R Campion, R J Marti. Lipogenesis and pancreatic insulin release in fetal pigs. Journal of animal science. vol 56. issue 3. 1983-06-17. PMID:6341347. |
lipogenesis and pancreatic insulin release in fetal pigs. |
1983-06-17 |
2023-08-12 |
Not clear |
| T R Kasser, G J Hausman, D R Campion, R J Marti. Lipogenesis and pancreatic insulin release in fetal pigs. Journal of animal science. vol 56. issue 3. 1983-06-17. PMID:6341347. |
body composition, liver and adipose lipogenesis, and pancreatic insulin release were examined in intact and decapitated fetal pigs on d 110 of gestation. |
1983-06-17 |
2023-08-12 |
Not clear |
| G A Dos Reis, E M Shevac. Antigen-presenting cells from nonresponder strain 2 guinea pigs are fully competent to present bovine insulin B chain to responder strain 13 T cells. Evidence against a determinant selection model and in favor of a clonal deletion model of immune response gene function. The Journal of experimental medicine. vol 157. issue 4. 1983-05-27. PMID:6187889. |
antigen-presenting cells from nonresponder strain 2 guinea pigs are fully competent to present bovine insulin b chain to responder strain 13 t cells. |
1983-05-27 |
2023-08-12 |
cattle |
| G A Dos Reis, E M Shevac. Antigen-presenting cells from nonresponder strain 2 guinea pigs are fully competent to present bovine insulin B chain to responder strain 13 T cells. Evidence against a determinant selection model and in favor of a clonal deletion model of immune response gene function. The Journal of experimental medicine. vol 157. issue 4. 1983-05-27. PMID:6187889. |
strain 2 macrophages were found to be fully competent to present bovine insulin b chain to strain 13 t cells despite the fact that strain 2 guinea pigs are normally totally unresponsive to this antigen. |
1983-05-27 |
2023-08-12 |
cattle |
| R W Phillips, L M Panepinto, R Spangler, N Westmorelan. Yucatan miniature swine as a model for the study of human diabetes mellitus. Diabetes. vol 31. issue Suppl 1 Pt 2. 1983-04-07. PMID:6761193. |
in two pigs the decreased peripheral insulin resulted from increased hepatic uptake of insulin. |
1983-04-07 |
2023-08-12 |
human |
| K A Houpt, B A Baldwin, T R Houpt, F Hill. Humoral and cardiovascular responses to feeding in pigs. The American journal of physiology. vol 244. issue 2. 1983-03-17. PMID:6337512. |
in young pigs, allowed to feed after various periods of food deprivation, the changes in plasma levels of insulin, glucose, and corticosteroids were measured. |
1983-03-17 |
2023-08-12 |
Not clear |
| K A Houpt, B A Baldwin, T R Houpt, F Hill. Humoral and cardiovascular responses to feeding in pigs. The American journal of physiology. vol 244. issue 2. 1983-03-17. PMID:6337512. |
in pigs deprived of food for 17 h there was a marked rise in insulin from 15 +/- 1 to 91 +/- 10 microu/ml and glucose from 94 +/- 2 to 112 +/- 4 mg/dl when feeding began, while the corticosteroid levels were reduced from 48 +/- 8 to 29 +/- 9 ng/ml. |
1983-03-17 |
2023-08-12 |
Not clear |
| K A Houpt, B A Baldwin, T R Houpt, F Hill. Humoral and cardiovascular responses to feeding in pigs. The American journal of physiology. vol 244. issue 2. 1983-03-17. PMID:6337512. |
evidence for a cephalic phase of insulin secretion was seen in 17-h fasted pigs. |
1983-03-17 |
2023-08-12 |
Not clear |
| K A Houpt, B A Baldwin, T R Houpt, F Hill. Humoral and cardiovascular responses to feeding in pigs. The American journal of physiology. vol 244. issue 2. 1983-03-17. PMID:6337512. |
in pigs fed ad libitum there were no significant changes in the levels of insulin, glucose, or corticosteroids. |
1983-03-17 |
2023-08-12 |
Not clear |
| H J Mersmann, W G Pond, J T Ye. Plasma glucose, insulin and lipids during growth of genetically lean and obese swine. Growth. vol 46. issue 3. 1983-02-25. PMID:6757063. |
female pigs were selected at birth from litters of genetically lean and obese and contemporary commercial-type pigs to quantify the biweekly changes in fasting concentrations of plasma glucose, immunoreactive insulin, triglyceride and cholesterol during the growing period (birth to 22 weeks of age). |
1983-02-25 |
2023-08-12 |
Not clear |
| H J Mersmann, W G Pond, J T Ye. Plasma glucose, insulin and lipids during growth of genetically lean and obese swine. Growth. vol 46. issue 3. 1983-02-25. PMID:6757063. |
the genetically lean pigs had lower insulin and triglyceride levels, especially at older ages. |
1983-02-25 |
2023-08-12 |
Not clear |
| H J Mersmann, W G Pond, J T Ye. Plasma glucose, insulin and lipids during growth of genetically lean and obese swine. Growth. vol 46. issue 3. 1983-02-25. PMID:6757063. |
it is concluded that these genetically obese pigs selected for fatness over many generations do not manifest their propensity to obesity through modifications in circulating glucose, insulin, triglyceride or cholesterol. |
1983-02-25 |
2023-08-12 |
Not clear |
| C G Ostenson, I Swenne, P R Flatt, P O Berggre. Insulin antibody production in guinea pigs is accompanied by disturbances in pancreatic islet morphology and glucagon secretion. Diabete & metabolisme. vol 8. issue 3. 1983-01-27. PMID:6754495. |
insulin antibody production in guinea pigs is accompanied by disturbances in pancreatic islet morphology and glucagon secretion. |
1983-01-27 |
2023-08-12 |
Not clear |