Modulation of proinsulin messenger RNA after partial pancreatectomy in rats. Relationships to glucose homeostasis.

These studies of partial pancreatectomy assess pancreatic proinsulin messenger RNA (mRNA) levels as an index of in vivo insulin biosynthesis, and show relationships to glucose homeostasis. Rats were subjected to sham operation, 50% pancreatectomy (Px), or 90% Px, and were examined after 1, 3, or 14 wk. Proinsulin mRNA was measured by dot hybridization to complementary DNA. After 50% Px there was a nearly complete adaptation of proinsulin mRNA. After 90% Px a marked increase of proinsulin mRNA occurred, but it was insufficient and it was not maintained with time. The deficit in insulin production is related to development of hyperglycemia. Sham-operated controls showed no worsening of fasting or fed blood glucose or of intraperitoneal glucose tolerance within the period of observation. Total proinsulin mRNA and pancreatic insulin content rose in proportion to body weight. 50% Px produced no change from controls in body weight or blood glucose. The concentration of proinsulin mRNA in the 50% pancreatic remnant paralleled that of controls after 1 and 3 wk, but then increased after 14 wk, such that total proinsulin mRNA approached control levels. This adaptive response was reflected by changes in serum insulin, but not by pancreatic insulin content, which was only 30% of control after 14 wk. Intraperitoneal glucose tolerance was impaired mildly, and did not worsen with time after pancreatectomy. 90% Px led to elevated fed blood glucose and reduced serum insulin after 3 wk, and fasting hyperglycemia was seen after 14 wk. Proinsulin mRNA concentration in the 10% pancreatic remnant showed an adaptive increase after 1 and 3 wk, such that total proinsulin mRNA reached 40% of control. After 14 wk, however, remnant proinsulin mRNA concentration was no longer increased; total proinsulin mRNA and pancreatic insulin content were severely reduced. Intraperitoneal glucose tolerance was impaired more dramatically than with the 50% Px animals, and worsened with time after operation. These observations indicate ability to increase proinsulin mRNA levels as an adaptation to pancreatectomy. Insufficiency of this adaptation is associated with the development of hyperglycemia, and the loss of this adaptation correlates with a worsening of glucose tolerance.

[1]  M. Permutt,et al.  Impaired Insulin Biosynthetic Capacity in a Rat Model for Non-insulin-dependent Diabetes: Studies with Dexamethasone , 1985, Diabetes.

[2]  J. Dagorn,et al.  Regulation of amylase messenger RNA concentration in rat pancreas by food content. , 1984, The EMBO journal.

[3]  R. Gleason,et al.  Differential Sensitivity to β-Cell Secretagogues in “Early,” Type I Diabetes Mellitus , 1984, Diabetes.

[4]  M. Permutt,et al.  An in vivo analysis of pancreatic protein and insulin biosynthesis in a rat model for non-insulin-dependent diabetes. , 1984, The Journal of clinical investigation.

[5]  A. Andrén-sandberg,et al.  Factors Influencing Survival After Total Pancreatectomy in Patients with Pancreatic Cancer , 1983, Annals of surgery.

[6]  D. Granner,et al.  Inhibition of transcription of the phosphoenolpyruvate carboxykinase gene by insulin , 1983, Nature.

[7]  M. Permutt,et al.  Insulin Gene Expression in the Developing Rat Pancreas , 1983, Diabetes.

[8]  S. Bonner-Weir,et al.  Partial pancreatectomy in the rat and subsequent defect in glucose-induced insulin release. , 1983, The Journal of clinical investigation.

[9]  P. Thomas,et al.  Hybridization of denatured RNA transferred or dotted nitrocellulose paper. , 1983, Methods in enzymology.

[10]  G. Weir Non-insulin-dependent diabetes mellitus: interplay between B-cell inadequacy and insulin resistance. , 1982, The American journal of medicine.

[11]  L. Orci,et al.  Quantitation of Endocrine Cell Content in the Pancreas of Nondiabetic and Diabetic Humans , 1982, Diabetes.

[12]  M. Permutt,et al.  Effects of Glucose on Proinsulin Messenger RNA in Rats In Vivo , 1982, Diabetes.

[13]  S. Chan,et al.  Direct effect of glucose on the preproinsulin mRNA level in isolated pancreatic islets. , 1982, Biochemical and biophysical research communications.

[14]  P. Halban,et al.  Functional differences between rat islets of ventral and dorsal pancreatic origin. , 1982, The Journal of clinical investigation.

[15]  S. Bonner-Weir,et al.  Islet Secretion in a New Experimental Model for Non-insulin-dependent Diabetes , 1981, Diabetes.

[16]  M. Permutt,et al.  The effects of fasting and feeding on preproinsulin messenger RNA in rats. , 1981, The Journal of clinical investigation.

[17]  P. Lecompte,et al.  The pancreatic islets in diabetes. , 1981, The American journal of medicine.

[18]  J. Najarian,et al.  Living-related donor segmental pancreatectomy for transplantation. , 1980, Transplantation proceedings.

[19]  W. Rutter,et al.  Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. , 1979, Biochemistry.

[20]  Tohru Takahashi,et al.  Differential volumetry of A, B and D cells in the pancreatic islets of diabetic and nondiabetic subjects. , 1979, The Tohoku journal of experimental medicine.

[21]  W. Rutter,et al.  Isolation and characterization of a cloned rat insulin gene , 1979, Cell.

[22]  W. Rutter,et al.  Synthesis and accumulation of proinsulin and insulin during development of the embryonic rat pancreas. , 1979, Endocrinology.

[23]  G. Reaven,et al.  Effect of age on glucose-stimulated insulin release by the beta-cell of the rat. , 1979, The Journal of clinical investigation.

[24]  G R Stark,et al.  Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[25]  J. Taylor,et al.  Correlation of albumin production rates and albumin mRNA levels in livers of normal, diabetic, and insulin-treated diabetic rats. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[26]  H. Okamoto,et al.  Glucose stimulation of the proinsulin synthesis in isolated pancreatic islets without increasing amount of proinsulin mRNA , 1978, FEBS letters.

[27]  R. Palmiter,et al.  Correlation of procollagen mRNA levels in normal and transformed chick embryo fibroblasts with different rates of procollagen synthesis. , 1978, Biochemistry.

[28]  G. Carmichael,et al.  Analysis of single- and double-stranded nucleic acids on polyacrylamide and agarose gels by using glyoxal and acridine orange. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[29]  P Berg,et al.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. , 1977, Journal of molecular biology.

[30]  Dash Rj,et al.  Insulin and proinsulin content of pancreases from diabetic and nondiabetic subjects. , 1973 .

[31]  R. Dash,et al.  Insulin and Proinsulin Content of Pancreases from Diabetic and Nondiabetic Subjects , 1973, Diabetes.

[32]  M. Permutt,et al.  Insulin biosynthesis. I. On the mechanism of glucose stimulation. , 1972, The Journal of biological chemistry.

[33]  G. Morris,et al.  The effect of glucose on insulin biosynthesis by isolated islets of Langerhans of the rat. , 1970, Biochimica et biophysica acta.

[34]  P. Lacy,et al.  The Effect of Hyperglycemia upon Islet Regeneration in Rats , 1963, Diabetes.

[35]  P. Lacy,et al.  The Prediabetic Period in Partially Pancreatectomized Rats , 1963, Diabetes.

[36]  R. Ogilvie,et al.  Quantitative Estimation of the Pancreatic Islet Tissue in Diabetic Subjects , 1955, Diabetes.

[37]  G. Wrenshall,et al.  Extractable Insulin of Pancreas: Correlation with Pathological and Clinical Findings in Diabetic and Nondiabetic Cases , 1952, Diabetes.

[38]  F. Dohan,et al.  Lesions of the Pancreatic Islets Produced in Cats by Administration of Glucose , 1947, Science.

[39]  A. Marble,et al.  ISLAND HYPERPLASIA IN THE PARTIALLY DEPANCREATIZED RAT , 1941 .