C-peptide fragments stimulate glucose utilization in diabetic rats

Studies of C-peptide cellular effects show that not only the full-length native peptide but also specific C-terminal fragments are biologically active in in vitro systems. In the present study, the effect of five C-peptide fragments and the native peptide on whole-body glucose turnover was studied in streptozotocin diabetic rats using the insulin clamp technique. Insulin was infused intravenously at 18 pmol kg^–1 min^–1 for 90 min and blood glucose concentration was clamped at 8 and 4 mM in diabetic and non-diabetic animals. A steady state was reached during the last 30 min of the study period. Rat C-peptide II and fragments comprising residues 27–31 and 28–31 were effective in augmenting glucose turnover in diabetic rats (+100% to 150%), while no significant effects were seen for segments 1–26, 11–19 and 11–15. The metabolic clearance rate for glucose during infusion of C-peptide or fragments 27–31 and 28–31 in diabetic rats was similar to that seen in non-diabetic animals. We conclude that C-terminal tetra- and pentapeptides, but not fragments from the middle segment of C-peptide, are as effective as the full-length peptide in stimulating whole-body glucose turnover in diabetic rats.Received 18 December 2003; received after revision 19 January 2004; accepted 21 January 2004     

Causes of artificially high blood glucose values in experiments with diabetic rats and mice

Summary Unusually high blood sugar values may be caused by the slightest contamination of the blood obtained after puncture of the tail vein by diabetic urine, that has dried onto the tails of the animals. This can be avoided by collecting blood that is allowed to drip from the severed tip of the tail or by carefully cleaning the tail before puncturing the tail vein.     

Causes of artificially high blood glucose values in experiments with diabetic rats and mice

Unusually high blood sugar values may be caused by the slightest contamination of the blood obtained after puncture of the tail vein by diabetic urine, that has dried onto the tails of the animals. This can be avoided by collecting blood that is allowed to drip from the severed tip of the tail or by carefully cleaning the tail before puncturing the tail vein.     

Non-steroidal anti-inflammatory drugs: Effects on the utilization of glucose and production of lactic acid in tissue culture

Zusammenfassung In der Kultur embryonalen Hühnchengewebes kommt es unter Einfluss nichtsteroider Antiphlogistica (Aspirin, Indomethacin, Mefenamicsäure) zu einer Steigerung des Glukoseverbrauchs bei gleichzeitiger Vermehrung der Milchsäureerzeugung. Der Milchsäureverbrauch verläuft in zwei Phasen, wobei der erste Gipfel bei geringsten Konzentrationen des Arzneimittels.auftritt.     

Regulation of glucose transport in Aspergillus nidulans.

Pyruvate and acetate inhibited the uptake of glucose by Aspergillus nidulans; although there were significant variations in glucose uptake rate, the intracellular concentration of acetate was almost identical in biotin-supplemented, normal and deficient cells. The in vitro activity of glucose-binding protein was not affected by biotin, avidin, acetate or acetyl-CoA.     

Leydig cell function in streptozotocin-induced diabetic rats.

Streptozotocin diabetic rats were infertile as a result of decreased Leydig cell function of the testes. The major changes found were: decreased number of Leydig cells and their spontaneous secretion of testosterone. No change in the receptors to LH on the Leydig cells was observed. LH was found to be obligatory for the regulation of Leydig cell function and fertility.     

Alpha-synuclein elicits glucose uptake and utilization in adipocytes through the Gab1/PI3K/Akt transduction pathway

Insulin is the main glucoregulator that promotes the uptake of glucose by tissues and the subsequent utilization of glucose as an energy source. In this paper, we describe a novel glucoregulator, the alpha-synuclein (SNCA) protein, that has previously been linked to Parkinson’s disease. Treatment with recombinant SNCA promotes glucose uptake in vitro in preadipocytes and in vivo in the adipose tissues and skeletal muscles of mice through the LPAR2/Gab1/PI3K/Akt pathway; these effects occur independently of the insulin receptor. This function of SNCA represents a new mechanistic insight that creates novel avenues of research with respect to the process of glucose regulation.     

Forecasting capacity and capacity utilization in the U.S. aerospace industry

The forecasting of capacity and its utilization is particularly relevant in the aerospace industry because of long product delivery lead-times and the forward-pricing system. The objective of this paper is to develop a method for forecasting both the industry's capacity and its capacity utilization so that decision makers who must rely on this information may have policy guidance. The result shows that the aerospace industry's capacity expansion rate is closely tied to its present and recent past state of capacity utilization, and to anticipated changes in output. Output, in turn, can be predicted by using Five Year Defense Plans data and information on the cyclical nature of commercial business. Based on these findings, we were able to build an accurate model for forecasting aerospace industry capacity utilization.     

Shock induces a long-lasting elevation of blood glucose in Aplysia.

Glucose, and not trehalose, was found to be the main blood sugar in Aplysia californica. Changes in blood glucose in response to stress produced by electric shock were measured in blood obtained both from animals dissected within ten minutes of shocking and from catheterized animals at various intervals, up to two and a half hours after the shock. Electric shock increased blood glucose levels. The rise in blood sugar continued as long as two and a half hours after shock.     

Evaluation of monoaminergic receptors in the genetically epilepsy prone rat

The intensity of sound-induced convulsions in the genetically epilepsy-prone rat (GEPR) was reduced in a dose related fashion by intracerebroventricular administration of dobutamine, (beta 1 agonist), terbutaline (beta 2 agonist) or phenylephrine (alpha 1 agonist). BHT-920 (alpha 2 agonist) did not cause a dose-related decrease in sound-induced convulsion intensity. Binding studies showed that whole brain alpha and beta receptor densities (Bmax) were normal while the Kd was increased for the beta ligand in GEPR brain.