## Abstract Thirty‐six male Lewis rats rendered diabetic using alloxan received syngeneic pancreaticoduodenal grafts. Seven days prior to and 7, 30, and 90 days posttransplantation, the animals were housed in metabolic cages for periods of 48 hours. During this time, body weight, water intake, food
Metabolic effect of pancreaticoduodenal transplantation in diabetic rats
✍ Scribed by César T. Spadella; Luiz C. Breim; Maria C. S. Mercadante; Célia S. De Macedo; Arthur R. De Macedo
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 543 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0738-1085
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Outbred Wistar rats were randomly assigned to three experimental groups: GI, 10 nondiabetic control rats; GII, 10 alloxan‐diabetic control rats; GIII, 25 alloxan‐diabetic rats that received pancreaticoduodenal transplantation (PDT) from normal donor Wistar rats and were immunosuppressed with cyclosporin A. For 7 prior and 4, 7, 14, 21, and 30 days posttransplantation (during which the animals were housed in metabolic cages for periods of 24 hours) body weight, water and food intake, urine output, blood and urinary glucose, plasma insulin, and glucagon were recorded. These parameters were also concurrently recorded for diabetic and nondiabetic control rats. Animals were sacrificed after 30 days and histological and immunohistochemical studies of the pancreas were performed. Pancreatic transplants consistently and significantly improved the metabolic abnormalities of the diabetic rat (P<0.01) by restoring body weight gain, and by immediate relief of hyperglycemia, glucosuria, polyuria, polydipsia, and also the low levels of plasma insulin. The plasma glucagon, elevated in diabetic control rats, did not change after transplant. © 1992 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract The objective of this work was to establish a stable and simple simultaneous pancreaticoduodenal‐kidney transplantation model in rats. The methods involved harvesting a pancreaticoduodenal‐kidney (left) (PDK) and 1‐cm inferior vena cava (IVC) with a 0.5‐cm left and right iliac communis
Previous studies have demonstrated a major difference in mevalonate metabolism by male and female rats by both the shunt and sterol pathways. This important sex difference was shown to be related to the presence of oestrogens and/or progesterone. In the present study we have investigated the effects