199 results match your criteria: "Surgical-Medical Research Institute[Affiliation]"
Transplantation
October 1997
Surgical-Medical Research Institute and Department of Surgery, University of Alberta, Edmonton, Canada.
Background: Inasmuch as cryopreservation can facilitate clinical islet transplantation by providing a means of storing supplemental islets in order to augment marginally adequate grafts, protocols are needed to allow for a minimal loss in viable beta cells. By replacing the cryoprotectant dimethyl sulfoxide (DMSO) with ethylene glycol (EG), a more simplified cryopreservation protocol was developed, which resulted in improved survival and function of rat pancreatic islets.
Methods: Nonfrozen islets, islets cryopreserved in DMSO, and EG-cryopreserved islets were compared for percent recovery, cellular composition, in vitro viability, and metabolic function after transplantation.
Transplant Proc
June 1997
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Transplant Proc
June 1997
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Transplant Proc
June 1997
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Transplant Proc
June 1997
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Diabetes
February 1997
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
We prepared single-cell suspensions of Lewis rat ¿RT1(1/l)¿ testicular cells and cultured these in vitro for 48 h under conditions that promoted the formation of cellular aggregates. In the absence of systemic immunosuppression, the transplantation of a sufficient quantity of these aggregates (containing 11 x 10(6) cells, (75% Sertoli cells), together with 2,000 purified Lewis rat islets, reversed the diabetic state for >95 days in 100% (5/5) of the chemically diabetic Wistar-Furth ¿RT1(u/u)¿ recipients. Similar grafts consisting of islets alone or islets plus 50% fewer testicular cell aggregates survived for only 10 days.
View Article and Find Full Text PDFAdv Exp Med Biol
May 1998
Department of Surgery, Surgical-Medical Research Institute, University of Alberta, Edmonton.
Transplantation
August 1996
Surgical Medical Research Institute, University of Alberta, Edmonton, Canada.
This study examined the effects of dibutyryl-cyclic adenosine monophosphate (db-cAMP) and okadaic acid (a specific inhibitor of protein phosphatases 1 and 2A) as additives to a cold storage solution. The effects on levels of glycogen phosphorylase, the resultant effects on flux through the glycolytic pathway, and the consequences of these changes on adenylate (ATP, ADP, and AMP) levels in rat liver during a 24-hr period of cold hypoxia were studied. The rapid transition to anaerobic metabolism was reflected in the increases in lactate levels for all groups.
View Article and Find Full Text PDFJ Biol Chem
June 1996
Lipid and Lipoprotein Research Group, Surgical-Medical Research Institute, University of Alberta, Edmonton, Alberta T6G 2S2, Canada.
We have investigated the cell death of a Chinese hamster ovary mutant (MT-58) with a thermo-sensitive CTP:phosphocholine cytidylyltransferase, the rate-limiting enzyme of the CDP-choline pathway for phosphatidylcholine biosynthesis (Esko, J. D., Wermuth, M.
View Article and Find Full Text PDFTransplantation
June 1996
Surgical-Medical Research Institute, University of Alberta, Canada.
To utilize gene therapy, we required an efficient method to transfect intact islets before their use in transplantation. The biolistic method transforms cells by bombarding them with microprojectiles coated with DNA. Once internalized, the DNA is solubilized and expressed.
View Article and Find Full Text PDFJ Clin Invest
May 1996
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Based upon existing methods of isolating fetal porcine islet tissue, a simple, reliable procedure was developed for the preparation of porcine neonatal islet cell aggregates with a reproducible and defined cellular composition. After 9 d of in vitro culture, tissue from one neonatal pig pancreas yielded approximately 50,000 islet cell aggregates, consisting of primarily epithelial cells (57%) and pancreatic endocrine cells (35%). During the culture period, the total beta cell mass decreased initially, but subsequently increased 1.
View Article and Find Full Text PDFTransplantation
April 1996
Department of Surgery, and the Surgical-Medical Research Institute, University of Alberta, Canada.
In an attempt to reduce the variability in the yields of human islets isolations and to identify donor factors that were potentially deleterious, we retrospectively reviewed 153 human islets isolations in our center over a 3-year period. Isolations were performed using controlled collagenase perfusion via the duct, automated dissociation, and Ficoll purification. Factors leading to successful isolations (recovery of >100,000 islet equivalents at a purity >50%) were analyzed retrospectively using univariate and multivariate analysis.
View Article and Find Full Text PDFTransplant Proc
April 1996
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Cryobiology
February 1996
Surgical Medical Research Institute, University of Alberta, Edmonton, Alberta, T6G 2N8, Canada.
The current study was undertaken to investigate energy metabolism during hypoxia in the cold in livers from euthermic and hibernating Columbian ground squirrels. We hypothesized that the hibernating Columbian ground squirrel would be able to maintain liver energetics for a considerably longer time than euthermic animals. Particular reference was made to the function of glycolysis, which is the only mechanism for energy production under hypothermic ischemia.
View Article and Find Full Text PDFTransplant Proc
February 1996
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Transplant Proc
December 1995
Surgical-Medical Research Institute, University of Alberta, Edmonton.
Transplant Proc
December 1995
Surgical-Medical Research Institute, University of Alberta, Edmonton.
Transplant Proc
December 1995
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Transplant Proc
December 1995
Surgical Medical Research Institute, University of Alberta, Edmonton.
Transplant Proc
December 1995
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Transplant Proc
December 1995
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Transplant Proc
December 1995
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Transplant Proc
December 1995
Surgical-Medical Research Institute, University of Alberta, Edmonton, Canada.
Transplant Proc
December 1995
Surgical-Medical Research Institute, Edmonton, Alberta, Canada.
Transplant Proc
December 1995
Surgical-Medical Research Institute, Edmonton, Alberta, Canada.