RAT ISLET ISOGRAFT FUNCTION - EFFECT OF GRAFT VOLUME AND TRANSPLANTATION SITE

被引:37
作者
VANSUYLICHEM, PTR [1 ]
STRUBBE, JH [1 ]
HOUWING, H [1 ]
WOLTERS, GHJ [1 ]
VANSCHILFGAARDE, R [1 ]
机构
[1] UNIV GRONINGEN,DEPT ANIM PHYSIOL,9750 AA HAREN,NETHERLANDS
关键词
D O I
10.1097/00007890-199404150-00005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Islet isograft function was analyzed after transplantation of 4 well-defined endocrine volumes (12.5%, 25%, 50%, and 100% of the endocrine volume in the normal adult rat pancreas) to 3 different sites (kidney, liver, and spleen). Graft function was tested in unanesthetized, unstressed rats by the responses to glucose infusion and to a meal, All animals with grafts greater than or equal to 25% of the endocrine volume of the rat pancreas returned to normoglycemia after transplantation. The minimal graft volume for restoring normoglycemia is probably between 12.5% and 25%, since also a small number of grafts of 12.5% were successful. At 1 month, basal glucose and insulin levels were similar to those of controls in rats with grafts to the spleen, but higher in rats with grafts to the kidney or liver. Irrespective of the transplantation site, recipients had higher glucose and lower insulin levels than controls in response to glucose infusion. In response to a meal, however, only the first-phase insulin response was reduced, but the total insulin output during the entire test was similar to that of controls. Graft performance was found to be graft-size dependent. Results of tests performed at 2 months showed a tendency of increasing responsiveness compared with the results of tests at 1 month.
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页码:1010 / 1017
页数:8
相关论文
共 35 条
[1]   NATURAL-HISTORY OF INTRAHEPATIC CANINE ISLET CELL AUTOGRAFTS [J].
ALEJANDRO, R ;
CUTFIELD, RG ;
SHIENVOLD, FL ;
POLONSKY, KS ;
NOEL, J ;
OLSON, L ;
DILLBERGER, J ;
MILLER, J ;
MINTZ, DH .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 78 (05) :1339-1348
[2]  
ARRAJAB A, 1989, ACTA CHIR SCAND, V155, P503
[3]   PARTIAL PANCREATECTOMY IN THE RAT AND SUBSEQUENT DEFECT IN GLUCOSE-INDUCED INSULIN RELEASE [J].
BONNERWEIR, S ;
TRENT, DF ;
WEIR, GC .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 71 (06) :1544-1553
[4]   PHYSIOLOGICAL IMPORTANCE OF DEFICIENCY IN EARLY PRANDIAL INSULIN-SECRETION IN NON-INSULIN-DEPENDENT DIABETES [J].
BRUCE, DG ;
CHISHOLM, DJ ;
STORLIEN, LH ;
KRAEGEN, EW .
DIABETES, 1988, 37 (06) :736-744
[5]  
CHILD CG, 1969, SURG GYNECOL OBSTET, V124, P49
[6]   NEW DEVELOPMENTS IN THE INCRETIN CONCEPT [J].
CREUTZFELDT, W ;
EBERT, R .
DIABETOLOGIA, 1985, 28 (08) :565-573
[7]  
FELDMAN SD, 1977, SURGERY, V82, P386
[8]   QUANTITATIVE-ANALYSIS OF PANCREATIC-ISLET DEVELOPMENT AND INSULIN STORAGE IN FETAL AND NEWBORN RAT [J].
FREIE, HMP ;
PASMA, A ;
BOUMAN, PR .
ACTA ENDOCRINOLOGICA, 1975, 80 (04) :657-666
[9]   EFFECT OF ALGINATE-POLYLYSINE-ALGINATE MICROENCAPSULATION ON INVITRO INSULIN RELEASE FROM RAT PANCREATIC-ISLETS [J].
FRITSCHY, WM ;
WOLTERS, GHJ ;
VANSCHILFGAARDE, R .
DIABETES, 1991, 40 (01) :37-43
[10]   INSULIN AND GLUCAGON-SECRETION AFTER PANCREATECTOMIES - CORRELATION OF SECRETION AND HORMONAL CONTENTS OF REMAINING PANCREAS [J].
GOTOH, M ;
MONDEN, M ;
OKAMURA, J ;
MORI, T ;
SHIMA, K .
DIABETES, 1989, 38 (07) :861-867