TY - JOUR
T1 - Glutamine protects function and improves preservation of small bowel segments
AU - Sasaki, Kazuaki
AU - Park, James O.
AU - Bain, Allison
AU - Reilly, Kathleen J.
AU - Adamson, William T.
AU - Koide, Shinji
AU - Zhang, Wei
AU - Rombeau, John L.
PY - 1997/11
Y1 - 1997/11
N2 - Background: Improved organ preservation is essential for the success of small bowel transplantation. Small bowel is usually preserved in UW (University of Wisconsin) solution which does not contain glutamine (Gln), the principal fuel for the enterocyte. We hypothesized that Gin-supplemented UW would improve mucosal function and structure of cold preserved small intestine. Materials and methods: Jejunum (40 cm) was harvested from Lewis rats and preserved for 18 hr at 4°C in saline; UW solution only; UW with 1, 2, or 4% Gln; and UW containing 1, 2, or 4% isonitrogenous balanced nonessential amino acids (NEAA). 14C glucose transport, mucosal protein, mucosal maltase and alkaline phosphatase, jejunal villous height, and histologic damage were measured. Results: UW with 2% Gln significantly increased glucose transport and mucosal protein when compared to the 2% NEAA and UW-only groups. Two percent Gln significantly decreased histologic damage of jejunum following cold preservation. Increasing Gin to 4% did not significantly increase its efficacy when compared to the UW with 2% Gln group. There were no significant differences in the activities of mucosal maltase and alkaline phosphatase among the various treatment groups. Conclusions: The addition of Gln, optimally provided at a concentration of 2%, to UW solution may protect the preserved small bowel segments from cold ischemic injury and improve mucosal function.
AB - Background: Improved organ preservation is essential for the success of small bowel transplantation. Small bowel is usually preserved in UW (University of Wisconsin) solution which does not contain glutamine (Gln), the principal fuel for the enterocyte. We hypothesized that Gin-supplemented UW would improve mucosal function and structure of cold preserved small intestine. Materials and methods: Jejunum (40 cm) was harvested from Lewis rats and preserved for 18 hr at 4°C in saline; UW solution only; UW with 1, 2, or 4% Gln; and UW containing 1, 2, or 4% isonitrogenous balanced nonessential amino acids (NEAA). 14C glucose transport, mucosal protein, mucosal maltase and alkaline phosphatase, jejunal villous height, and histologic damage were measured. Results: UW with 2% Gln significantly increased glucose transport and mucosal protein when compared to the 2% NEAA and UW-only groups. Two percent Gln significantly decreased histologic damage of jejunum following cold preservation. Increasing Gin to 4% did not significantly increase its efficacy when compared to the UW with 2% Gln group. There were no significant differences in the activities of mucosal maltase and alkaline phosphatase among the various treatment groups. Conclusions: The addition of Gln, optimally provided at a concentration of 2%, to UW solution may protect the preserved small bowel segments from cold ischemic injury and improve mucosal function.
KW - Cold preservation
KW - Glutamine
KW - Small bowel transplantation
KW - Transplantation/immunology
UR - https://www.scopus.com/pages/publications/0031278064
U2 - 10.1006/jsre.1997.5186
DO - 10.1006/jsre.1997.5186
M3 - Article
C2 - 9441799
AN - SCOPUS:0031278064
SN - 0022-4804
VL - 73
SP - 90
EP - 94
JO - Journal of Surgical Research
JF - Journal of Surgical Research
IS - 1
ER -