Fetal tissue transplantation has gathered considerable interest among
researchers dealing with organ transplantation. A large number of stud
ies concerning fetal intestinal transplantation have been published in
the past 2 decades, almost all of them aiming to determine the feasib
ility of a properly functioning fetal transplant in continuity with th
e host's own enteral system. This study was designed to determine the
absorptive capacity of the neogut in vivo, without anastomosing the tr
ansplant to the host's intestine, and to evaluate its use as an access
ory enteral segment. Intestinal segments taken from Wistar albino fetu
ses were transplanted subcutaneously into the abdominal wall of 20 Spr
ague-Dawley rats. Immunosuppression was maintained by daily cyclospori
n A (Cy A) 10 mg/kg injections s.c. and evaluated by determination of
serum Cy A level and T-helper/T-suppressor cell ratio. The neogut was
converted into a Thiry-Vella loop 2 weeks after transplantation. A tes
t solution composed of 20% glucose and Trophamine was perfused via the
stomas; glucose and amino acid absorption gradients were calculated.
The gamma-glutamyl transferase (GGT) activity and mitotic index of the
neogut were determined. Results were compared to those obtained from
the host. There was no significant difference (P > 0.05) in glucose ab
sorption between the neogut and the host tissue. Amino acid absorption
and specific GGT activity were significantly less (P < 0.01) in the n
eogut. There was no significant difference (P > 0.05) between neogut a
nd host intestine in mitotic index. Our data support the idea of using
a transplanted fetal intestinal segment as an accessory feeding route
.