Rm. Moore et al., SYSTEMIC AND COLONIC VENOUS PLASMA BIOCHEMICAL-ALTERATIONS IN HORSES DURING LOW-FLOW ISCHEMIA AND REPERFUSION OF THE LARGE COLON, Canadian journal of veterinary research, 62(1), 1998, pp. 14-20
The purpose of this study was to determine the effects of low-flow isc
hemia and reperfusion (I-R) of the large colon on 16 systemic venous (
SV) and colonic venous (CV) plasma biochemical variables in horses. Ho
rses (rt = 24) were randomly allocated to 3 groups: sham-operated (n =
6), 6 h ischemia (It = 9), and 3 h ischemia followed by 3 h reperfusi
on (n = 9). SV and CV heparinized blood was collected at 0, 1, 3, 3.25
, 4, and 6 h. The SV-CV difference was calculated for each variable. T
he SV, CV, and SV-CV difference for albumin, total protein, and calciu
m decreased significantly (P < 0.05) across time in horses of all grou
ps, but there were no differences among groups. SV phosphorous was sig
nificantly increased from baseline (BL) at 1 to 6 h in horses of all g
roups, but there were no differences among groups. CV phosphorous was
significantly greater than BL from 1 to 6 h in group-2 horses and from
1 to 3 h in group-3 horses. SV potassium was not different among grou
ps, but was significantly higher at 6 h, compared with BL in horses of
all groups. CV potassium was significantly greater than BL from 1 to
6 h in horses of groups 2 and 3. SV glucose was greater at 6 h compare
d with all previous times in horses of all groups, but there were no d
ifference among groups. CV glucose was significantly lower than BL and
group-1 values in horses of groups 2 and 3 during ischemia, but retur
ned to BL during reperfusion in group-3 horses. CV anion gap was signi
ficantly greater and SV-CV anion gap was significantly more negative i
n horses of groups 2 and 3, compared with group-1 horses during ischem
ia. The biologic relevance of these alterations is unknown, but they m
ay contribute to histopathologic, hemodynamic, and metabolic alteratio
ns characteristic of low-flow I-R. Alternatively, these alterations ma
y simply reflect colonic injury sustained during I-R. Results suggest
that the colon utilizes glucose as a fuel and generates acid anions du
ring low-flow ischemia. Increased CV phosphorous and potassium during
I-R likely occurs as a result of leakage of intracellular stores subse
quent to cellular damage.