TY - JOUR
T1 - Distribution of blood flow to the gastroutestinal tract of swine during t-2 toxin-induced shock
AU - Beasley, Val Richard
AU - Lundeen, Gregg R.
AU - Poppenga, Robert H.
AU - Buck, William B.
N1 - Funding Information:
This project was supported in part by U.S. Army Medical Research and Development Command, Contract DAMD 82-C-2179. The opinions and/or findings contained in this report are those of the authors and should not be construed as an official Department of the Army position, policy, or decision unless so designated by other documentation. The authors thank Steven P. Swanson and Harold Dean Rood, Jr., for providing the purified toxin, and Richard Manuel and Jackie Renee Mariner for their excellent technical assistance.
PY - 1987/10
Y1 - 1987/10
N2 - Swine (6 per group) were used to study gastrointestinal blood flow during T-2 toxin-induced shock. Low- and high-dose groups were given T-2 toxin at 0.6 or 2.4 mg/kg via the pulmonary artery; controls were given the ethanol vehicle. Radiolabeled microspheres were administered into the left atrium to assess organ blood flow predosing and at 90-mm intervals for 6 hr. Gastric blood flow decreased in both T-2 groups, and at 6 hr the highdose group's value was 17% of the predose value. In the low-dose group, the lowest gastric blood flow (30% of predose) was observed 3 hr postdosing. Small-intestinal blood flow of the control group declined to 64% of the predose value. In the high-dose group, small-intestinal blood flow at 3 hr was 174% of predose, followed by a reduction to 62% at 6 hr, coinciding with a severe decline in cardiac output. Small-intestinal blood flow of the low-dose group was 159% of predose at 1.5 hr, then declined to the control value. The high-dose group's large-intestinal blood flow increased to 177% of predose at 3 hr, then declined to 66% at 6 hr. The low-dose group's large-intestinal blood flow increased to 200% of the predose value. The severe decline in gastric blood flow is probably related to the development in swine (given high doses of T-2 toxin) of a g"rossly bright red gastric fundus, with histologic evidence of vascular congestion and mucosal deteriora tion. The initial increase in blood flow to the intestine may contribute to its tolerance to sublethal doses of T-2 toxin and may facilitate the rapid intestinal absorption of the toxin.
AB - Swine (6 per group) were used to study gastrointestinal blood flow during T-2 toxin-induced shock. Low- and high-dose groups were given T-2 toxin at 0.6 or 2.4 mg/kg via the pulmonary artery; controls were given the ethanol vehicle. Radiolabeled microspheres were administered into the left atrium to assess organ blood flow predosing and at 90-mm intervals for 6 hr. Gastric blood flow decreased in both T-2 groups, and at 6 hr the highdose group's value was 17% of the predose value. In the low-dose group, the lowest gastric blood flow (30% of predose) was observed 3 hr postdosing. Small-intestinal blood flow of the control group declined to 64% of the predose value. In the high-dose group, small-intestinal blood flow at 3 hr was 174% of predose, followed by a reduction to 62% at 6 hr, coinciding with a severe decline in cardiac output. Small-intestinal blood flow of the low-dose group was 159% of predose at 1.5 hr, then declined to the control value. The high-dose group's large-intestinal blood flow increased to 177% of predose at 3 hr, then declined to 66% at 6 hr. The low-dose group's large-intestinal blood flow increased to 200% of the predose value. The severe decline in gastric blood flow is probably related to the development in swine (given high doses of T-2 toxin) of a g"rossly bright red gastric fundus, with histologic evidence of vascular congestion and mucosal deteriora tion. The initial increase in blood flow to the intestine may contribute to its tolerance to sublethal doses of T-2 toxin and may facilitate the rapid intestinal absorption of the toxin.
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U2 - 10.1093/toxsci/9.3.588
DO - 10.1093/toxsci/9.3.588
M3 - Article
C2 - 3692016
AN - SCOPUS:77957179082
SN - 1096-6080
VL - 9
SP - 588
EP - 594
JO - Toxicological Sciences
JF - Toxicological Sciences
IS - 3
ER -