Mj. Myers et al., EFFECT OF GROWTH-HORMONE OR CHROMIUM PICOLINATE ON SWINE METABOLISM AND INFLAMMATORY CYTOKINE PRODUCTION AFTER ENDOTOXIN CHALLENGE EXPOSURE, American journal of veterinary research, 58(6), 1997, pp. 594-600
Objective-To determine whether recombinant porcine somatotropin (PST)
or chromium picolinate (CrP) affected cytokine production and metaboli
sm in swine after endotoxin challenge exposure. Animals-20 Poland Chin
a x Landrace pigs, 5/group. Procedure-Pigs were given CrP-supplemented
feed at body weight of 20 kg; PST treatment began at 60 kg, and both
treatments continued through body weight of 90 kg, At 90 kg, pigs were
challenge exposed with 20 mu g of lipopolysaccharide (LPS)/kg of body
weight. Blood samples were obtained at various times through 24 hours
after LPS challenge exposure. Results-in all pigs not given PST, gluc
ose concentration decreased 2 to 4 hours after LPS. In PST-treated pig
s, blood glucose concentration was decreased at 6 to 8 hours after LPS
. Plasma insulin concentration paralleled changes in glucose concentra
tion. Nonesterified fatty acid concentration was high 2 to 24 hours af
ter IFS in pigs not given PST and at 6 to 24 h in PST-treated pigs. Pl
asma urea nitrogen concentration was high at 6 to 24 hours after LPS i
n pigs not given PST. The urea nitrogen values in PST-treated pigs wer
e lower at ail times. Serum aspartate transaminase activity was high 6
to 24 hours after LPS in pigs not given PST, whereas PST treatment pr
evented the increase in this enzyme activity. In untreated (PST) pigs,
plasma bilirubin (total and direct) concentrations were high 4 to 8 h
ours after LPS and returned to normal at 24 hours. The PST- and CrP-tr
eated pigs maintained normal plasma bilirubin concentrations. interleu
kin 6 activity was unaffected by CrP and PST treatments. Treatment wit
h CrP and PST decreased the tumor necrosis factor alpha response to IF
S, compared with that in control pigs. Conclusions-PST, and to a lesse
r extent CrP, provide protection against the adverse metabolic effects
of LPS-induced septic shock.