Z. Grabarevic et al., THE INFLUENCE OF BPC-157 ON NITRIC-OXIDE AGONIST AND ANTAGONIST-INDUCED LESIONS IN BROILER CHICKS, J PHYSL-PAR, 91(3-5), 1997, pp. 139-149
We describe the effects of nitric oxide (NO) agonists and antagonists
and the influence of a novel organoprotective pentadecapeptide BPC 157
, on the development of pulmonary hypertension syndrome and tissue les
ions in chicks. Acute toxicity, which includes single dose application
of saline (1 mt intraperitoneally tip)), BPC 157 (10 mu g/kg bw), L-N
AME (NO antagonist, doses 50, 100, 150 mg/kg bw) and L-arginine (NO ag
onist /100 mg/kg bw with their combination L-NAME + BPC 157; L-NAME L-arginine) was investigated. In this experiment pathohistological exa
mination of the spleen, heart, liver and lungs and hematological analy
sis was conducted. In the chronic toxicity experiment, the animals wer
e treated daily for 5 weeks with L-NAME (10 mg/kg bw), L-arginine (100
mg/kg bw), BPC 157 (10 mu g/kg bw) and their combinations (L-NAME + B
PC 157; L-NAME + L-arginine) ip. Seven animals from each group, includ
ing controls (saline 1 mt ip) were killed every week. Application of L
-NAME caused pulmonary hypertension syndrome (PHS) in the treated chic
ks, which was prevented by the simultaneous application of L-arginine
and BPC 157. Pathohistological examination of both acute and chronic t
oxicity revealed that L-NAME caused severe tissue damage (myocardial a
nd hepatic cell necrosis, necrosis of the lymphoid cells in the spleen
) while L-arginine provoked predominantly congestion, edema and hemorr
hages in all organs. The effect of L-NAME was successfully inhibited b
y the application of L-arginine and BPC 157 but the latter substance d
id not cause any tissue or organ damage. Hematological analysis shows
significant hemoglobin and leukocyte number decrease in the L-NAME-tre
ated groups of chicks.