In isoprenaline-treated rats, BPC‑157 given 5 min after isoprenaline attenuated the early multiorgan failure, thrombosis, venous hypertension and aortal hypotension via azygos vein activation.
In plain wordsIn rats given isoprenaline, BPC‑157 lessened early organ damage, clots and blood pressure changes.
- Peptide
- BPC-157
- Outcome
- DecreaseEarly multiorgan failure, thrombosis and pressure disturbances after isoprenaline
- Study
ratn: not reported in source
Isoprenaline-induced myocardial infarction and reinfarction- Outcome group
- Cardiovascular events · Cardiovascular
- Studied dose
- 10 ng/kg and 10 µg/kg · intraperitonealAs given in this study (rat).
Source sentences
At 30 min after isoprenaline 75 mg/kg s.c., we noted an early multiorgan failure (brain, heart, lung, liver, kidney and gastrointestinal lesions), thrombosis, intracranial (superior sagittal sinus) hypertension, portal and caval hypertension, and aortal hypotension, in its full presentation (or attenuated by BPC 157 therapy (given at 5 min after isoprenaline) via activation of the azygos vein)
3 context sentences(design, population, supporting numbers)
Stable Gastric Pentadecapeptide BPC 157 May Counteract Myocardial Infarction Induced by Isoprenaline in Rats.
BPC 157 (10 ng/kg, 10 µg/kg i.p.), L-NAME (5 mg/kg i.p.), and L-arginine (200 mg/kg i.p.) were given alone or together at (i) 30 min before or, alternatively, (ii) at 5 min after isoprenaline (75 or 150 mg/kg s.c.).
Further, we studied isoprenaline (75 or 150 mg/kg s.c.) myocardial infarction (1 challenge) and reinfarction (isoprenaline at 0 h and 24 h, 2 challenges) in rats (assessed at the end of the subsequent 24 h period).