Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

Stable gastric pentadecapeptide BPC 157 therapy for monocrotaline-induced pulmonary hypertension in rats leads to prevention and reversal (CROSBI ID 297111)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Udovičić, Mario ; Sever, Marko ; Kavur, Lovro ; Lončarić, Kristina ; Barišić, Ivan ; Balenović, Diana ; Živanović Posilović, Gordana ; Strinić, Dean ; Uzun, Sandra ; Batelja Vuletić, Lovorka et al. Stable gastric pentadecapeptide BPC 157 therapy for monocrotaline-induced pulmonary hypertension in rats leads to prevention and reversal // Biomedicines, 9 (2021), 7; 822, 17. doi: 10.3390/biomedicines9070822

Podaci o odgovornosti

Udovičić, Mario ; Sever, Marko ; Kavur, Lovro ; Lončarić, Kristina ; Barišić, Ivan ; Balenović, Diana ; Živanović Posilović, Gordana ; Strinić, Dean ; Uzun, Sandra ; Batelja Vuletić, Lovorka ; Sikirić, Sunčana ; Škrtić, Anita ; Drmić, Domagoj ; Boban Blagaić, Alenka ; Lovrić Benčić, Martina ; Seiwerth, Sven ; Sikirić, Predrag

engleski

Stable gastric pentadecapeptide BPC 157 therapy for monocrotaline-induced pulmonary hypertension in rats leads to prevention and reversal

Monocrotaline selectively injures the lung’s vascular endothelium and induces pulmonary arterial hypertension. The stable gastric pentadecapeptide BPC 157 acts as a prototype cytoprotective agent that maintains endothelium, and its application may be a novel therapy. Besides, BPC 157 prevents and reverses thrombosis formation, maintains platelet function, alleviates peripheral vascular occlusion disturbances, and has anti-arrhythmic and anti-inflammatory effects. Monocrotaline-induced pulmonary arterial hypertension in rats (wall thickness, total vessel area, heart frequency, QRS axis deviation, QT interval prolongation, increase in right ventricle systolic pressure and bodyweight loss) can be counteracted with early or delayed BPC 157 therapy. Methods and Results. After monocrotaline (80 mg/kg subcutaneously), BPC 157 (10 g/kg or 10 ng/kg, days 1–14 or days 1–30 (early regimens), or days 14–30 (delayed regimen)) was given once daily intraperitoneally (last application 24 h before sacrifice) or continuously in drinking water until sacrifice (day 14 or 30). Without therapy, the outcome was the full monocrotaline syndrome, marked by right-side heart hypertrophy and massive thickening of the precapillary artery’s smooth muscle layer, clinical deterioration, and sometimes death due to pulmonary hypertension and right-heart failure during the 4th week after monocrotaline injection. With all BPC 157 regimens, monocrotaline-induced pulmonary arterial hypertension (including all disturbed parameters) was counteracted, and consistent beneficial effects were documented during the whole course of the disease. Pulmonary hypertension was not even developed (early regimens) as quickly as the advanced pulmonary hypertension was rapidly attenuated and then completely eliminated (delayed regimen). Conclusions. Thus, pentadecapeptide BPC 157 prevents and counteracts monocrotaline-induced pulmonary arterial hypertension and cor pulmonale in rats.

monocrotaline ; pentadecapeptide BPC 157 ; rat ; pulmonary arterial hypertension

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

9 (7)

2021.

822

17

objavljeno

2227-9059

10.3390/biomedicines9070822

Povezanost rada

Temeljne medicinske znanosti

Poveznice
Indeksiranost