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Therapy for Unhealed Gastrocutaneous Fistulas in Rats as a Model for Analogous Healing of Persistent Skin Wounds and Persistent Gastric Ulcers: Stable Gastric Pentadecapeptide BPC 157, Atropine, Ranitidine, and Omeprazole (CROSBI ID 147651)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Škorjanec, Sandra ; Dolovski, Zdravko ; Kocman, Ivan ; Brčić, Luka ; Boban Blagaić, Alenka ; Batelja, Lovorka ; Ćorić, Marijana ; Sever, Marko ; Kliček, Robert ; Berkopić, Lidija et al. Therapy for Unhealed Gastrocutaneous Fistulas in Rats as a Model for Analogous Healing of Persistent Skin Wounds and Persistent Gastric Ulcers: Stable Gastric Pentadecapeptide BPC 157, Atropine, Ranitidine, and Omeprazole // Digestive diseases and sciences, 54 (2009), 1; 46-56. doi: 10.1007/s10620-008-0332-9

Podaci o odgovornosti

Škorjanec, Sandra ; Dolovski, Zdravko ; Kocman, Ivan ; Brčić, Luka ; Boban Blagaić, Alenka ; Batelja, Lovorka ; Ćorić, Marijana ; Sever, Marko ; Kliček, Robert ; Berkopić, Lidija ; Radić, Božo ; Drmić, Domagoj ; Kolenc, Danijela ; Ilić, Spomenko ; Cesarec, Vedran ; Tonkić, Ante ; Zoričić, Ivan ; Miše, Stjepan ; Starešinić, Mario ; Ivica, Mihovil ; Lovrić Benčić, Martina ; Anić, Tomislav ; Seiwerth, Sven ; Sikirić, Predrag

engleski

Therapy for Unhealed Gastrocutaneous Fistulas in Rats as a Model for Analogous Healing of Persistent Skin Wounds and Persistent Gastric Ulcers: Stable Gastric Pentadecapeptide BPC 157, Atropine, Ranitidine, and Omeprazole

This study focused on unhealed gastrocutaneous fistulas to resolve whether standard drugs that promote healing of gastric ulcers may simultaneously have the same effect on cutaneous wounds, and corticosteroid aggravation, and to demonstrate why peptides such as BPC 157 exhibit a greater healing effect. Therefore, with the fistulas therapy, we challenge the wound/growth factors theory of the analogous nonhealing of wounds and persistent gastric ulcers. The healing rate of gastrocutaneous fistula in rat (2-mm-diameter stomach defect, 3-mm-diameter skin defect) validates macro/microscopically and biomechanically a direct skin wound/stomach ulcer relation, and identifies a potential therapy consisting of: (i) stable gastric pentadecapeptide BPC 157 [in drinking water (10 mu g/kg) (12 ml/rat/day) or intraperitoneally (10 mu g/kg, 10 ng/kg, 10 pg/kg)], (ii) atropine (10 mg/kg), ranitidine (50 mg/kg), and omeprazole (50 mg/kg), (iii) 6-alpha-methylprednisolone (1 mg/kg) [intraperitoneally, once daily, first application at 30 min following surgery ; last 24 h before sacrifice (at postoperative days 1, 2, 3, 7, 14, and 21)]. Greater anti-ulcer potential and efficiency in wound healing compared with standard agents favor BPC 157, efficient in inflammatory bowel disease (PL-14736, Pliva), given in drinking water or intraperitoneally. Even after 6-alpha-methylprednisolone aggravation, BPC 157 promptly improves both skin and stomach mucosa healing, and closure of fistulas, with no leakage after up to 20 ml water intragastrically. Standard anti-ulcer agents, after a delay, improve firstly skin healing and then stomach mucosal healing, but not fistula leaking and bursting strength (except for atropine). We conclude that BPC 157 may resolve analogous nonhealing of wounds and persistent gastric ulcers better than standard agents.

unhealed gastrocutaneous fistulas ; stable gastric pentadecapeptide bpc 157 ; atropine ; ranitidine ; omeprazole ; analogous healing ; persistent skin ulcer ; persistent gastric ulcer ; rat

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Podaci o izdanju

54 (1)

2009.

46-56

objavljeno

0163-2116

10.1007/s10620-008-0332-9

Povezanost rada

Temeljne medicinske znanosti

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