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SHR Neuro Cancer Cardio Lipid Metab Microb

Skorjanec, S; Dolovski, Z; Kocman, I; Brcic, L; Blagaic Boban, A; Batelja, L; Coric, M; Sever, M; Klicek, R; Berkopic, L; Radic, B; Drmic, D; Kolenc, D; Ilic, S; Cesarec, V; Tonkic, A; Zoricic, I; Mise, S; Staresinic, M; Ivica, M; Lovric Bencic, M; Anic, T; Seiwerth, S; Sikiric, P.
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.
Dig Dis Sci. 2009; 54(1): 46-56. Doi: 10.1007/s10620-008-0332-9
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Abstract:
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 microg/kg) (12 ml/rat/day) or intraperitoneally (10 microg/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.
Find related publications in this database (using NLM MeSH Indexing)
Adrenal Cortex Hormones - pharmacology Adrenal Cortex Hormones - therapeutic use
Animals -
Anti-Ulcer Agents - pharmacology Anti-Ulcer Agents - therapeutic use
Atropine - pharmacology Atropine - therapeutic use
Cutaneous Fistula - drug therapy Cutaneous Fistula - pathology
Disease Models, Animal -
Gastric Fistula - drug therapy Gastric Fistula - pathology
Gastric Mucosa - drug effects
Male -
Omeprazole - pharmacology Omeprazole - therapeutic use
Peptide Fragments - pharmacology Peptide Fragments - therapeutic use
Proteins - pharmacology Proteins - therapeutic use
Ranitidine - pharmacology Ranitidine - therapeutic use
Rats -
Rats, Wistar -
Stomach Ulcer - drug therapy Stomach Ulcer - pathology
Wound Healing - drug effects

Find related publications in this database (Keywords)
Unhealed gastrocutaneous fistulas
Stable gastric pentadecapeptide BPC 157
Atropine
Ranitidine
Omeprazole
Analogous healing
Persistent skin ulcer
Persistent gastric ulcer
Rat
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