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Bypassing major venous occlusion and duodenal lesions in rats, and therapy with the stable gastric pentadecapeptide BPC 157, L-NAME and L-arginine.
Amic, Fedor; Drmic, Domagoj; Bilic, Zdenko; Krezic, Ivan; Zizek, Helena; Peklic, Marina; Klicek, Robert; Pajtak, Alen; Amic, Enio; Vidovic, Tinka; Rakic, Mislav; Milkovic Perisa, Marija; Horvat Pavlov, Katarina; Kokot, Antonio; Tvrdeic, Ante; Boban Blagaic, Alenka; Zovak, Mario; Seiwerth, Sven; Sikiric, Predrag.
Afiliação
  • Amic F; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Drmic D; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Bilic Z; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Krezic I; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Zizek H; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Peklic M; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Klicek R; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Pajtak A; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Amic E; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Vidovic T; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Rakic M; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Milkovic Perisa M; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Horvat Pavlov K; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Kokot A; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Tvrdeic A; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Boban Blagaic A; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Zovak M; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Seiwerth S; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
  • Sikiric P; Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb 10000, Croatia.
World J Gastroenterol ; 24(47): 5366-5378, 2018 Dec 21.
Article em En | MEDLINE | ID: mdl-30598581
ABSTRACT

AIM:

To investigate whether duodenal lesions induced by major venous occlusions can be attenuated by BPC 157 regardless nitric oxide (NO) system involvement.

METHODS:

Male Wistar rats underwent superior anterior pancreaticoduodenal vein (SAPDV)-ligation and were treated with a bath at the ligated SAPDV site (BPC 157 10 µg, 10 ng/kg per 1 mL bath/rat; L-NAME 5 mg/kg per 1 mL bath/rat; L-arginine 100 mg/kg per 1 mL bath/rat, alone and/or together; or BPC 157 10 µg/kg instilled into the rat stomach, at 1 min ligation-time). We recorded the vessel presentation (filled/appearance or emptied/disappearance) between the 5 arcade vessels arising from the SAPDV on the ventral duodenum side, the inferior anterior pancreaticoduodenal vein (IAPDV) and superior mesenteric vein (SMV) as bypassing vascular pathway to document the duodenal lesions presentation; increased NO- and oxidative stress [malondialdehyde (MDA)]-levels in duodenum.

RESULTS:

Unlike the severe course in the SAPDV-ligated controls, after BPC 157 application, the rats exhibited strong attenuation of the mucosal lesions and serosal congestion, improved vessel presentation, increased interconnections, increased branching by more than 60% from the initial value, the IAPDV and SMV were not congested. Interestingly, after 5 min and 30 min of L-NAME and L-arginine treatment alone, decreased mucosal and serosal duodenal lesions were observed; their effect was worsened at 24 h, and no effect on the collateral vessels and branching was seen. Together, L-NAME+L-arginine antagonized each other's response, and thus, there was an NO-related effect. With BPC 157, all SAPDV-ligated rats receiving L-NAME and/or L-arginine appeared similar to the rats treated with BPC 157 alone. Also, BPC 157 in SAPDV-ligated rats normalized levels of NO and MDA, two oxidative stress markers, in duodenal tissues.

CONCLUSION:

BPC 157, rapidly bypassing occlusion, rescued the original duodenal flow through IAPDV to SMV flow, an effect related to the NO system and reduction of free radical formation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Colite Isquêmica / Circulação Colateral / Substâncias Protetoras / Trombose Venosa / Duodeno Tipo de estudo: Clinical_trials / Etiology_studies Limite: Animals / Humans / Male Idioma: En Revista: World J Gastroenterol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Croácia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Colite Isquêmica / Circulação Colateral / Substâncias Protetoras / Trombose Venosa / Duodeno Tipo de estudo: Clinical_trials / Etiology_studies Limite: Animals / Humans / Male Idioma: En Revista: World J Gastroenterol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Croácia