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Involvement of MT2 receptors in protective effects of melatonin against cisplatin-induced gastrointestinal damage in mice
Ribeiro, Anita Eugenia Alencar Santos; Ferreira, Eliane Feitosa; Leal, Jaknea dos Santos; Barberino, Ricássio de Sousa; Oliveira, Helinando Pequeno de; Palheta Junior, Raimundo Campos.
  • Ribeiro, Anita Eugenia Alencar Santos; Federal University of São Francisco Valley. Laboratory of Veterinary Pharmacology. Petrolina. BR
  • Ferreira, Eliane Feitosa; Federal University of São Francisco Valley. Laboratory of Veterinary Pharmacology. Petrolina. BR
  • Leal, Jaknea dos Santos; Federal University of São Francisco Valley. Laboratory of Veterinary Pharmacology. Petrolina. BR
  • Barberino, Ricássio de Sousa; Federal University of São Francisco Valley. Nucleus of Biotechnology Applied to Ovarian Follicle Development. Petrolina. BR
  • Oliveira, Helinando Pequeno de; Federal University of São Francisco Valley. Laboratory of Impedance Spectroscopy and Organic Materials. Petrolina. BR
  • Palheta Junior, Raimundo Campos; Federal University of São Francisco Valley. Laboratory of Veterinary Pharmacology. Petrolina. BR
Braz. J. Pharm. Sci. (Online) ; 58: e20476, 2022. graf
Article in English | LILACS | ID: biblio-1403722
ABSTRACT
Abstract Melatonin (MLT) reportedly reduces side effects associated with certain antineoplastic agents. Accordingly, we investigated the effect of MLT on cisplatin (CP)-induced gastric emptying (GE) delay. Mice were intraperitoneally pretreated with vehicle (ethanol 5%; control group), MLT (5, 10, or 20 mg/kg), or N-acetylcysteine (NAC; 150 mg/kg), followed by CP treatment (5 mg/kg). Pharmacological modulation was analyzed using relevant receptor antagonists (luzindole non-selective MT1/MT2 antagonist; 5 mg/kg or 4-P-PDOT selective MT2 antagonist; 4 mg/kg) before treatment with MLT plus CP. All treatments were performed once daily for three days. GE was assessed using phenol red. Gut morphology was examined using scanning electron microscopy and optical microscopy. Compared with the control, CP decreased GE. Pretreatment with NAC and MLT (5 and 10 mg/kg) did not prevent CP-induced gastric dysmotility; however, pretreatment with 20 mg/kg MLT prevented this effect. In addition, luzindole and 4-P-PDOT suppressed MLT-mediated gastroprotection against cytotoxic effects of CP. CP caused degeneration of the gut mucosa, which was attenuated by MLT treatment. Thus, 20 mg/kg MLT prevented the GE delay and decreased CP-induced adverse effects on the gut mucosa. In addition, the gastroprotective activity was mediated via the MT2 receptor.
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Full text: Available Index: LILACS (Americas) Main subject: Receptor, Melatonin, MT2 / Gastrointestinal Diseases / Melatonin Limits: Animals Language: English Journal: Braz. J. Pharm. Sci. (Online) Journal subject: Farmacologia / Terapˆutica / Toxicologia Year: 2022 Type: Article Affiliation country: Brazil Institution/Affiliation country: Federal University of São Francisco Valley/BR

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Full text: Available Index: LILACS (Americas) Main subject: Receptor, Melatonin, MT2 / Gastrointestinal Diseases / Melatonin Limits: Animals Language: English Journal: Braz. J. Pharm. Sci. (Online) Journal subject: Farmacologia / Terapˆutica / Toxicologia Year: 2022 Type: Article Affiliation country: Brazil Institution/Affiliation country: Federal University of São Francisco Valley/BR