Evelyne da Silva Brum1, Laís da Rosa Moreira1, Andreia Regina Haas da Silva2, Aline Augusti Boligon3, Fabiano Barbosa Carvalho4, Margareth Linde Athayde3, Ricardo Brandão2, Sara Marchesan Oliveira5. 1. Laboratory of Neurotoxicity and Psychopharmacology, Center of Natural and Exact Sciences, Federal University of Santa Maria, Santa Maria, RS, Brazil. 2. Laboratory of Toxicological Analysis, Pharmaceutical Sciences Graduate Program, Center of Health Sciences, Federal University of Santa Maria, Santa Maria, RS, Brazil. 3. Laboratory of Phytochemistry, Pharmaceutical Sciences Graduate Program, Center of Health Sciences, Federal University of Santa Maria, Santa Maria, RS, Brazil. 4. Department of Biochemistry and Molecular Biology, Graduate Program in Biological Sciences: Biochemical Toxicology, Center of Natural and Exact Sciences, Federal University of Santa Maria, Santa Maria, RS, Brazil. 5. Laboratory of Neurotoxicity and Psychopharmacology, Center of Natural and Exact Sciences, Federal University of Santa Maria, Santa Maria, RS, Brazil; Department of Biochemistry and Molecular Biology, Graduate Program in Biological Sciences: Biochemical Toxicology, Center of Natural and Exact Sciences, Federal University of Santa Maria, Santa Maria, RS, Brazil. Electronic address: saramarchesan@hotmail.com.
Abstract
ETHNOPHARMACOLOGICAL RELEVANCE: Tabernaemontana catharinensis (Apocynaceae) is a medicinal plant used for the treatment of painful and inflammatory disorders. Here, we investigated the antinociceptive potential of the ethyl acetate fraction (Eta) from T. catharinensis leaves and assessed its toxic effects in mice to validate its popular use. MATERIALS AND METHODS: Adult male Swiss mice (30-35g) were used. The Eta antinociceptive effect (200-800mg/kg, oral route (p.o.)) was evaluated in the acetic acid, formalin, capsaicin and tail-immersion tests. Adverse effects were analyzed using rotarod and open-field tests, body temperature, biochemical analysis and gastric lesions assessment. To evaluate the acute (OECD 423) or sub-acute (OECD 407) toxicity of the Eta, it was administered orally at a single (2000mg/kg) or repeated doses (100-400mg/kg/day for 28 days), respectively. Mortality, behavioral changes, biochemical and hematological parameters were evaluated. The Eta effect on cellular viability also was evaluated. RESULTS: Eta (200-800mg/kg) inhibited the nociception caused by acetic acid (93.9±1.5%), formalin (86.2±10.8%) or capsaicin (75.4±3.3%) without inducing gastric lesions. Moreover, Eta neither altered the body temperature, biochemical parameters, nor forced or spontaneous locomotor activity of mice. The acute administration of the Eta (2000mg/kg) promoted a decrease in blood glucose levels and alanine aminotransferase activity. In the sub-acute toxicity study, Eta increased the aspartate aminotransferase activity (400mg/kg) and platelet distribution width (200mg/kg). Furthermore, Eta did not alter the cellular viability in cortical slices. CONCLUSIONS: Eta presents antinociceptive effects and mild toxicity in mice. These results support its traditional use as a potential analgesic.
ETHNOPHARMACOLOGICAL RELEVANCE: Tabernaemontana catharinensis (Apocynaceae) is a medicinal plant used for the treatment of painful and inflammatory disorders. Here, we investigated the antinociceptive potential of the ethyl acetate fraction (Eta) from T. catharinensis leaves and assessed its toxic effects in mice to validate its popular use. MATERIALS AND METHODS: Adult male Swiss mice (30-35g) were used. The Eta antinociceptive effect (200-800mg/kg, oral route (p.o.)) was evaluated in the acetic acid, formalin, capsaicin and tail-immersion tests. Adverse effects were analyzed using rotarod and open-field tests, body temperature, biochemical analysis and gastric lesions assessment. To evaluate the acute (OECD 423) or sub-acute (OECD 407) toxicity of the Eta, it was administered orally at a single (2000mg/kg) or repeated doses (100-400mg/kg/day for 28 days), respectively. Mortality, behavioral changes, biochemical and hematological parameters were evaluated. The Eta effect on cellular viability also was evaluated. RESULTS: Eta (200-800mg/kg) inhibited the nociception caused by acetic acid (93.9±1.5%), formalin (86.2±10.8%) or capsaicin (75.4±3.3%) without inducing gastric lesions. Moreover, Eta neither altered the body temperature, biochemical parameters, nor forced or spontaneous locomotor activity of mice. The acute administration of the Eta (2000mg/kg) promoted a decrease in blood glucose levels and alanine aminotransferase activity. In the sub-acute toxicity study, Eta increased the aspartate aminotransferase activity (400mg/kg) and platelet distribution width (200mg/kg). Furthermore, Eta did not alter the cellular viability in cortical slices. CONCLUSIONS: Eta presents antinociceptive effects and mild toxicity in mice. These results support its traditional use as a potential analgesic.
Authors: Neida L Pellenz; Fernanda Barbisan; Veronica F Azzolin; Thiago Duarte; Aline Bolignon; Moisés H Mastella; Cibele F Teixeira; Euler E Ribeiro; Ivana B Mânica da Cruz; Marta M M F Duarte Journal: Biomed Res Int Date: 2018-10-08 Impact factor: 3.411