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Toxicological evaluation of the biflavonoid, agathisflavone in albino Swiss mice.
Lopes Andrade, Anderson Wilbur; Dias Ribeiro Figueiredo, Daiana; Torequl Islam, Muhammad; Viana Nunes, Adriana Maria; da Conceição Machado, Keylla; da Conceição Machado, Katia; Uddin, Shaikh Jamal; Ahmed Shilpi, Jamil; Rouf, Razina; de Carvalho Melo-Cavalcante, Ana Amélia; David, Jorge Mauricio; Mubarak, Mohammad S; Pereira Costa, Jéssica.
Afiliación
  • Lopes Andrade AW; Laboratory of Research in Experimental Neurochemistry, Federal University of Piauí (UFPI), Teresina, Brazil.
  • Dias Ribeiro Figueiredo D; Chemistry Institute, Federal University of Bahia (UFBA), Salvador, Brazil.
  • Torequl Islam M; Department for Management of Science and Technology Development, Ton Duc Thang University, Ho Chi Minh City, Viet Nam; Faculty of Pharmacy, Ton Duc Thang University, Ho Chi Minh City, Viet Nam. Electronic address: muhammad.torequl.islam@tdtu.edu.vn.
  • Viana Nunes AM; Federal University of Piauí (UFPI), Teresina, Brazil.
  • da Conceição Machado K; Laboratory of Research in Experimental Neurochemistry, Federal University of Piauí (UFPI), Teresina, Brazil.
  • da Conceição Machado K; Laboratory of Research in Experimental Neurochemistry, Federal University of Piauí (UFPI), Teresina, Brazil.
  • Uddin SJ; Pharmacy Discipline, Life Science School, Khulna University, Khulna, Bangladesh.
  • Ahmed Shilpi J; Pharmacy Discipline, Life Science School, Khulna University, Khulna, Bangladesh.
  • Rouf R; Department of Pharmacy, Bangabandhu Sheikh Mujibur Rahman Science & Technology University, Gopalganj, Bangladesh.
  • de Carvalho Melo-Cavalcante AA; Laboratory of Research in Experimental Neurochemistry, Federal University of Piauí (UFPI), Teresina, Brazil.
  • David JM; Chemistry Institute, Federal University of Bahia (UFBA), Salvador, Brazil.
  • Mubarak MS; Department of Chemistry, The University of Jordan, Amman, 11942, Jordan. Electronic address: mmubarak@ju.edu.jo.
  • Pereira Costa J; Laboratory of Research in Experimental Neurochemistry, Federal University of Piauí (UFPI), Teresina, Brazil.
Biomed Pharmacother ; 110: 68-73, 2019 Feb.
Article en En | MEDLINE | ID: mdl-30466004
ABSTRACT
Agathisflavone (AGF) is a biflavonoid with a number of important biological and pharmacological activities, such as antioxidant, antimicrobial, and neuroprotective effects. However, its toxicological effects have not been fully investigated. Accordingly, the aim of this study was to investigate the toxicological effects of AGF in mice. For this purpose, the median lethal dose 50% (LD50) was determined along with the anatomic and histopathological parameters (weight, alimentation, excretion, biochemical, and hematological) in fertile untouched female Swiss mice. Results suggest that during the treatment, no deaths were reported at 300 and 2000 mg/kg (n = 03/group, p.o.). Moreover, AGF did not cause significant change in the above mentioned parameters in test animals when compared with the control group (0.05% Tween 80 dissolved in 0.9% saline). Taken all together, this non-clinical toxicological study revealed that AGF has an LD50 larger than 2000 mg/kg and did not change significantly the hematological, biochemical, histopathological, behavioral, as well as physiological parameters in the female mice.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Extractos Vegetales / Biflavonoides Límite: Animals Idioma: En Revista: Biomed Pharmacother Año: 2019 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Extractos Vegetales / Biflavonoides Límite: Animals Idioma: En Revista: Biomed Pharmacother Año: 2019 Tipo del documento: Article País de afiliación: Brasil
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