Startseite Toxicological evaluation of the lyophilized fruit juice extract of Annona muricata Linn. (Annonaceae) in rodents
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Toxicological evaluation of the lyophilized fruit juice extract of Annona muricata Linn. (Annonaceae) in rodents

  • Olufunsho Awodele EMAIL logo , Ismail O. Ishola , Victor O. Ikumawoyi , Abidemi J. Akindele und Alade Akintonwa
Veröffentlicht/Copyright: 18. Dezember 2013

Abstract

Background:Annona muricata Linn. (Annonaceae) (AM) fruit juice is widely consumed either raw or after processing in tropical countries because of its very juicy, creamy and sweet character including its medicinal importance. The safety of AM fruit was investigated in Sprague-Dawley rats for acute and 60-day subchronic toxicity effects.

Methods: Rats were administered distilled water (DW) and AM daily at doses of 80, 400 and 2000 mg/kg orally for 60 days. At the end of the study, blood samples were assayed for biochemical and hematological parameters. Vital organs were harvested and assessed for antioxidants and histopathology.

Results: There was no mortality recorded up to 2000 mg/kg following acute administration. There were no significant changes in vital organ weights and hematological and biochemical parameters. However, significant (p<0.05) reduction in platelet count and packed cell volume was observed at 2000 and 400 mg/kg, respectively, which was reversed after cessation of treatment. Interestingly, subchronic oral administration of AM (80, 400 or 2000 mg/kg) significantly (p<0.001) increased sperm count and motility in comparison to vehicle-treated control. AM long-term treatment induced significant (p<0.05, <0.01 and <0.001) increases in the levels of glutathione, superoxide dismutase (SOD) and catalase, respectively, in the liver and kidney. Conversely, AM (2000 mg/kg) produced significant (p<0.001) increase in malondialdehyde level with decreased (p<0.05) SOD activity in the brain.

Conclusions: The study established that AM did not induce any significant toxic effect, indicating that it is safe in rats following oral administration for 60 consecutive days.


Corresponding author: Olufunsho Awodele, Faculty of Basic Medical Sciences, Department of Pharmacology, College of Medicine, University of Lagos, Idi-Araba, Lagos, Nigeria, Phone: +2348023624044, E-mail: ;

Acknowledgments

The authors are grateful to Mr. S.O. Adenekan (Department of Biochemistry), Mr. M.C. Chijioke (Department of Pharmacology) and Dr. Orah Nnamdi (Department of Morbid Anatomy) of the Faculty of Basic Medical Sciences, College of Medicine, University of Lagos, Lagos, Nigeria, for technical assistance provided.

Conflict of interest statement

Authors’ conflict of interest disclosure: The authors stated that there are no conflicts of interest regarding the publication of this article.

Research funding: None declared.

Employment or leadership: None declared.

Honorarium: None declared.

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Received: 2013-7-1
Accepted: 2013-11-4
Published Online: 2013-12-18
Published in Print: 2014-11-1

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