Volume 34, Issue 12 e22584
RESEARCH ARTICLE

Effects of vitamin K dietary supplementation in pulmonary dysfunction induced by 7,12-dimethylbenz[a]anthracene in rat

Oluwatosin A. Dosumu,

Department of Biochemistry, Federal University of Agriculture, Abeokuta, Nigeria

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Solomon O. Rotimi,

Department of Biochemistry, Covenant University, Sango Ota, Nigeria

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Jacob Akintunde,

Department of Biochemistry, Federal University of Agriculture, Abeokuta, Nigeria

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Oluwagbemiga O. Adeleye,

Department of Animal Production and Health, Federal University of Agriculture, Abeokuta, Nigeria

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Latifah O. Sani,

Department of Biochemistry, Federal University of Agriculture, Abeokuta, Nigeria

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Oluwatosin O. Omotosho,

Department of Biochemistry, Federal University of Agriculture, Abeokuta, Nigeria

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Kehinde T. Osinuga,

Department of Biochemistry, Federal University of Agriculture, Abeokuta, Nigeria

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Odunayo A. Taiwo,

Corresponding Author

Department of Biochemistry, Federal University of Agriculture, Abeokuta, Nigeria

Department of Biochemistry, Chrisland University, Owode, Nigeria

Correspondence Odunayo A. Taiwo, Department of Biochemistry, Federal University of Agriculture, Abeokuta 110, Nigeria.

Email: odunayotaiwo25@gmail.com

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Oluwafemi A. Ojo,

Department of Biochemistry, Landmark University, Omu-Aran, Nigeria

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First published: 14 July 2020

Abstract

One of the well-known toxicants of the mammary tissue is 7,12-dimethylbenz[a]anthracene (DMBA). This study was carried out to investigate the possible prophylactic's role of increased dietary intake of vitamin K on the induction of toxicity in the lung tissue. Twenty-eight Wistar albino rats (120-150 g) were randomly divided into different groups. Group 1 served as the control and were fed with a normal diet (containing the recommended daily allowance of vitamin K (0.0075%)). Groups 2 and 3 received a single dose of DMBA (80 mg/kg body weight) intragastically. In addition, group 3 rats were maintained on surplus vitamin K diet (0.075% diet) as against the group 2 animals that were on a normal diet. Group 4 rats were on surplus vitamin K diet (0.075% diet) throughout the experimental period of 16 weeks. Our results revealed that supplementation of diet with surplus vitamin K significantly increased the activities of catalase. Superoxide dismutase, glutathione-S-transferase, and glutathione peroxidase were significantly increased in the serum and lungs when compared with the DMBA-treated group, which was maintained on a normal diet. Significant alterations in malondialdehyde, nitric oxide, granulocyte-macrophage colony-stimulating factor, and interleukin 17F were observed in rats challenged with DMBA-fed normal diets but were normalized in rats with surplus vitamin K. These alterations and reversal were confirmed by histopathology studies. This suggests the prophylactic benefit of increased dietary intake of vitamin K without any observed deleterious effect on DMBA-induced pulmonary toxicity.

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