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Investigating the Protective Role of Vitamin D Supplementation on Cyclophosphamide-Induced Liver Enzyme Alterations in Adult Male Rats
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Abstract
Cyclophosphamide is known to cause liver dysfunction. This study investigated the
protective role of vitamin D supplementation against cyclophosphamide -induced
liver dysfunction in adult male rats. The rats receiving cyclophosphamide were
treated with vitamin D at doses of 1,000 and 3,000 IU/kg. At the end of the
study period, biochemical and histopathological evaluations were conducted after
the animals were sacrificed. The levels of aspartate aminotransferase, alanine
aminotransferase, alkaline phosphatase, lactate dehydrogenase, nitric oxide, and
bilirubin were significantly elevated in the cyclophosphamide group compared to
the control group (p<0.001). Conversely, these levels were
significantly decreased in the vitamin D treatment groups (p<0.01).
Additionally, the activities of the catalase and glutathione peroxidase were
significantly lower in the cyclophosphamide group than in controls
(p<0.01), while they increased significantly in the vitamin D groups
(p<0.001). According to a semi-quantitative scoring system, the
highest scores for pathological lesions were observed in the cyclophosphamide
group, with lower scores in the vitamin D groups. The differences between the
cyclophosphamide group and both treated groups were statistically significant
(p<0.05). These results indicate that vitamin D, through its
antioxidant properties, positively influenced liver enzyme levels altered by
cyclophosphamide.
Title: Investigating the Protective Role of Vitamin D Supplementation on
Cyclophosphamide-Induced Liver Enzyme Alterations in Adult Male
Rats
Description:
Abstract
Cyclophosphamide is known to cause liver dysfunction.
This study investigated the
protective role of vitamin D supplementation against cyclophosphamide -induced
liver dysfunction in adult male rats.
The rats receiving cyclophosphamide were
treated with vitamin D at doses of 1,000 and 3,000 IU/kg.
At the end of the
study period, biochemical and histopathological evaluations were conducted after
the animals were sacrificed.
The levels of aspartate aminotransferase, alanine
aminotransferase, alkaline phosphatase, lactate dehydrogenase, nitric oxide, and
bilirubin were significantly elevated in the cyclophosphamide group compared to
the control group (p<0.
001).
Conversely, these levels were
significantly decreased in the vitamin D treatment groups (p<0.
01).
Additionally, the activities of the catalase and glutathione peroxidase were
significantly lower in the cyclophosphamide group than in controls
(p<0.
01), while they increased significantly in the vitamin D groups
(p<0.
001).
According to a semi-quantitative scoring system, the
highest scores for pathological lesions were observed in the cyclophosphamide
group, with lower scores in the vitamin D groups.
The differences between the
cyclophosphamide group and both treated groups were statistically significant
(p<0.
05).
These results indicate that vitamin D, through its
antioxidant properties, positively influenced liver enzyme levels altered by
cyclophosphamide.
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