Changes in biochemical parameters in rabbits blood after oral exposure to diphenyl diselenide for long periods

The concept that selenium-containing molecules may be better antioxidants than classical antioxidants, has led to the design of synthetic organoselenium compounds. The present study was conducted to evaluate the potential toxicity of long time oral exposure to diphenyl diselenide (PhSe)2 in rabbits....

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Published inChemico-biological interactions Vol. 162; no. 1; pp. 1 - 10
Main Authors de Bem, Andreza Fabro, de Lima Portella, Rafael, Perottoni, Juliano, Becker, Emilene, Bohrer, Denise, Paixão, Márcio Weber, Nogueira, Cristina Wayne, Zeni, Gilson, Rocha, João Batista Teixeira
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Published Ireland 25.07.2006
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Abstract The concept that selenium-containing molecules may be better antioxidants than classical antioxidants, has led to the design of synthetic organoselenium compounds. The present study was conducted to evaluate the potential toxicity of long time oral exposure to diphenyl diselenide (PhSe)2 in rabbits. Male adult New Zealand rabbits were divided into four groups, group I served as control; groups II, III and IV received 0.3, 3.0 and 30 ppm of (PhSe)2 pulverized in the chow for 8 months. A number of parameters were examined in blood as indicators of toxicity, including delta-aminolevulinate dehydratase (delta-ALA-D), catalase, glutathione peroxidase (GPx), alanine aminotransferase (ALT), aspartate aminotransferase (AST), urea, creatinine, TBARS, non-protein-SH, ascorbic acid and selenium. The results demonstrated that 6 and 8 months of 30 ppm (PhSe)2 intake caused a significant increase in blood delta-ALA-D activity. Erythrocyte non-protein thiol levels were significantly increased after 2 months of 30 ppm (PhSe)2 intake and then return to control levels after prolonged periods of intake. Ingestion of 3.0 ppm of (PhSe)2 for 8 months significantly increased catalase activity in erythrocytes. Conversely, no alterations in GPx, ALT, AST, TBARS and selenium levels were observed in rabbit serum, conversely, selenium levels in peri-renal adipose tissue were significantly increased after 8 months of 30 ppm (PhSe)2 intake, indicating its great lipophylicity. The present results suggest that diphenyl diselenide was not hepato- or renotoxic for rabbits, but caused some biochemical alterations that can be related to some pro-oxidant activity of the compound (particularly the reduction in Vitamin C).
AbstractList The concept that selenium-containing molecules may be better antioxidants than classical antioxidants, has led to the design of synthetic organoselenium compounds. The present study was conducted to evaluate the potential toxicity of long time oral exposure to diphenyl diselenide (PhSe) sub(2) in rabbits. Male adult New Zealand rabbits were divided into four groups, group I served as control; groups II, III and IV received 0.3, 3.0 and 30 ppm of (PhSe) sub(2) pulverized in the ohow for 8 months. A number of parameters were examined in blood as indicators of toxicity, incluited by aminolevulinate dehydratase ( delta -ALA-D), catalase, glutathione peroxidase (GPx), alanine aminotransferase (ALT), aspartate aminotransferase (AST), urea, creatinine, TBARS, non-protein-SH, ascorbic acid and selenium. The results demonstrated that 6 and 8 months of 30 ppm (PhSe) sub(2) intake caused a significant increase in blood delta -ALA-D activity. Erythrocyte non-protein thiol levels were significantly increased after 2 months of 30 ppm (PhSe) sub(2) intake and then return to control levels after prolonged periods of intake. Ingestjon of 3.0 ppm of (PhSe) sub(2) for 8 months significantly increased catalase activity in erythrocytes. Conversely, no alterations in GPx, ALT, AST, TBARS and selenium levels were observed in rabbit serum, conversely, selenium levels in peri-renal adipose tissue were significantly increased after 8 months of 30 ppm (PhSe) sub(2) intake, indicating its great lipophylicity. The present results suggest that diphenyl diselenide was not hepato- or renotoxic for rabbits, but caused some biochemical alterations that can be related to some pro-oxidant activity of the compound (particularly the reduction in Vitamin C).
The concept that selenium-containing molecules may be better antioxidants than classical antioxidants, has led to the design of synthetic organoselenium compounds. The present study was conducted to evaluate the potential toxicity of long time oral exposure to diphenyl diselenide (PhSe)2 in rabbits. Male adult New Zealand rabbits were divided into four groups, group I served as control; groups II, III and IV received 0.3, 3.0 and 30 ppm of (PhSe)2 pulverized in the chow for 8 months. A number of parameters were examined in blood as indicators of toxicity, including delta-aminolevulinate dehydratase (delta-ALA-D), catalase, glutathione peroxidase (GPx), alanine aminotransferase (ALT), aspartate aminotransferase (AST), urea, creatinine, TBARS, non-protein-SH, ascorbic acid and selenium. The results demonstrated that 6 and 8 months of 30 ppm (PhSe)2 intake caused a significant increase in blood delta-ALA-D activity. Erythrocyte non-protein thiol levels were significantly increased after 2 months of 30 ppm (PhSe)2 intake and then return to control levels after prolonged periods of intake. Ingestion of 3.0 ppm of (PhSe)2 for 8 months significantly increased catalase activity in erythrocytes. Conversely, no alterations in GPx, ALT, AST, TBARS and selenium levels were observed in rabbit serum, conversely, selenium levels in peri-renal adipose tissue were significantly increased after 8 months of 30 ppm (PhSe)2 intake, indicating its great lipophylicity. The present results suggest that diphenyl diselenide was not hepato- or renotoxic for rabbits, but caused some biochemical alterations that can be related to some pro-oxidant activity of the compound (particularly the reduction in Vitamin C).
Author de Lima Portella, Rafael
de Bem, Andreza Fabro
Perottoni, Juliano
Becker, Emilene
Nogueira, Cristina Wayne
Rocha, João Batista Teixeira
Paixão, Márcio Weber
Bohrer, Denise
Zeni, Gilson
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  surname: Perottoni
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  organization: Departamento de Química, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, RS 97105900, Brazil
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  givenname: Emilene
  surname: Becker
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  givenname: Cristina Wayne
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  givenname: João Batista Teixeira
  surname: Rocha
  fullname: Rocha, João Batista Teixeira
  email: jbtrocha@yahoo.com.br
  organization: Departamento de Química, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, RS 97105900, Brazil. Electronic address: jbtrocha@yahoo.com.br
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Snippet The concept that selenium-containing molecules may be better antioxidants than classical antioxidants, has led to the design of synthetic organoselenium...
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StartPage 1
SubjectTerms Administration, Oral
Animal Feed
Animals
Ascorbic Acid - blood
Benzene Derivatives - administration & dosage
Benzene Derivatives - chemistry
Benzene Derivatives - pharmacology
Blood - drug effects
Blood - metabolism
Body Weight - drug effects
Catalase - metabolism
Creatinine - urine
Glutathione Peroxidase - metabolism
Male
Molecular Structure
Organoselenium Compounds - administration & dosage
Organoselenium Compounds - chemistry
Organoselenium Compounds - pharmacology
Porphobilinogen Synthase - metabolism
Rabbits
Selenium - metabolism
Sulfhydryl Compounds - metabolism
Thiobarbituric Acid Reactive Substances - metabolism
Time Factors
Title Changes in biochemical parameters in rabbits blood after oral exposure to diphenyl diselenide for long periods
URI https://www.ncbi.nlm.nih.gov/pubmed/16737689
https://search.proquest.com/docview/20377162
Volume 162
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