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Inhibition of gene expression of organic cation/carnitine transporter and antioxidant enzymes in oxazaphosphorines-induced acute cardiomyopathic rat models.

Sayed-Ahmed MM, Aldelemy ML, Hafez MM, Al-Shabanah OA - Oxid Med Cell Longev (2012)

Bottom Line: It is well documented that high therapeutic doses of oxazaphosphorines, cyclophosphamide (CP) and ifosfamide (IFO), are associated with cardiomyopathy.In cardiac and kidney tissues, CP and IFO significantly decreased mRNA and protein expression of OCTN2.Data from this study suggest that: (1) Oxazaphosphorines decreased myocardial carnitine content following the inhibition of OCTN2 mRNA and protein expression in cardiac tissues. (2) Oxazaphosphorine therapy increased urinary loss of carnitine secondary to the inhibition of OCTN2 mRNA and protein expression in proximal tubules of the kidney. (3) Carnitine supplementation attenuates CP but not IFO-induced inhibition of OCTN2 mRNA and protein expression in heart and kidney tissues.

View Article: PubMed Central - PubMed

Affiliation: Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia. sayedahmedmm@hotmail.com

ABSTRACT
It is well documented that high therapeutic doses of oxazaphosphorines, cyclophosphamide (CP) and ifosfamide (IFO), are associated with cardiomyopathy. This study investigated whether oxazaphosphorines alter the expression of organic cation/carnitine transporter (OCTN2) and antioxidant genes and if so, whether these alterations contribute to CP and IFO-induced cardiotoxicity. Adult male Wistar albino rats were assigned to one of six treatment groups namely, control, L carnitine, CP, IFO, CP plus L carnitine and IFO plus L carnitine. In cardiac and kidney tissues, CP and IFO significantly decreased mRNA and protein expression of OCTN2. Oxazaphosphorines significantly increased serum acyl-carnitine/free carnitine ratio and urinary carnitine excretion and significantly decreased total carnitine in cardiac tissues. Interestingly, carnitine supplementation completely reversed the biochemical and gene expression changes-induced by oxazaphosphorines to the control values, except OCTN2 expression remained inhibited by IFO. Data from this study suggest that: (1) Oxazaphosphorines decreased myocardial carnitine content following the inhibition of OCTN2 mRNA and protein expression in cardiac tissues. (2) Oxazaphosphorine therapy increased urinary loss of carnitine secondary to the inhibition of OCTN2 mRNA and protein expression in proximal tubules of the kidney. (3) Carnitine supplementation attenuates CP but not IFO-induced inhibition of OCTN2 mRNA and protein expression in heart and kidney tissues.

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Effects of cyclophosphamide (CP), ifosfamide (IFO), L carnitine (LC), and their combination on serum cardiotoxicity enzymatic indices, CK-MB (a) and LDH (b), in rats. Rats were randomly divided into 6 different groups of 10 animals each: control, L carnitine, CP, IFO, CP carnitine supplemented and IFO carnitine supplemented. Carnitine supplementation was induced in rats by daily intraperitoneal injection of L carnitine (200 mg/kg/day) for 10 successive days. CP cardiotoxicity was induced in rats by administration of a single dose of CP (200 mg/kg). IFO cardiotoxicity was induced in rats by administration of IFO (50 mg/kg/day, I.P.) for 5 successive days. CP-carnitine supplemented rats were given the same doses of L carnitine (200 mg/kg/day) for 5 days before and 5 days after a single dose of CP (200 mg/kg). IFO-carnitine-supplemented rats were given the same doses of L carnitine (200 mg/kg/day) for 5 days before and 5 days concomitant with IFO (50 mg/kg/day, I.P.). At the end of the treatment protocol, cardiac enzymes were measured in serum. Data are presented as mean ± S.E.M. (n = 10). *, #, and $ indicate significant change from control, CP and IFO, respectively, at P < 0.05 using ANOVA followed by Tukey-Kramer as a post-ANOVA test.
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fig1: Effects of cyclophosphamide (CP), ifosfamide (IFO), L carnitine (LC), and their combination on serum cardiotoxicity enzymatic indices, CK-MB (a) and LDH (b), in rats. Rats were randomly divided into 6 different groups of 10 animals each: control, L carnitine, CP, IFO, CP carnitine supplemented and IFO carnitine supplemented. Carnitine supplementation was induced in rats by daily intraperitoneal injection of L carnitine (200 mg/kg/day) for 10 successive days. CP cardiotoxicity was induced in rats by administration of a single dose of CP (200 mg/kg). IFO cardiotoxicity was induced in rats by administration of IFO (50 mg/kg/day, I.P.) for 5 successive days. CP-carnitine supplemented rats were given the same doses of L carnitine (200 mg/kg/day) for 5 days before and 5 days after a single dose of CP (200 mg/kg). IFO-carnitine-supplemented rats were given the same doses of L carnitine (200 mg/kg/day) for 5 days before and 5 days concomitant with IFO (50 mg/kg/day, I.P.). At the end of the treatment protocol, cardiac enzymes were measured in serum. Data are presented as mean ± S.E.M. (n = 10). *, #, and $ indicate significant change from control, CP and IFO, respectively, at P < 0.05 using ANOVA followed by Tukey-Kramer as a post-ANOVA test.

Mentions: Figure 1 shows the effects of oxazaphosphorines, L carnitine, and their combination on cardiotoxicity enzymatic indices, CK-MB (a) and LDH (b), in rats. Administration of a single dose of CP (200 mg/kg) resulted in a significant 77 and 92% increase in serum CK-MB and LDH, respectively, as compared to the control group. Treatment with L carnitine (200 mg/kg/day) for 10 successive days showed non significant changes. Interestingly, administration of L carnitine for 5 days before and 5 days after a single dose of CP resulted in a complete reversal of CP-induced increase in serum CK-MB and LDH to the control values. On the other hand, administration of IFO (50 mg/kg/day) for 5 successive days resulted in 52 and 67% increase in serum CK-MB and LDH, respectively, as compared to the control group. Carnitine supplementation by daily administration of L carnitine for 5 days before and 5 days concomitant with IFO resulted in a complete reversal of IFO-induced increase in serum CK-MB and LDH to the control values.


Inhibition of gene expression of organic cation/carnitine transporter and antioxidant enzymes in oxazaphosphorines-induced acute cardiomyopathic rat models.

Sayed-Ahmed MM, Aldelemy ML, Hafez MM, Al-Shabanah OA - Oxid Med Cell Longev (2012)

Effects of cyclophosphamide (CP), ifosfamide (IFO), L carnitine (LC), and their combination on serum cardiotoxicity enzymatic indices, CK-MB (a) and LDH (b), in rats. Rats were randomly divided into 6 different groups of 10 animals each: control, L carnitine, CP, IFO, CP carnitine supplemented and IFO carnitine supplemented. Carnitine supplementation was induced in rats by daily intraperitoneal injection of L carnitine (200 mg/kg/day) for 10 successive days. CP cardiotoxicity was induced in rats by administration of a single dose of CP (200 mg/kg). IFO cardiotoxicity was induced in rats by administration of IFO (50 mg/kg/day, I.P.) for 5 successive days. CP-carnitine supplemented rats were given the same doses of L carnitine (200 mg/kg/day) for 5 days before and 5 days after a single dose of CP (200 mg/kg). IFO-carnitine-supplemented rats were given the same doses of L carnitine (200 mg/kg/day) for 5 days before and 5 days concomitant with IFO (50 mg/kg/day, I.P.). At the end of the treatment protocol, cardiac enzymes were measured in serum. Data are presented as mean ± S.E.M. (n = 10). *, #, and $ indicate significant change from control, CP and IFO, respectively, at P < 0.05 using ANOVA followed by Tukey-Kramer as a post-ANOVA test.
© Copyright Policy - open-access
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC3369488&req=5

fig1: Effects of cyclophosphamide (CP), ifosfamide (IFO), L carnitine (LC), and their combination on serum cardiotoxicity enzymatic indices, CK-MB (a) and LDH (b), in rats. Rats were randomly divided into 6 different groups of 10 animals each: control, L carnitine, CP, IFO, CP carnitine supplemented and IFO carnitine supplemented. Carnitine supplementation was induced in rats by daily intraperitoneal injection of L carnitine (200 mg/kg/day) for 10 successive days. CP cardiotoxicity was induced in rats by administration of a single dose of CP (200 mg/kg). IFO cardiotoxicity was induced in rats by administration of IFO (50 mg/kg/day, I.P.) for 5 successive days. CP-carnitine supplemented rats were given the same doses of L carnitine (200 mg/kg/day) for 5 days before and 5 days after a single dose of CP (200 mg/kg). IFO-carnitine-supplemented rats were given the same doses of L carnitine (200 mg/kg/day) for 5 days before and 5 days concomitant with IFO (50 mg/kg/day, I.P.). At the end of the treatment protocol, cardiac enzymes were measured in serum. Data are presented as mean ± S.E.M. (n = 10). *, #, and $ indicate significant change from control, CP and IFO, respectively, at P < 0.05 using ANOVA followed by Tukey-Kramer as a post-ANOVA test.
Mentions: Figure 1 shows the effects of oxazaphosphorines, L carnitine, and their combination on cardiotoxicity enzymatic indices, CK-MB (a) and LDH (b), in rats. Administration of a single dose of CP (200 mg/kg) resulted in a significant 77 and 92% increase in serum CK-MB and LDH, respectively, as compared to the control group. Treatment with L carnitine (200 mg/kg/day) for 10 successive days showed non significant changes. Interestingly, administration of L carnitine for 5 days before and 5 days after a single dose of CP resulted in a complete reversal of CP-induced increase in serum CK-MB and LDH to the control values. On the other hand, administration of IFO (50 mg/kg/day) for 5 successive days resulted in 52 and 67% increase in serum CK-MB and LDH, respectively, as compared to the control group. Carnitine supplementation by daily administration of L carnitine for 5 days before and 5 days concomitant with IFO resulted in a complete reversal of IFO-induced increase in serum CK-MB and LDH to the control values.

Bottom Line: It is well documented that high therapeutic doses of oxazaphosphorines, cyclophosphamide (CP) and ifosfamide (IFO), are associated with cardiomyopathy.In cardiac and kidney tissues, CP and IFO significantly decreased mRNA and protein expression of OCTN2.Data from this study suggest that: (1) Oxazaphosphorines decreased myocardial carnitine content following the inhibition of OCTN2 mRNA and protein expression in cardiac tissues. (2) Oxazaphosphorine therapy increased urinary loss of carnitine secondary to the inhibition of OCTN2 mRNA and protein expression in proximal tubules of the kidney. (3) Carnitine supplementation attenuates CP but not IFO-induced inhibition of OCTN2 mRNA and protein expression in heart and kidney tissues.

View Article: PubMed Central - PubMed

Affiliation: Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia. sayedahmedmm@hotmail.com

ABSTRACT
It is well documented that high therapeutic doses of oxazaphosphorines, cyclophosphamide (CP) and ifosfamide (IFO), are associated with cardiomyopathy. This study investigated whether oxazaphosphorines alter the expression of organic cation/carnitine transporter (OCTN2) and antioxidant genes and if so, whether these alterations contribute to CP and IFO-induced cardiotoxicity. Adult male Wistar albino rats were assigned to one of six treatment groups namely, control, L carnitine, CP, IFO, CP plus L carnitine and IFO plus L carnitine. In cardiac and kidney tissues, CP and IFO significantly decreased mRNA and protein expression of OCTN2. Oxazaphosphorines significantly increased serum acyl-carnitine/free carnitine ratio and urinary carnitine excretion and significantly decreased total carnitine in cardiac tissues. Interestingly, carnitine supplementation completely reversed the biochemical and gene expression changes-induced by oxazaphosphorines to the control values, except OCTN2 expression remained inhibited by IFO. Data from this study suggest that: (1) Oxazaphosphorines decreased myocardial carnitine content following the inhibition of OCTN2 mRNA and protein expression in cardiac tissues. (2) Oxazaphosphorine therapy increased urinary loss of carnitine secondary to the inhibition of OCTN2 mRNA and protein expression in proximal tubules of the kidney. (3) Carnitine supplementation attenuates CP but not IFO-induced inhibition of OCTN2 mRNA and protein expression in heart and kidney tissues.

Show MeSH
Related in: MedlinePlus