Evaluation of the modulation of nitric oxide synthase expression in the cerebellum of diabetic albino rats and the possible protective effect of ferulic acid
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作者:
Elhessy, Heba M.
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Mansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, EgyptMansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, Egypt
Elhessy, Heba M.
[1
]
Eltahry, Huda
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Mansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, EgyptMansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, Egypt
Eltahry, Huda
[1
]
Erfan, Omnia S.
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Mansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, EgyptMansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, Egypt
Erfan, Omnia S.
[1
]
Mahdi, Mohamed R.
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Mansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, EgyptMansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, Egypt
Mahdi, Mohamed R.
[1
]
Hazem, Noha M.
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Mansoura Univ, Fac Med, Dept Med Biochem, Mansoura, EgyptMansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, Egypt
Hazem, Noha M.
[2
]
El-Shahat, Mona A.
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Mansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, EgyptMansoura Univ, Fac Med, Dept Anat & Embryol, Mansoura, Egypt
Introduction: Diabetes mellitus is a multisystem disease. Oxidative stress and nitric oxide isoforms are involved in diabetic pathogenesis. Ferulic acid is a natural substance that is distributed broadly in plants with strong potent properties. The aim of the research: This research was designed to study the possible protective role of ferulic acid on oxidative stress and different Nitric oxide synthase isoforms (NOS) in the cerebellum of streptozotocin-induced diabetic rats. Materials and methods: Twenty-four albino male rats were randomly divided into equal four groups: control group, group 2 received ferulic acid orally (10 mg/kg), group 3 diabetic group, group 4 diabetic rats received ferulic acid. After 8 weeks, the left cerebellar hemisphere was taken for tissue homogenate for oxidative markers and real-time PCR for NOS isoforms. Paraffin sections of the right cerebellar hemisphere were stained with cresyl violet, Luxol fast blue and immnunohistochemically stained for neuronal NOS, inducible NOS and endothelial NOS. Results: Degenerative changes were seen in the cerebella of the diabetic rats with significant elevation of Malondialdehyde, Nitric Oxide, and decrease of Superoxide dismutase levels. nNOS expression decreased and iNOS expression increased significantly. The ferulic acid-treated group showed a reduction of the degenerative changes in the cerebellum with significant improvement in oxidative stress marker, an increase of nNOS expression, and a decrease of iNOS expression. Conclusions: Ferulic acid improves cerebellar functional and histopathological changes induced by diabetes which can be attributed mainly to its anti-oxidative effect and its ability to modulate NOS isoforms.
机构:
Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Poittevin, Marine
Bonnin, Philippe
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Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Hop Lariboisiere, AP HP, Serv Physiol Clin, F-75475 Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Bonnin, Philippe
Pimpie, Cynthia
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Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Pimpie, Cynthia
Riviere, Lea
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Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Riviere, Lea
Sebrie, Catherine
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Univ Paris 11, CNRS, UMR 8081, F-91405 Orsay, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Sebrie, Catherine
Dohan, Anthony
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Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Dohan, Anthony
Pocard, Marc
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Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Pocard, Marc
Charriaut-Marlangue, Christiane
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机构:
Univ Paris Diderot, Sorbonne Paris Cite, INSERM, U1141, Paris, France
DHU Protect, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Charriaut-Marlangue, Christiane
Kubis, Nathalie
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Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Hop Lariboisiere, AP HP, Serv Physiol Clin, F-75475 Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
机构:
Rockefeller Univ, Harold & Margaret Milliken hatch Lab Neuroendocri, New York, NY 10021 USARockefeller Univ, Harold & Margaret Milliken hatch Lab Neuroendocri, New York, NY 10021 USA
Reagan, LP
McEwen, BS
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Rockefeller Univ, Harold & Margaret Milliken hatch Lab Neuroendocri, New York, NY 10021 USARockefeller Univ, Harold & Margaret Milliken hatch Lab Neuroendocri, New York, NY 10021 USA
机构:
Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Poittevin, Marine
Bonnin, Philippe
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Hop Lariboisiere, AP HP, Serv Physiol Clin, F-75475 Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Bonnin, Philippe
Pimpie, Cynthia
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Pimpie, Cynthia
Riviere, Lea
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Riviere, Lea
Sebrie, Catherine
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris 11, CNRS, UMR 8081, F-91405 Orsay, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Sebrie, Catherine
Dohan, Anthony
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Dohan, Anthony
Pocard, Marc
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Pocard, Marc
Charriaut-Marlangue, Christiane
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris Diderot, Sorbonne Paris Cite, INSERM, U1141, Paris, France
DHU Protect, Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Charriaut-Marlangue, Christiane
Kubis, Nathalie
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
Hop Lariboisiere, AP HP, Serv Physiol Clin, F-75475 Paris, FranceUniv Paris Diderot, Sorbonne Paris Cite, Angiogenesis & Translat Res Ctr, INSERM,U965, Paris, France
机构:
Rockefeller Univ, Harold & Margaret Milliken hatch Lab Neuroendocri, New York, NY 10021 USARockefeller Univ, Harold & Margaret Milliken hatch Lab Neuroendocri, New York, NY 10021 USA
Reagan, LP
McEwen, BS
论文数: 0引用数: 0
h-index: 0
机构:
Rockefeller Univ, Harold & Margaret Milliken hatch Lab Neuroendocri, New York, NY 10021 USARockefeller Univ, Harold & Margaret Milliken hatch Lab Neuroendocri, New York, NY 10021 USA