Sesamin modulates tyrosine hydroxylase, superoxide dismutase, catalase, inducible NO synthase and interleukin-6 expression in dopaminergic cells under MPP+-induced oxidative stress
Identifieur interne : 002144 ( Main/Exploration ); précédent : 002143; suivant : 002145Sesamin modulates tyrosine hydroxylase, superoxide dismutase, catalase, inducible NO synthase and interleukin-6 expression in dopaminergic cells under MPP+-induced oxidative stress
Auteurs : Vicky Lahaie-Collins ; Julie Bournival ; Marilyn Plouffe ; Julie Carange ; Maria-Grazia MartinoliSource :
- Oxidative Medicine and Cellular Longevity [ 1942-0900 ] ; 2008.
English descriptors
- KwdEn :
- 1-Methyl-4-phenylpyridinium (pharmacology), Animals, Antioxidants (pharmacology), Catalase (biosynthesis), Catalase (metabolism), Dioxoles (pharmacology), Dopamine (metabolism), Dopamine Plasma Membrane Transport Proteins (metabolism), Interleukin-6 (biosynthesis), Interleukin-6 (metabolism), Lignans (pharmacology), Neurons (drug effects), Neurons (enzymology), Neurons (metabolism), Nitric Oxide Synthase Type II (biosynthesis), Nitric Oxide Synthase Type II (metabolism), Oxidative Stress (drug effects), Oxidative Stress (physiology), PC12 Cells, Rats, Reactive Oxygen Species (metabolism), Superoxide Dismutase (biosynthesis), Superoxide Dismutase (metabolism), Tyrosine 3-Monooxygenase (biosynthesis), Tyrosine 3-Monooxygenase (metabolism).
- MESH :
- chemical , biosynthesis : Catalase, Interleukin-6, Nitric Oxide Synthase Type II, Superoxide Dismutase, Tyrosine 3-Monooxygenase.
- chemical , metabolism : Catalase, Dopamine, Dopamine Plasma Membrane Transport Proteins, Interleukin-6, Nitric Oxide Synthase Type II, Reactive Oxygen Species, Superoxide Dismutase, Tyrosine 3-Monooxygenase.
- chemical , pharmacology : 1-Methyl-4-phenylpyridinium, Antioxidants, Dioxoles, Lignans.
- drug effects : Neurons, Oxidative Stress.
- enzymology : Neurons.
- metabolism : Neurons.
- physiology : Oxidative Stress.
- Animals, PC12 Cells, Rats.
Abstract
Oxidative stress is regarded as a mediator of nerve cell death in several neurodegenerative disorders, such as Parkinson's disease. Sesamin, a lignan mainly found in sesame oil, is currently under study for its anti-oxidative and possible neuroprotective properties. We used 1-methyl-4-phenyl-pyridine (MPP+) ion, the active metabolite of the potent parkinsonism-causing toxin 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine, to produce oxidative stress and neurodegeneration in neuronal PC12 cells, which express dopamine, as well as neurofilaments. Our results show that picomolar doses of sesamin protected neuronal PC12 cells from MPP+-induced cellular death, as revealed by colorimetric measurements and production of reactive oxygen species. We also demonstrated that sesamin acted by rescuing tyrosine hydroxylase levels from MPP+-induced depletion. Sesamin, however, did not modulate dopamine transporter levels, and estrogen receptor-alpha and -beta protein expression. By examining several parameters of cell distress, we found that sesamin also elicited a strong increase in superoxide dismutase activity as well as protein expression and decreased catalase activity and the MPP+ stimulated inducible nitric oxide synthase protein expression, in neuronal PC12 cells. Finally, sesamin possessed significant anti-inflammatory properties, as disclosed by its potential to reduce MPP+-induced interleukin-6 mRNA levels in microglia. From these studies, we determined the importance of the lignan sesamin as a neuroprotective molecule and its possible role in complementary and/or preventive therapies of neurodegenerative diseases.
Url:
PubMed: 19794909
PubMed Central: 2715194
Affiliations:
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Le document en format XML
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<author><name sortKey="Lahaie Collins, Vicky" sort="Lahaie Collins, Vicky" uniqKey="Lahaie Collins V" first="Vicky" last="Lahaie-Collins">Vicky Lahaie-Collins</name>
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<term>Antioxidants (pharmacology)</term>
<term>Catalase (biosynthesis)</term>
<term>Catalase (metabolism)</term>
<term>Dioxoles (pharmacology)</term>
<term>Dopamine (metabolism)</term>
<term>Dopamine Plasma Membrane Transport Proteins (metabolism)</term>
<term>Interleukin-6 (biosynthesis)</term>
<term>Interleukin-6 (metabolism)</term>
<term>Lignans (pharmacology)</term>
<term>Neurons (drug effects)</term>
<term>Neurons (enzymology)</term>
<term>Neurons (metabolism)</term>
<term>Nitric Oxide Synthase Type II (biosynthesis)</term>
<term>Nitric Oxide Synthase Type II (metabolism)</term>
<term>Oxidative Stress (drug effects)</term>
<term>Oxidative Stress (physiology)</term>
<term>PC12 Cells</term>
<term>Rats</term>
<term>Reactive Oxygen Species (metabolism)</term>
<term>Superoxide Dismutase (biosynthesis)</term>
<term>Superoxide Dismutase (metabolism)</term>
<term>Tyrosine 3-Monooxygenase (biosynthesis)</term>
<term>Tyrosine 3-Monooxygenase (metabolism)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Catalase</term>
<term>Interleukin-6</term>
<term>Nitric Oxide Synthase Type II</term>
<term>Superoxide Dismutase</term>
<term>Tyrosine 3-Monooxygenase</term>
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<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Catalase</term>
<term>Dopamine</term>
<term>Dopamine Plasma Membrane Transport Proteins</term>
<term>Interleukin-6</term>
<term>Nitric Oxide Synthase Type II</term>
<term>Reactive Oxygen Species</term>
<term>Superoxide Dismutase</term>
<term>Tyrosine 3-Monooxygenase</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>1-Methyl-4-phenylpyridinium</term>
<term>Antioxidants</term>
<term>Dioxoles</term>
<term>Lignans</term>
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<term>Oxidative Stress</term>
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<front><div type="abstract" xml:lang="en"><p>Oxidative stress is regarded as a mediator of nerve cell death in several neurodegenerative disorders, such as Parkinson's disease. Sesamin, a lignan mainly found in sesame oil, is currently under study for its anti-oxidative and possible neuroprotective properties. We used 1-methyl-4-phenyl-pyridine (MPP<sup>+</sup>
) ion, the active metabolite of the potent parkinsonism-causing toxin 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine, to produce oxidative stress and neurodegeneration in neuronal PC12 cells, which express dopamine, as well as neurofilaments. Our results show that picomolar doses of sesamin protected neuronal PC12 cells from MPP<sup>+</sup>
-induced cellular death, as revealed by colorimetric measurements and production of reactive oxygen species. We also demonstrated that sesamin acted by rescuing tyrosine hydroxylase levels from MPP<sup>+</sup>
-induced depletion. Sesamin, however, did not modulate dopamine transporter levels, and estrogen receptor-alpha and -beta protein expression. By examining several parameters of cell distress, we found that sesamin also elicited a strong increase in superoxide dismutase activity as well as protein expression and decreased catalase activity and the MPP<sup>+</sup>
stimulated inducible nitric oxide synthase protein expression, in neuronal PC12 cells. Finally, sesamin possessed significant anti-inflammatory properties, as disclosed by its potential to reduce MPP<sup>+</sup>
-induced interleukin-6 mRNA levels in microglia. From these studies, we determined the importance of the lignan sesamin as a neuroprotective molecule and its possible role in complementary and/or preventive therapies of neurodegenerative diseases.</p>
</div>
</front>
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<tree><noCountry><name sortKey="Bournival, Julie" sort="Bournival, Julie" uniqKey="Bournival J" first="Julie" last="Bournival">Julie Bournival</name>
<name sortKey="Carange, Julie" sort="Carange, Julie" uniqKey="Carange J" first="Julie" last="Carange">Julie Carange</name>
<name sortKey="Lahaie Collins, Vicky" sort="Lahaie Collins, Vicky" uniqKey="Lahaie Collins V" first="Vicky" last="Lahaie-Collins">Vicky Lahaie-Collins</name>
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