Anti-inflammatory effects of Citrus sinensis L., Citrus paradisi L. and their combinations.
Identifieur interne : 000335 ( Main/Exploration ); précédent : 000334; suivant : 000336Anti-inflammatory effects of Citrus sinensis L., Citrus paradisi L. and their combinations.
Auteurs : Rafeeq Alam Khan [Pakistan] ; Neelam Mallick [Pakistan] ; Zeeshan FerozSource :
- Pakistan journal of pharmaceutical sciences [ 1011-601X ] ; 2016.
English descriptors
- KwdEn :
- Alkaline Phosphatase (metabolism), Animals, Anti-Inflammatory Agents (isolation & purification), Anti-Inflammatory Agents (pharmacology), Antioxidants (isolation & purification), Antioxidants (pharmacology), Biomarkers (metabolism), C-Reactive Protein (metabolism), Citrus paradisi (chemistry), Citrus sinensis (chemistry), Colitis (chemically induced), Colitis (metabolism), Colitis (pathology), Colitis (prevention & control), Colon (drug effects), Colon (metabolism), Colon (pathology), Disease Models, Animal, Dose-Response Relationship, Drug, Drug Therapy, Combination, Fruit, Fruit and Vegetable Juices, Glutathione (metabolism), Inflammation Mediators (metabolism), Male, Oxidative Stress (drug effects), Peroxidase (metabolism), Phytotherapy, Plant Extracts (isolation & purification), Plant Extracts (pharmacology), Plants, Medicinal, Rats, Wistar, Trinitrobenzenesulfonic Acid.
- MESH :
- chemical , isolation & purification : Anti-Inflammatory Agents, Antioxidants, Plant Extracts.
- chemical , metabolism : Alkaline Phosphatase, Biomarkers, C-Reactive Protein, Glutathione, Inflammation Mediators, Peroxidase.
- chemical , pharmacology : Anti-Inflammatory Agents, Antioxidants, Plant Extracts.
- chemically induced : Colitis.
- chemistry : Citrus paradisi, Citrus sinensis.
- drug effects : Colon, Oxidative Stress.
- metabolism : Colitis, Colon.
- pathology : Colitis, Colon.
- prevention & control : Colitis.
- Animals, Disease Models, Animal, Dose-Response Relationship, Drug, Drug Therapy, Combination, Fruit, Fruit and Vegetable Juices, Male, Phytotherapy, Plants, Medicinal, Rats, Wistar, Trinitrobenzenesulfonic Acid.
Abstract
Citrus bioflavonoids embrace a wide group of phenolic compounds effecting the production and scavenging of reactive oxygen species and the processes relating free radical-mediated injury. Keeping in view of the antioxidant and anti-inflammatory properties of Citrus sinensis and Citrus paradisi, present study was undertaken to explore the effects of C. sinensis (orange juice) and C. paradisi (grapefruit juice) at three different doses alone and their two combinations with the objective to examine the effects of these compounds in an experimental model of rat colitis induced by trinitrobenzenesulphonic acid (TNBS). Hence biochemical parameters e.g. myeloperoxidase, alkaline phosphatase, C-reactive protein (CRP) and glutathione were assessed. Data entry and analysis was accomplished by Statistical Package for the Social Sciences version 17 and was presented as mean ± S.E.M with 95% confidence interval. Present result shows that these juices, mainly C. paradisi, may be efficacious for the management of inflammatory bowel disease. In acute colitis model, C. paradise encouraged a decrease in the extension of the lesion escorted by a decrease in the occurrence of diarrhea and reinstatement of the glutathione content. Related effects were produced by the administration of C. sinensis, which also prevented the myeloperoxidase and alkaline phosphatase actions in acute intestinal inflammatory process. The effect of the citrus juices on the inflammatory process may be associated to their antioxidant and anti-inflammatory properties, as revealed in present investigation. The favorable effects exerted were demonstrated both by histological and biochemical changes and were related with a progress in the colonic oxidative status.
PubMed: 27166529
Affiliations:
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Le document en format XML
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Karachi, Karachi, Pakistan.</nlm:affiliation><country xml:lang="fr">Pakistan</country><wicri:regionArea>Department of Pharmacology, Faculty of Pharmacy & Pharmaceutical Sciences, University of Karachi, Karachi</wicri:regionArea><wicri:noRegion>Karachi</wicri:noRegion></affiliation></author><author><name sortKey="Feroz, Zeeshan" sort="Feroz, Zeeshan" uniqKey="Feroz Z" first="Zeeshan" last="Feroz">Zeeshan Feroz</name><affiliation><nlm:affiliation>Department of Basic Sciences, College of Science and Health Profession, King Saud bin Abdulaziz University for Health Sciences, Riyadh, KSA.</nlm:affiliation><wicri:noCountry code="subField">KSA</wicri:noCountry></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2016">2016</date><idno type="RBID">pubmed:27166529</idno><idno type="pmid">27166529</idno><idno type="wicri:Area/PubMed/Corpus">000051</idno><idno type="wicri:Area/PubMed/Curation">000051</idno><idno 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Pharmacology, Faculty of Pharmacy & Pharmaceutical Sciences, University of Karachi, Karachi</wicri:regionArea><wicri:noRegion>Karachi</wicri:noRegion></affiliation></author><author><name sortKey="Mallick, Neelam" sort="Mallick, Neelam" uniqKey="Mallick N" first="Neelam" last="Mallick">Neelam Mallick</name><affiliation wicri:level="1"><nlm:affiliation>Department of Pharmacology, Faculty of Pharmacy & Pharmaceutical Sciences, University of Karachi, Karachi, Pakistan.</nlm:affiliation><country xml:lang="fr">Pakistan</country><wicri:regionArea>Department of Pharmacology, Faculty of Pharmacy & Pharmaceutical Sciences, University of Karachi, Karachi</wicri:regionArea><wicri:noRegion>Karachi</wicri:noRegion></affiliation></author><author><name sortKey="Feroz, Zeeshan" sort="Feroz, Zeeshan" uniqKey="Feroz Z" first="Zeeshan" last="Feroz">Zeeshan Feroz</name><affiliation><nlm:affiliation>Department of Basic Sciences, College of Science and Health Profession, King Saud bin Abdulaziz University for Health Sciences, Riyadh, KSA.</nlm:affiliation><wicri:noCountry code="subField">KSA</wicri:noCountry></affiliation></author></analytic><series><title level="j">Pakistan journal of pharmaceutical sciences</title><idno type="ISSN">1011-601X</idno><imprint><date when="2016" type="published">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alkaline Phosphatase (metabolism)</term><term>Animals</term><term>Anti-Inflammatory Agents (isolation & purification)</term><term>Anti-Inflammatory Agents (pharmacology)</term><term>Antioxidants (isolation & purification)</term><term>Antioxidants (pharmacology)</term><term>Biomarkers (metabolism)</term><term>C-Reactive Protein (metabolism)</term><term>Citrus paradisi (chemistry)</term><term>Citrus sinensis (chemistry)</term><term>Colitis (chemically induced)</term><term>Colitis (metabolism)</term><term>Colitis (pathology)</term><term>Colitis (prevention & control)</term><term>Colon (drug effects)</term><term>Colon (metabolism)</term><term>Colon (pathology)</term><term>Disease Models, Animal</term><term>Dose-Response Relationship, Drug</term><term>Drug Therapy, Combination</term><term>Fruit</term><term>Fruit and Vegetable Juices</term><term>Glutathione (metabolism)</term><term>Inflammation Mediators (metabolism)</term><term>Male</term><term>Oxidative Stress (drug effects)</term><term>Peroxidase (metabolism)</term><term>Phytotherapy</term><term>Plant Extracts (isolation & purification)</term><term>Plant Extracts (pharmacology)</term><term>Plants, Medicinal</term><term>Rats, Wistar</term><term>Trinitrobenzenesulfonic Acid</term></keywords><keywords scheme="MESH" type="chemical" qualifier="isolation & purification" xml:lang="en"><term>Anti-Inflammatory Agents</term><term>Antioxidants</term><term>Plant Extracts</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Alkaline Phosphatase</term><term>Biomarkers</term><term>C-Reactive Protein</term><term>Glutathione</term><term>Inflammation Mediators</term><term>Peroxidase</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Anti-Inflammatory Agents</term><term>Antioxidants</term><term>Plant Extracts</term></keywords><keywords scheme="MESH" qualifier="chemically induced" xml:lang="en"><term>Colitis</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Citrus paradisi</term><term>Citrus sinensis</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Colon</term><term>Oxidative Stress</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Colitis</term><term>Colon</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Colitis</term><term>Colon</term></keywords><keywords scheme="MESH" qualifier="prevention & control" xml:lang="en"><term>Colitis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Disease Models, Animal</term><term>Dose-Response Relationship, Drug</term><term>Drug Therapy, Combination</term><term>Fruit</term><term>Fruit and Vegetable Juices</term><term>Male</term><term>Phytotherapy</term><term>Plants, Medicinal</term><term>Rats, Wistar</term><term>Trinitrobenzenesulfonic Acid</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Citrus bioflavonoids embrace a wide group of phenolic compounds effecting the production and scavenging of reactive oxygen species and the processes relating free radical-mediated injury. Keeping in view of the antioxidant and anti-inflammatory properties of Citrus sinensis and Citrus paradisi, present study was undertaken to explore the effects of C. sinensis (orange juice) and C. paradisi (grapefruit juice) at three different doses alone and their two combinations with the objective to examine the effects of these compounds in an experimental model of rat colitis induced by trinitrobenzenesulphonic acid (TNBS). Hence biochemical parameters e.g. myeloperoxidase, alkaline phosphatase, C-reactive protein (CRP) and glutathione were assessed. Data entry and analysis was accomplished by Statistical Package for the Social Sciences version 17 and was presented as mean ± S.E.M with 95% confidence interval. Present result shows that these juices, mainly C. paradisi, may be efficacious for the management of inflammatory bowel disease. In acute colitis model, C. paradise encouraged a decrease in the extension of the lesion escorted by a decrease in the occurrence of diarrhea and reinstatement of the glutathione content. Related effects were produced by the administration of C. sinensis, which also prevented the myeloperoxidase and alkaline phosphatase actions in acute intestinal inflammatory process. The effect of the citrus juices on the inflammatory process may be associated to their antioxidant and anti-inflammatory properties, as revealed in present investigation. The favorable effects exerted were demonstrated both by histological and biochemical changes and were related with a progress in the colonic oxidative status.</div></front></TEI><affiliations><list><country><li>Pakistan</li></country></list><tree><noCountry><name sortKey="Feroz, Zeeshan" sort="Feroz, Zeeshan" uniqKey="Feroz Z" first="Zeeshan" last="Feroz">Zeeshan Feroz</name></noCountry><country name="Pakistan"><noRegion><name sortKey="Khan, Rafeeq Alam" sort="Khan, Rafeeq Alam" uniqKey="Khan R" first="Rafeeq Alam" last="Khan">Rafeeq Alam Khan</name></noRegion><name sortKey="Mallick, Neelam" sort="Mallick, Neelam" uniqKey="Mallick N" first="Neelam" last="Mallick">Neelam Mallick</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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