Journal

Current pharmaceutical biotechnology
ISSN: 1873-4316
Titre abrégé: Curr Pharm Biotechnol
Pays: Netherlands
ID NLM: 100960530

Informations de publication

Date de publication:
2022
Historique:
received: 21 09 2020
revised: 19 01 2021
accepted: 13 04 2021
pubmed: 7 7 2021
medline: 12 2 2022
entrez: 6 7 2021
Statut: ppublish

Résumé

Raphanus sativus is traditionally used as an anti-inflammatory agent. The current study was designed to explore the in vivo anti-inflammatory and antiangiogenic properties of Raphanus sativus seeds oil. Cold press method was used for the extraction of oil (RsSO) and was characterised by using GC-MS techniques. Three in vitro antioxidant assays (DPPH, ABTS and FRAP) were performed to explore the antioxidant potential of RsSO. Disc diffusion methods were used to study in vitro antimicrobial properties. In vivo anti-inflammatory properties were studied in both acute and chronic inflammation models. In vivo chicken chorioallantoic membrane assay was performed to study antiangiogenic effects. Molecular mechanisms were identified using TNF-α ELISA kit and docking tools. GC-MS analysis of RsSO revealed the presence of hexadecanoic and octadecanoic acid. Findings of DPPH, ABTS, and FRAP models indicated relatively moderate radical scavenging properties of RsSO. Oil showed antimicrobial activity against a variety of bacterial and fungal strains tested. Data of inflammation models showed significant (p < 0.05) anti-inflammatory effects of RsSO in both acute and chronic models. 500 mg/kg RsSO halted inflammation development significantly better (p < 0.05) as compared with lower doses. Histopathological evaluations of paws showed minimal infiltration of inflammatory cells in RsSO-treated animals. Findings of TNF-α ELSIA and docking studies showed that RsSO has the potential to down-regulate the expression of TNF-α, iNOS, ROS, and NF-κB respectively. Moreover, RsSO showed in vivo antiangiogenic effects. Data of the current study highlight that Raphanus sativus seeds oil has anti-inflammatory, and antiangiogenic properties and can be used as an adjunct to standard NSAIDs therapy which may reduce the dose and related side effects.

Sections du résumé

BACKGROUND BACKGROUND
Raphanus sativus is traditionally used as an anti-inflammatory agent.
OBJECTIVES OBJECTIVE
The current study was designed to explore the in vivo anti-inflammatory and antiangiogenic properties of Raphanus sativus seeds oil.
METHODS METHODS
Cold press method was used for the extraction of oil (RsSO) and was characterised by using GC-MS techniques. Three in vitro antioxidant assays (DPPH, ABTS and FRAP) were performed to explore the antioxidant potential of RsSO. Disc diffusion methods were used to study in vitro antimicrobial properties. In vivo anti-inflammatory properties were studied in both acute and chronic inflammation models. In vivo chicken chorioallantoic membrane assay was performed to study antiangiogenic effects. Molecular mechanisms were identified using TNF-α ELISA kit and docking tools.
RESULTS RESULTS
GC-MS analysis of RsSO revealed the presence of hexadecanoic and octadecanoic acid. Findings of DPPH, ABTS, and FRAP models indicated relatively moderate radical scavenging properties of RsSO. Oil showed antimicrobial activity against a variety of bacterial and fungal strains tested. Data of inflammation models showed significant (p < 0.05) anti-inflammatory effects of RsSO in both acute and chronic models. 500 mg/kg RsSO halted inflammation development significantly better (p < 0.05) as compared with lower doses. Histopathological evaluations of paws showed minimal infiltration of inflammatory cells in RsSO-treated animals. Findings of TNF-α ELSIA and docking studies showed that RsSO has the potential to down-regulate the expression of TNF-α, iNOS, ROS, and NF-κB respectively. Moreover, RsSO showed in vivo antiangiogenic effects.
CONCLUSION CONCLUSIONS
Data of the current study highlight that Raphanus sativus seeds oil has anti-inflammatory, and antiangiogenic properties and can be used as an adjunct to standard NSAIDs therapy which may reduce the dose and related side effects.

Identifiants

pubmed: 34225619
pii: CPB-EPUB-116432
doi: 10.2174/1389201022666210702120956
doi:

Substances chimiques

Plant Extracts 0
Tumor Necrosis Factor-alpha 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

728-739

Subventions

Organisme : Higher Education Commission of Pakistan
ID : 21-1828/SRGP/R&amp;D/HEC/2018

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Muhammad Asif (M)

Department of Pharmacology, Faculty of Pharmacy, The Islamia University of Bahawalpur, Punjab, Pakistan.

Hafiz Muhammad Yousaf (HM)

Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Pakistan.

Mohammad Saleem (M)

University College of Pharmacy, University of the Punjab, Lahore, Pakistan.

Liaqat Hussain (L)

Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Pakistan.
Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Pakistan.

Raghdaa Al Zarzour (RA)

Discipline of Pharmacology, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Malaysia.

Tahir Chohan (T)

Institute of Pharmaceutical Sciences, University of Veterinary and Animal Sciences, Lahore, Pakistan.

Malik Saadullah (M)

Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Pakistan.

Muhammad Usman Shamas (MU)

FMH College of Medicine and Dentistry, Lahore, Pakistan.

Hafiza Sidra Yaseen (HS)

Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Pakistan.

Muhammad Umair Yousaf (MU)

Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Pakistan.

Ikram Ullah Khan (IU)

Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Pakistan.

Muhammad Azam Tahir (MA)

Department of Pharmaceutics, Institute of Pharmacy, The University of Bonn, Bonn, Germany.

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Classifications MeSH