Dietary Antioxidants Significantly Reduced Phorbol Myristate Acetate Induced Oxidative Stress of Peripheral Blood Mononuclear Cells of Patients with Rheumatoid Arthritis.


Journal

Current rheumatology reviews
ISSN: 1875-6360
Titre abrégé: Curr Rheumatol Rev
Pays: United Arab Emirates
ID NLM: 101261938

Informations de publication

Date de publication:
2021
Historique:
received: 01 04 2020
revised: 24 06 2020
accepted: 29 06 2020
pubmed: 31 7 2020
medline: 25 11 2021
entrez: 31 7 2020
Statut: ppublish

Résumé

Rheumatoid arthritis (RA) is an autoimmune disease responsible for maximum human morbidity in modern life, whereas oxidative stress is the ultimate potential biomarker for determining disease activity in patients with RA. The present study scientifically validated the effectiveness of antioxidants commonly present in different food supplements to neutralize the free radicals mediated oxidative stress in isolated peripheral blood mononuclear lymphocytes (PBML) of patients with RA. The study population included patients with Rheumatoid arthritis, RA (n =15), who fulfilled the American College of Rheumatology criteria for RA. Peripheral blood was collected, and isolated mononuclear lymphocyte cells (PBML) were pretreated with phorbol myristate acetate (PMS) and furthermore, incubated with different concentrations of Naringenin, β carotene and Nacetyl cysteine (NAC) in an ex vivo condition. The resultant cell lysate was used for further studies for the determination of other oxidative biomarkers. The increase of superoxide and nitric oxide production was observed when PBML was treated PMS. Importantly, the increased oxidative stress was effectively decreased by the selected plantderived compounds β-carotene and naringenin. The study scientifically evaluated the efficacy of the molecules validated by one-way ANOVA, followed by Dunnett's post hoc test of significance. Collectively, our results indicate that both β carotene and naringenin may be a promising non-toxic food supplement in attenuating the oxidative stress associated pathology in RA, meriting further pharmacological studies on other inflammatory cells like neutrophils.

Sections du résumé

BACKGROUND BACKGROUND
Rheumatoid arthritis (RA) is an autoimmune disease responsible for maximum human morbidity in modern life, whereas oxidative stress is the ultimate potential biomarker for determining disease activity in patients with RA.
OBJECTIVE OBJECTIVE
The present study scientifically validated the effectiveness of antioxidants commonly present in different food supplements to neutralize the free radicals mediated oxidative stress in isolated peripheral blood mononuclear lymphocytes (PBML) of patients with RA.
METHODS METHODS
The study population included patients with Rheumatoid arthritis, RA (n =15), who fulfilled the American College of Rheumatology criteria for RA. Peripheral blood was collected, and isolated mononuclear lymphocyte cells (PBML) were pretreated with phorbol myristate acetate (PMS) and furthermore, incubated with different concentrations of Naringenin, β carotene and Nacetyl cysteine (NAC) in an ex vivo condition. The resultant cell lysate was used for further studies for the determination of other oxidative biomarkers. The increase of superoxide and nitric oxide production was observed when PBML was treated PMS.
RESULTS RESULTS
Importantly, the increased oxidative stress was effectively decreased by the selected plantderived compounds β-carotene and naringenin.
CONCLUSION CONCLUSIONS
The study scientifically evaluated the efficacy of the molecules validated by one-way ANOVA, followed by Dunnett's post hoc test of significance. Collectively, our results indicate that both β carotene and naringenin may be a promising non-toxic food supplement in attenuating the oxidative stress associated pathology in RA, meriting further pharmacological studies on other inflammatory cells like neutrophils.

Identifiants

pubmed: 32729420
pii: CRR-EPUB-108662
doi: 10.2174/1573397116999200729154954
doi:

Substances chimiques

Antioxidants 0
Tetradecanoylphorbol Acetate NI40JAQ945

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

81-87

Informations de copyright

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

Auteurs

Purbajit Chetia (P)

Department of Pharmacology, Himalayan Pharmacy Institute, Majhitar, Rangpo, East Sikkim 737136, Sikkim, India.

Bidita Khandelwal (B)

Department of Medicine, Sikkim Manipal Institute of Medical Science, 5th Mile Tadong, Gangtok 737102, Sikkim, India.

Pallab Kanti Haldar (PK)

Department of Pharmaceutical Technology, Jadavpur University, 188B Raja SC Mullick Road, Kolkata 700032, West Bengal, India.

Asis Bala (A)

Division of Pharmacology, Guru Nanak Institute of Pharmaceutical Science and Technology, Sodepur, Pin- 700114, West Bengal, India.

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Classifications MeSH