Protective role of diosmin against testosterone propionate-induced prostatic hyperplasia in Wistar rats: Plausible role of oxidative stress and inflammation.


Journal

Human & experimental toxicology
ISSN: 1477-0903
Titre abrégé: Hum Exp Toxicol
Pays: England
ID NLM: 9004560

Informations de publication

Date de publication:
Sep 2020
Historique:
pubmed: 5 12 2019
medline: 17 3 2021
entrez: 5 12 2019
Statut: ppublish

Résumé

Benign prostatic hyperplasia (BPH) is an important key health concern for aging men. Polyphenolic compounds have been found to possess important roles in the inhibition of numerous ailments that involve reactive oxygen species and inflammation. Diosmin is a citrus flavone that possesses antioxidant, anti-inflammatory, antiproliferative, and anticancer activities, so based on these properties of diosmin, we decided to evaluate its effect on testosterone propionate (TP)-induced BPH. A total of 30 Wistar rats were randomly assigned to five groups having six animals in each. This study was of 28 days in which TP (5 mg kg

Identifiants

pubmed: 31797688
doi: 10.1177/0960327119889655
doi:

Substances chimiques

Anti-Inflammatory Agents, Non-Steroidal 0
Antineoplastic Agents 0
Diosmin 7QM776WJ5N
Catalase EC 1.11.1.6
Glutathione Peroxidase EC 1.11.1.9
Glutathione Reductase EC 1.8.1.7
Prostate-Specific Antigen EC 3.4.21.77
Glutathione GAN16C9B8O
Testosterone Propionate WI93Z9138A

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1133-1146

Auteurs

A Vafa (A)

Section of Molecular Carcinogenesis and Chemoprevention, Department of Medical Elementology and Toxicology, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi, India.

S M Afzal (SM)

Section of Molecular Carcinogenesis and Chemoprevention, Department of Medical Elementology and Toxicology, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi, India.

P Barnwal (P)

Section of Molecular Carcinogenesis and Chemoprevention, Department of Medical Elementology and Toxicology, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi, India.

S Rashid (S)

Section of Molecular Carcinogenesis and Chemoprevention, Department of Medical Elementology and Toxicology, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi, India.
Department of Pharmacology and Toxicology, College of Pharmacy, Girls Section, Prince Sattam Bin Abdulaziz University, Al-Kharj, KSA.

A Shahid (A)

Section of Molecular Carcinogenesis and Chemoprevention, Department of Medical Elementology and Toxicology, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi, India.
Section of Molecular Carcinogenesis and Chemoprevention, Department of Medical Elementology and Toxicology, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi, India.

J Islam (J)

Section of Molecular Carcinogenesis and Chemoprevention, Department of Medical Elementology and Toxicology, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi, India.

S Sultana (S)

Section of Molecular Carcinogenesis and Chemoprevention, Department of Medical Elementology and Toxicology, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi, India.

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Classifications MeSH