Inhibition of cartilage degeneration and subchondral bone deterioration by


Journal

Food & function
ISSN: 2042-650X
Titre abrégé: Food Funct
Pays: England
ID NLM: 101549033

Informations de publication

Date de publication:
23 Sep 2020
Historique:
pubmed: 10 9 2020
medline: 23 7 2021
entrez: 9 9 2020
Statut: ppublish

Résumé

Osteoarthritis (OA) is an aging disorder characterized by degenerated cartilage and sub-chondral bone alteration in affected knee joints. Globally, millions of people suffer from this disease. However, there is a lack of safe and promising therapeutics, making the exploration and development of leads from natural sources urgent. Accordingly, food as medicine may be the most suitable approach for the treatment of this degenerative disease. Herein, we elucidated the protective role of Spinacia oleracea extract (SOE) in an anterior cruciate ligament transection (ACLT) model of osteoarthritis as a mimic of the human condition. ACL transection was done in the tibio-femoral joints of rats. SOE was orally administered at the dosage of 125 and 250 mg kg-1 day-1 for four weeks. It was shown that the animals with SOE treatment had better joint morphology than the ACLT animals, as evident by the shiny appearance of their cartilage. Hematoxylin and safranin-o staining showed that the number of chondrocytes was significantly reduced in the OA model, which was prevented with SOE treatment. The reduction in the cartilage thickness was well observed by toluidine blue staining. The reduced stain by safranin-o and toluidine blue, indicated proteoglycan loss in the ACLT-induced osteoarthritis model. The proteoglycan content and cartilage thickness were restored in the SOE group upon treatment at an SOE dosage of 125 and 250 mg kg-1 day-1. The micro-CT parameters of subchondral bone (SCB) and cartilage degradation markers in the serum corroborated our findings of the protective effects of SOE. In summary, our study suggests that SOE has therapeutic potential, which if taken regularly as a food supplement, can have beneficial effects.

Identifiants

pubmed: 32901645
doi: 10.1039/d0fo01125h
doi:

Substances chimiques

Plant Extracts 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8273-8285

Auteurs

Priyanka Kothari (P)

Endocrinology Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India. ritu_trivedi@cdri.res.in.

Shradha Sinha (S)

Endocrinology Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India. ritu_trivedi@cdri.res.in and Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.

Anirban Sardar (A)

Endocrinology Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India. ritu_trivedi@cdri.res.in and Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.

Ashish Kumar Tripathi (AK)

Endocrinology Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India. ritu_trivedi@cdri.res.in.

Aboli Girme (A)

Pharmanza Herbal Pvt Ltd, Anand, Gujarat 388435, India.

Sulekha Adhikary (S)

Endocrinology Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India. ritu_trivedi@cdri.res.in.

Ruchi Singh (R)

Pharmanza Herbal Pvt Ltd, Anand, Gujarat 388435, India.

Rakesh Maurya (R)

Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India.

Prabhat Ranjan Mishra (PR)

Pharmaceutics & Pharmacokinetics Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India.

Lal Hingorani (L)

Pharmanza Herbal Pvt Ltd, Anand, Gujarat 388435, India.

Ritu Trivedi (R)

Endocrinology Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India. ritu_trivedi@cdri.res.in and Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.

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