Comprehensive assessment of Zingiber sianginensis: Phytometabolomic analysis and its impact on oxidative stress biomarkers.

Active constituent isolation And characterisation Oxidative stress biomarkers Phytometabolomics Zingiber sianginensis

Journal

Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336

Informations de publication

Date de publication:
15 Aug 2024
Historique:
received: 31 05 2024
revised: 06 08 2024
accepted: 13 08 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 29 8 2024
Statut: aheadofprint

Résumé

In India, ginger is highly valued for cultural and medicinal purposes. Besides traditional uses, ginger has been proven for its efficacy in cancer, chemotherapy-induced nausea, bacterial infections, neuroinflammation, and oxidative stress. This study focuses on Zingiber sianginensis, a rare ginger species in the Siang region of Arunachal Pradesh, India. This study studied pharmacognostical evaluation, phytometabolomics analysis, and its effect on oxidative stress biomarkers. Microscopic and chemical tests were employed for pharmacognostical evaluation, revealing distinctive characteristics of Zingiber sianginensis, such as non-close collateral vascular bundles and unique cork layers. Chemical tests, including the phloroglucinol and hydrochloric acid test, differentiated Zingiber sianginensis from Zingiber officinale Roscoe. Phytometabolomics analysis, using Gas Chromatography-Mass Spectrometry (GC/MS) and Liquid Chromatography-Electrospray Ionisation-Quadrupole Time of Flight-Mass Spectrometry (LC-ESI-QTOF-MS/MS) techniques, identified a diverse range of metabolites in Zingiber sianginensis, including polyphenols, monoterpenoids, diterpenoids, sesquiterpenoids, and organic compounds. The LC-ESI-QTOF-MS/MS analysis revealed 158 compounds, verified through cross-referencing with established databases. Heavy metal analysis by Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) confirmed that Zingiber sianginensis complies with safety standards, showing concentrations of heavy metals within acceptable limits. The isolation and characterization of compounds from Zingiber sianginensis identified natural products such as (R)-(-)- alpha-Curcumene (1), 1-Dehydro-[10]-gingerdione (2), 6-Shogaol (3), and 6-Gingerol (4). Quantification of 6-gingerol revealed that Zingiber sianginensis contains approximately twice the amount compared to Zingiber officinale Roscoe's, suggesting its potential as a source for higher 6-gingerol content. The hydroalcoholic extract of Zingiber sianginensis exhibited antioxidant properties, reducing oxidative stress biomarkers in human dermal fibroblast cells treated with rotenone. Allantoin and 3-bromotyrosine levels significantly decreased, indicating the extract's potential in combating oxidative stress-related disorders. Overall, this comprehensive study provides valuable insights into the pharmacognostical, phytometabolomic, and safety aspects of Zingiber sianginensis, highlighting its potential as a source of bioactive compounds with health benefits.

Identifiants

pubmed: 39208650
pii: S0731-7085(24)00461-8
doi: 10.1016/j.jpba.2024.116421
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

116421

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Rahul G Moriya (RG)

Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India.

A Parthiban (A)

Centre for GMP extraction Facility, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India.

Nayanika Devi (N)

Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India.

Sachin B Jorvekar (SB)

Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India.

Rupam Sankar Baruah (RS)

Assam Bio-Resource Centre, Assam Science Technology and Environment Council, Baihata Chariali, Guwahati 781381, India.

Bidisha Biswas (B)

Department of Biotechnology, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India.

Nilotpal Saharia (N)

Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India.

Srinivas Rao (S)

Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India.

Jagdish S Bankar (JS)

Department of Pharmaceutical Sciences, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur 440033, India.

Satyendra K Prasad (SK)

Department of Pharmaceutical Sciences, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur 440033, India.

S Sudhagar (S)

Department of Biotechnology, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India.

Upadhyayula Suryanarayana Murty (US)

Centre for GMP extraction Facility, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India.

Roshan M Borkar (RM)

Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India; Centre for GMP extraction Facility, National Institute of Pharmaceutical Education and Research, Changsari, Guwahati 781101, India. Electronic address: roshanudps@gmail.com.

Classifications MeSH