Corrective role of endophytic exopolysaccharides from Clerodendrum infortunatum L. on arsenic-induced ovarian steroidogenic dysfunction and associated inflammatory responses.

Androgen receptor Arsenic Endophytes Exopolysaccharides Inflammation Oxidative stress

Journal

International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578

Informations de publication

Date de publication:
21 Oct 2024
Historique:
received: 11 06 2024
revised: 09 10 2024
accepted: 20 10 2024
medline: 24 10 2024
pubmed: 24 10 2024
entrez: 23 10 2024
Statut: aheadofprint

Résumé

The present investigation aimed to evaluate the therapeutic potential of exopolysaccharides (EPSs) derived from endophytic fungi against arsenic [As(III)]-mediated metabolic and reproductive ailments. Two endophytic fungi, Diaporthe arengae (CleR1) and Fusarium proliferatum (CleR3), were isolated from Clerodendrum infortunatum (Cle), and used for the extraction of two types of EPSs. GC-MS analysis confirmed the presence of hydroxymethyl furfural (HMF) and α-d-glucopyranose in the EPS1 (CleR1) and EPS2 (CleR3), respectively. FTIR analysis revealed the potential As(III)-chelation properties of both EPSs. EPS1 and EPS2 significantly mitigated As(III)-induced oxidative stress and lipid peroxidation by restoring the activities of antioxidative enzymes. EPSs successfully corrected the gonadotropin imbalance and steroidogenic alterations. The downregulation of proinflammatory (NF-κB and TNF-α) and proapoptotic (BAX) mediators and the upregulation of antiapoptotic (Bcl2) markers were also detected following the treatment with EPSs. Histomorphological restoration of reproductive and metabolic organs was also observed in both the EPS groups. Moreover, the As(III)-induced increase in the immunoreactivity of the androgen receptor (AR) was successfully reversed by these EPSs. Molecular docking predicted that HMF and α-d-glucopyranose of EPS1 and EPS2 interact with the active site of AR by limiting its activity. Hence, EPS could be effective for developing new therapeutic strategies for managing As(III) toxicity.

Identifiants

pubmed: 39442839
pii: S0141-8130(24)07604-9
doi: 10.1016/j.ijbiomac.2024.136795
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

136795

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

Sangita Saha (S)

Centre for Life Sciences, Vidyasagar University, Midnapore 721102, West Bengal, India; Cellular and Molecular Toxicology Laboratory, Department of Biomedical Laboratory Science and Management, Vidyasagar University, Midnapore 721102, West Bengal, India; Microbiology and Microbial Biotechnology Laboratory, Department of Botany and Forestry, Vidyasagar University, Midnapore 721102, West Bengal, India.

Angshita Ghosh (A)

Cellular and Molecular Toxicology Laboratory, Department of Biomedical Laboratory Science and Management, Vidyasagar University, Midnapore 721102, West Bengal, India.

Hiran Kanti Santra (HK)

Microbiology and Microbial Biotechnology Laboratory, Department of Botany and Forestry, Vidyasagar University, Midnapore 721102, West Bengal, India.

Debdulal Banerjee (D)

Centre for Life Sciences, Vidyasagar University, Midnapore 721102, West Bengal, India; Microbiology and Microbial Biotechnology Laboratory, Department of Botany and Forestry, Vidyasagar University, Midnapore 721102, West Bengal, India.

Sandip Chattopadhyay (S)

Centre for Life Sciences, Vidyasagar University, Midnapore 721102, West Bengal, India; Cellular and Molecular Toxicology Laboratory, Department of Biomedical Laboratory Science and Management, Vidyasagar University, Midnapore 721102, West Bengal, India. Electronic address: sandipdoc@yahoo.com.

Classifications MeSH