Melatonin enhanced the heavy metal-stress tolerance of pepper by mitigating the oxidative damage and reducing the heavy metal accumulation.
Melatonin
/ pharmacology
Cadmium
/ toxicity
Hydrogen Peroxide
/ metabolism
Antioxidants
/ metabolism
Oxidative Stress
Metals, Heavy
/ toxicity
Superoxide Dismutase
/ metabolism
Chromium
/ metabolism
Glutathione Reductase
/ metabolism
Chlorophyll
/ metabolism
Glutathione
/ metabolism
Seedlings
/ metabolism
Heavy metals
Melatonin
Oxidative stress
Photosynthetic pigments
Root growth
Journal
Journal of hazardous materials
ISSN: 1873-3336
Titre abrégé: J Hazard Mater
Pays: Netherlands
ID NLM: 9422688
Informations de publication
Date de publication:
15 07 2023
15 07 2023
Historique:
received:
12
01
2023
revised:
06
04
2023
accepted:
20
04
2023
medline:
19
5
2023
pubmed:
5
5
2023
entrez:
5
5
2023
Statut:
ppublish
Résumé
Heavy metals (HMs), like vanadium (V), chromium (Cr), cadmium (Cd), and nickel (Ni) toxicity due to anthropogenic, impair plant growth and yield, which is a challenging issue for agricultural production. Melatonin (ME) is a stress mitigating molecule, which alleviates HM-induced phytotoxicity, but the possible underlying mechanism of ME functions under HMs' phytotoxicity is still unclear. Current study uncovered key mechanisms for ME-mediated HMs-stress tolerance in pepper. HMs toxicity greatly reduced growth by impeding leaf photosynthesis, root architecture system, and nutrient uptake. Conversely, ME supplementation markedly enhanced growth attributes, mineral nutrient uptake, photosynthetic efficiency, as measured by chlorophyll content, gas exchange elements, chlorophyll photosynthesis genes' upregulation, and reduced HMs accumulation. ME treatment showed a significant decline in the leaf/root V, Cr, Ni, and Cd concentration which was about 38.1/33.2%, 38.5/25.9%, 34.8/24.9%, and 26.6/25.1%, respectively, when compared with respective HM treatment. Furthermore, ME remarkably reduced the ROS (reactive oxygen species) accumulation, and reinstated the integrity of cellular membrane via activating antioxidant enzymes (SOD, superoxide dismutase; CAT, catalase; APX, ascorbate peroxidase; GR, glutathione reductase; POD, peroxidase; GST, glutathione S-transferase; DHAR, dehydroascorbate reductase; MDHAR, monodehydroascorbate reductase) and as well as regulating ascorbate-glutathione (AsA-GSH) cycle. Importantly, oxidative damage showed efficient alleviations through upregulating the genes related to key defense such as SOD, CAT, POD, GR, GST, APX, GPX, DHAR, and MDHAR; along with the genes related to ME biosynthesis. ME supplementation also enhanced the level of proline and secondary metabolites, and their encoding genes expression, which may control excessive H
Identifiants
pubmed: 37146338
pii: S0304-3894(23)00751-3
doi: 10.1016/j.jhazmat.2023.131468
pii:
doi:
Substances chimiques
Melatonin
JL5DK93RCL
Cadmium
00BH33GNGH
Hydrogen Peroxide
BBX060AN9V
Antioxidants
0
Metals, Heavy
0
Superoxide Dismutase
EC 1.15.1.1
Chromium
0R0008Q3JB
Glutathione Reductase
EC 1.8.1.7
Chlorophyll
1406-65-1
Glutathione
GAN16C9B8O
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
131468Informations de copyright
Copyright © 2023. Published by Elsevier B.V.
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.