4.7 Article

Perinatal exposure to a glyphosate-based herbicide causes dysregulation of dynorphins and an increase of neural precursor cells in the brain of adult male rats

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TOXICOLOGY
卷 461, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.tox.2021.152922

关键词

Glyphosate-based herbicide; MALDI IMS; Substantia nigra; Hippocampus; Dynorphin; Nestin

资金

  1. Brazilian mobility program, Science Without Borders - Brazilian National Research Council (CNPq)
  2. Coordination for the Improvement of Higher Education Personnel (CAPES)
  3. Faculty of Pharmacy, Department of Pharmaceutical Biosciences, Uppsala University
  4. Swedish Research Council [2011-4423, 2015-4870]

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Using MALDI IMS, this study examined persistent changes in peptide expression in the substantia nigra (SN) of adult male Wistar rats following perinatal exposure to glyphosate-based herbicide (GBH), revealing significant alterations in peptidergic signaling in the SN. The findings suggest that perinatal GBH exposure may perturb critical neurodevelopmental processes, leading to long-term changes in the SN and hippocampus.
Glyphosate, the most used herbicide worldwide, has been suggested to induce neurotoxicity and behavioral changes in rats after developmental exposure. Studies of human glyphosate intoxication have reported adverse effects on the nervous system, particularly in substantia nigra (SN). Here we used matrix-assisted laser desorption ionization (MALDI) imaging mass spectrometry (IMS) to study persistent changes in peptide expression in the SN of 90-day-old adult male Wistar rats. The animals were perinatally exposed to 3 % GBH (glyphosate-based herbicide) in drinking water (corresponding to 0.36 % of glyphosate) starting at gestational day 5 and continued up to postnatal day 15 (PND15). Peptides are present in the central nervous system before birth and play a critical role in the development and survival of neurons, therefore, observed neuropeptide changes could provide better understanding of the GBH-induced long term effects on SN. The results revealed 188 significantly altered mass peaks in SN of animals perinatally exposed to GBH. A significant reduction of the peak intensity (P < 0.05) of several peptides from the opioid-related dynorphin family such as dynorphin B (57 %), alpha-neoendorphin (50 %), and its endogenous metabolite des-tyrosine alpha-neoendorphin (39 %) was detected in the GBH group. Immunohistochemical analysis confirmed a decreased dynorphin expression and showed a reduction of the total area of dynorphin immunoreactive fibers in the SN of the GBH group. In addition, a small reduction of dynorphin immunoreactivity associated with non-neuronal cells was seen in the hilus of the hippocampal dentate gyrus. Perinatal exposure to GBH also induced an increase in the number of nestin-positive cells in the subgranular zone of the dentate gyrus. In conclusion, the results demonstrate long-term changes in the adult male rat SN and hippocampus following a perinatal GBH exposure suggesting that this glyphosate-based formulation may perturb critical neurodevelopmental processes.

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