Comparative effects of the Roundup and glyphosate on mitochondrial oxidative phosphorylation
Abstract
The potential toxicity of the herbicide Roundup and its fundamental substance (glyphosate) was tested in bioenergetic functions of isolated rat liver mitochondria. Roundup stimulates succinate-supported respiration twice, with simultaneous collapse of transmembrane electrical potential, while glyphosate used in the same concentrations does not induce any significant effect. Additionally, Roundup depresses state 3 respiration by about 40%, at 15 mM, whereas uncoupled respiration in the presence of FCCP is depressed by about 50%. Depression of uncoupled respiratory activity is mediated through partial inhibition of mitochondrial complexes II and III, but not of complex IV. The phosphorylative system was affected by both a direct and an indirect effect on the F0F1 ATPase activity. The addition of uncoupled concentrations of Roundup to Ca2+-loaded mitochondria treated with Ruthenium Red resulted in non-specific membrane permeabilization, as evidenced by mitochondrial swelling in isosmotic sucrose medium. Therefore, the uncoupling of oxidative phosphorylation is also related to the non-specific membrane permeabilization induced by Roundup. Glyphosate alone does not show any relevant effect on the mitochondrial bioenergetics, in opposition to Roundup formulation products. The differences in the toxicity observed could be either attributed to some products of Roundup or to a synergic effect of glyphosate and formulation products. Bearing in mind that mitochondria is provided with a variety of bioenergetic functions mandatory for the regulation of intracellular aerobic energy production and electrolyte homeostasis, these results question the safety of Roundup on animal health.
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This is consistent with the well-documented toxic effect of very low dilutions of R on apoptosis, mitochondrial function, and cell membrane degradation, inducing necrosis of hepatocytes, and in other cell lines.
“This is consistent with the well-documented toxic effect of very low dilutions of R on apoptosis, mitochondrial function, and cell membrane degradation, inducing necrosis of hepatocytes, and in other cell lines [8,9,44,45].”
From Republished study: long-term toxicity of a Roundup herbicide and a Roundup-tolerantgenetically modified maize (2014) · cites this paper as [45]
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References 33 · Cited by 259
- Authors
- Peixoto, F.
- Affiliations
- University of Trás-os-Montes and Alto Douro (PT)
- Corresponding author
- Peixoto, Francisco
- ORCID
- Peixoto, Francisco
- Venue
- Chemosphere
- Publisher
- Elsevier BV
- Published
- 2005-12
- Volume
- 61
- Issue
- 8
- Pages
- 1115-1122
- ISSN
- 0045-6535 (ISSN-L)
- OpenAlex
- W2149992333
- Cited by
- 259
- References
- 33
- Citations by year
- 2026: 16 · 2025: 9 · 2024: 13 · 2023: 11 · 2022: 16 · 2021: 10 · 2020: 15 · 2019: 17 · 2018: 22 · 2017: 9 · 2016: 19 · 2015: 12 · 2014: 11 · 2013: 9 · 2012: 15
- FWCI
- 8.79
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Chemosphere (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Pesticide Exposure and Toxicity
- Physical Sciences › Environmental Science › Pollution › Pesticide and Herbicide Environmental Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Keywords
- Roundup, glyphosate, herbicide toxicity, mitochondrial oxidative phosphorylation, liver mitochondria, membrane potential, state 3 respiration, uncoupled respiration, FCCP, succinate dehydrogenase, mitochondrial complex III, ATP synthase, membrane permeabilization, mitochondrial swelling, synergistic toxicity
- MeSH terms
- Glyphosate, Adenosine Diphosphate, Adenosine Triphosphatases, Animals, Electron Transport Complex IV, Drug Synergism, Glycine, Herbicides, Membrane Potentials, Mitochondria, Liver, Mitochondrial Swelling, Oxidative Phosphorylation, Succinate Cytochrome c Oxidoreductase, Succinate Dehydrogenase, Rats, Wistar, Mitochondrial Proton-Translocating ATPases, Rats, In Vitro Techniques
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