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Oleanolic acid-3-glucoside, a synthetic oleanane-type saponin, ameliorates methylmercury-induced dysfunction of synaptic transmission in mice.
- Source :
-
Toxicology [Toxicology] 2024 Aug; Vol. 506, pp. 153867. Date of Electronic Publication: 2024 Jun 19. - Publication Year :
- 2024
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Abstract
- Methylmercury (MeHg) is widely distributed in nature and is known to cause neurotoxic effects. This study aimed to examine the anti-MeHg activity of oleanolic acid-3-glucoside (OA3Glu), a synthetic oleanane-type saponin derivative, by evaluating its effects on motor function, pathology, and electrophysiological properties in a mouse model of MeHg poisoning. Mice were orally administered 2 or 4 mg·kg <superscript>-1</superscript> ·d <superscript>-1</superscript> MeHg with or without 100 µg·kg <superscript>-1</superscript> ·d <superscript>-1</superscript> OA3Glu 5x/week for four weeks. Motor function was evaluated using beam-walking and dynamic weight-bearing (DWB) tests. High-dose MeHg exposure significantly increased the frequency of stepping off the hind leg while crossing the beam in the beam-walking test, and increased weight on forelegs when moving freely in the DWB test. OA3Glu treatment alleviated motor abnormality caused by high-dose MeHg exposure in both motor function tests. Additionally, OA3Glu treatment reduced the number of contracted Purkinje cells frequently observed in the cerebellum of MeHg-treated groups, although cerebrum histology was similar in all experimental groups. The synaptic potential amplitude in the cerebellum decreased as MeHg exposure increased, which was restored by OA3Glu treatment. Even in the cerebrum, where the effects of MeHg were not observed, the amplitude of the field potential was suppressed with increasing MeHg exposure but was restored with OA3Glu treatment. Taken together, the study findings suggest that OA3Glu improves neurotransmission and movement disorders associated with MeHg exposure via protection of Purkinje cells in the cerebellum while ameliorating pre/post-synaptic deficits in the cerebral cortex in which no changes were observed at the tissue level, potentially providing a treatment to mitigate MeHg toxicity.<br />Competing Interests: 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.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Male
Mice
Glucosides pharmacology
Purkinje Cells drug effects
Purkinje Cells pathology
Cerebellum drug effects
Cerebellum pathology
Cerebellum metabolism
Motor Activity drug effects
Mice, Inbred ICR
Methylmercury Compounds toxicity
Oleanolic Acid pharmacology
Oleanolic Acid analogs & derivatives
Synaptic Transmission drug effects
Saponins pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1879-3185
- Volume :
- 506
- Database :
- MEDLINE
- Journal :
- Toxicology
- Publication Type :
- Academic Journal
- Accession number :
- 38906242
- Full Text :
- https://doi.org/10.1016/j.tox.2024.153867