Monocrotaline induces acutely cerebrovascular lesions, astrogliosis and neuronal degeneration associated with behavior changes in rats : A model of vascular damage in perspective
Copyright © 2022 Elsevier B.V. All rights reserved..
Pyrrolizidine alkaloids (PAs) are secondary plant metabolites playing an important role as phytotoxins in the plant defense mechanisms and can be present as contaminant in the food of humans and animals. The PA monocrotaline (MCT), one of the major plant derived toxin that affect humans and animals, is present in a high concentration in Crotalaria spp. (Leguminosae) seeds and can induce toxicity after consumption, characterized mainly by hepatotoxicity and pneumotoxicity. However, the effects of the ingestion of MCT in the central nervous system (CNS) are still poorly elucidated. Here we investigated the effects of MCT oral acute administration on the behavior and CNS toxicity in rats. Male adult Wistar were treated with MCT (109 mg/Kg, oral gavage) and three days later the Elevated Pluz Maze test demonstrated that MCT induced an anxiolytic-like effect, without changes in novelty habituation and in operational and spatial memory profiles. Histopathology revealed that the brain of MCT-intoxicated animals presented hyperemic vascular structures in the hippocampus, parahippocampal cortex and neocortex, mild perivascular edema in the neocortex, hemorrhagic focal area in the brain stem, hemorrhage and edema in the thalamus. MCT also induced neurotoxicity in the cortex and hippocampus, as revealed by Fluoro Jade-B and Cresyl Violet staining, as well astrocyte reactivity, revealed by immunocytochemistry for glial fibrillary acidic protein. Additionally, it was demonstrated by RT-qPCR that MCT induced up-regulation on mRNA expression of neuroinflammatory mediator, especially IL1β and CCL2 in the hippocampus and cortex, and down-regulation on mRNA expression of neurotrophins HGDF and BDNF in the cortex. Together, these results demonstrate that the ingestion of MCT induces cerebrovascular lesions and toxicity to neurons that are associated to astroglial cell response and neuroinflammation in the cortex and hippocampus of rats, highlighting CNS damages after acute intoxication, also putting in perspective it uses as a model for cerebrovascular damage.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2023 |
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| Erschienen: |
2023 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:94 |
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| Enthalten in: |
Neurotoxicology - 94(2023) vom: 01. Jan., Seite 59-70 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Silva, Adriana L [VerfasserIn] |
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| Links: |
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| Themen: |
73077K8HYV |
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| Anmerkungen: |
Date Completed 11.01.2023 Date Revised 05.02.2023 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1016/j.neuro.2022.10.017 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| 100 | 1 | |a Silva, Adriana L |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Monocrotaline induces acutely cerebrovascular lesions, astrogliosis and neuronal degeneration associated with behavior changes in rats |b A model of vascular damage in perspective |
| 264 | 1 | |c 2023 | |
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| 500 | |a Date Revised 05.02.2023 | ||
| 500 | |a published: Print-Electronic | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a Copyright © 2022 Elsevier B.V. All rights reserved. | ||
| 520 | |a Pyrrolizidine alkaloids (PAs) are secondary plant metabolites playing an important role as phytotoxins in the plant defense mechanisms and can be present as contaminant in the food of humans and animals. The PA monocrotaline (MCT), one of the major plant derived toxin that affect humans and animals, is present in a high concentration in Crotalaria spp. (Leguminosae) seeds and can induce toxicity after consumption, characterized mainly by hepatotoxicity and pneumotoxicity. However, the effects of the ingestion of MCT in the central nervous system (CNS) are still poorly elucidated. Here we investigated the effects of MCT oral acute administration on the behavior and CNS toxicity in rats. Male adult Wistar were treated with MCT (109 mg/Kg, oral gavage) and three days later the Elevated Pluz Maze test demonstrated that MCT induced an anxiolytic-like effect, without changes in novelty habituation and in operational and spatial memory profiles. Histopathology revealed that the brain of MCT-intoxicated animals presented hyperemic vascular structures in the hippocampus, parahippocampal cortex and neocortex, mild perivascular edema in the neocortex, hemorrhagic focal area in the brain stem, hemorrhage and edema in the thalamus. MCT also induced neurotoxicity in the cortex and hippocampus, as revealed by Fluoro Jade-B and Cresyl Violet staining, as well astrocyte reactivity, revealed by immunocytochemistry for glial fibrillary acidic protein. Additionally, it was demonstrated by RT-qPCR that MCT induced up-regulation on mRNA expression of neuroinflammatory mediator, especially IL1β and CCL2 in the hippocampus and cortex, and down-regulation on mRNA expression of neurotrophins HGDF and BDNF in the cortex. Together, these results demonstrate that the ingestion of MCT induces cerebrovascular lesions and toxicity to neurons that are associated to astroglial cell response and neuroinflammation in the cortex and hippocampus of rats, highlighting CNS damages after acute intoxication, also putting in perspective it uses as a model for cerebrovascular damage | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Research Support, Non-U.S. Gov't | |
| 650 | 4 | |a Astrogliosis | |
| 650 | 4 | |a Behavioral changes | |
| 650 | 4 | |a Monocrotaline | |
| 650 | 4 | |a Oral intoxication, cerebrovascular disorders | |
| 650 | 7 | |a Monocrotaline |2 NLM | |
| 650 | 7 | |a 73077K8HYV |2 NLM | |
| 650 | 7 | |a RNA, Messenger |2 NLM | |
| 700 | 1 | |a Oliveira, Joana L |e verfasserin |4 aut | |
| 700 | 1 | |a do Nascimento, Ravena P |e verfasserin |4 aut | |
| 700 | 1 | |a Santos, Letícia O |e verfasserin |4 aut | |
| 700 | 1 | |a de Araújo, Fillipe M |e verfasserin |4 aut | |
| 700 | 1 | |a Dos Santos, Balbino L |e verfasserin |4 aut | |
| 700 | 1 | |a Santana, Rejane C |e verfasserin |4 aut | |
| 700 | 1 | |a Moreira, Eduardo Luiz T |e verfasserin |4 aut | |
| 700 | 1 | |a Batatinha, Maria José M |e verfasserin |4 aut | |
| 700 | 1 | |a Alves, Iura M |e verfasserin |4 aut | |
| 700 | 1 | |a Velozo, Eudes S |e verfasserin |4 aut | |
| 700 | 1 | |a Victor, Mauricio M |e verfasserin |4 aut | |
| 700 | 1 | |a Assis, Adriano M |e verfasserin |4 aut | |
| 700 | 1 | |a Almeida, Roberto F |e verfasserin |4 aut | |
| 700 | 1 | |a de Souza, Diogo O G |e verfasserin |4 aut | |
| 700 | 1 | |a Silva, Victor Diógenes A |e verfasserin |4 aut | |
| 700 | 1 | |a Costa, Silvia L |e verfasserin |4 aut | |
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