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Beta-Boswellic Acid Reverses 3-Nitropropionic Acid-Induced Molecular, Mitochondrial, and Histopathological Defects in Experimental Rat Model of Huntington’s Disease
Huntington’s disease (HD) is distinguished by a triple repeat of CAG in exon 1, an increase in poly Q in the Htt gene, and a loss of GABAergic medium spiny neurons (MSN) in the striatum and white matter of the cortex. Mitochondrial ETC-complex dysfunctions are involved in the pathogenesis of HD, inc...
Autores principales: | Albekairi, Thamer H., Kamra, Arzoo, Bhardwaj, Sudeep, Mehan, Sidharth, Giri, Aditi, Suri, Manisha, Alshammari, Abdulrahman, Alharbi, Metab, Alasmari, Abdullah F., Narula, Acharan S, Kalfin, Reni |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687177/ https://www.ncbi.nlm.nih.gov/pubmed/36359390 http://dx.doi.org/10.3390/biomedicines10112866 |
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