Paper Details 
Original Abstract of the Article :
In this study, we were aimed to investigate the neuroprotective effects of bexarotene and nicotinamide in synaptosomes incubated with amyloid-beta (Aβ). Our study consists of 2 parts, in vivo and in vitro. In the in vivo section, twenty-four Wistar albino male rats were divided into 4 groups (contro...See full text at original site
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引用元:
https://doi.org/10.1007/s11064-020-03216-7

データ提供:米国国立医学図書館(NLM)

Bexarotene and Nicotinamide: Neuroprotective Agents Against Aβ(1-42)

This study examines the neuroprotective effects of bexarotene and nicotinamide against amyloid-beta (Aβ) toxicity in rat synaptosomes. The researchers conducted both in vivo and in vitro studies to assess the impact of these agents on oxidative stress and apoptosis in synaptosomes treated with Aβ(1-42).

Exploring the Neuroprotective Potential of Bexarotene and Nicotinamide

The study found that both bexarotene and nicotinamide provided neuroprotection against Aβ(1-42) toxicity in synaptosomes. Nicotinamide, in particular, demonstrated a greater ability to suppress oxidative stress and apoptosis by enhancing antioxidant capacity and activating SIRT1. This research offers insights into potential therapeutic approaches for neurodegenerative diseases.

A Desert of Neurodegenerative Disease: Seeking Protective Solutions

Neurodegenerative diseases like Alzheimer's present a challenging landscape for researchers. This study offers promising results, suggesting that bexarotene and nicotinamide may offer neuroprotective benefits against Aβ toxicity. These findings provide hope for developing new therapeutic strategies to combat these debilitating diseases.

Dr.Camel's Conclusion

This study highlights the potential of bexarotene and nicotinamide as neuroprotective agents against Aβ(1-42) toxicity. The research provides valuable insights into potential therapeutic strategies for neurodegenerative diseases and underscores the need for further investigation into these promising compounds.

Date :
  1. Date Completed 2021-09-14
  2. Date Revised 2021-09-14
Further Info :

Pubmed ID

33428094

DOI: Digital Object Identifier

10.1007/s11064-020-03216-7

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English

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