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  2. Discovery of neuroprotective Agents: Potent, brain Penetrating, lipoic acid derivatives for the potential treatment of ischemic stroke by regulating oxidative stress and inflammation - a Preliminary study

Discovery of neuroprotective Agents: Potent, brain Penetrating, lipoic acid derivatives for the potential treatment of ischemic stroke by regulating oxidative stress and inflammation - a Preliminary study

  • Bioorg Chem. 2024 Jun:147:107339. doi: 10.1016/j.bioorg.2024.107339.
Chenchen Zhu 1 Yun Wang 1 Yi Li 1 Tingfang Wang 1 Fei Ye 1 Wei Su 1 Ting Chen 2 Chuan Zhang 3 Liyan Xiong 4
Affiliations

Affiliations

  • 1 Shanghai Baoshan Luodian hospital, School of Medicine, Shanghai University, Shanghai 201908, China.
  • 2 Shanghai Baoshan Luodian hospital, School of Medicine, Shanghai University, Shanghai 201908, China. Electronic address: cttc1990@126.com.
  • 3 Shanghai Baoshan Luodian hospital, School of Medicine, Shanghai University, Shanghai 201908, China. Electronic address: zc843016@shu.edu.cn.
  • 4 Shanghai Baoshan Luodian hospital, School of Medicine, Shanghai University, Shanghai 201908, China. Electronic address: xiongly@shu.edu.cn.
Abstract

Stroke poses a serious risk to the physical and mental health of patients. Endogenous compounds are widely used to treat ischemic stroke. Lipoic acid, a naturally occurring (R)-5-(1,2-dithiolan-3-yl)pentanoic acid, has therapeutic potential for the treatment of ischemic stroke. However, the direct application of lipoic acid is limited by its relatively low efficacy and instability. Therefore, there is a need to modify the structure of lipoic acid to improve its pharmaceutical capabilities. Currently, 37 lipoic acid derivatives have been synthesized, and compound AA-9 demonstrated optimal therapeutic potential in an in vitro model of induced oxidative damage using tert-butyl hydroperoxide (t-BHP). In addition, in vitro experiments have shown that compound AA-9 has an excellent safety profile. Subsequently, the therapeutic effect of AA-9 was significant in the rat MCAO ischemic stroke model, which may be attributed to the antioxidant and anti-inflammatory effects of compound AA-9 by activating PGC-1α and inhibiting NLRP3. Notably, compound AA-9 exhibited higher stability and better bioavailability properties than ALA in plasma stability and pharmacokinetic properties. In conclusion, AA-9 may be a promising neuroprotective agent for the treatment of ischemic stroke and warrants further investigation.

Keywords

Lipoic acid derivatives; Pharmacokinetic properties; Plasma stability; Stroke; Synergistic therapy.

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