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. 2011 Jan;48(1):26-32.
doi: 10.3164/jcbn.11-005FR. Epub 2010 Dec 29.

Lipoic acid: energy metabolism and redox regulation of transcription and cell signaling

Lester Packer  1 , Enrique Cadenas
Affiliations

Lipoic acid: energy metabolism and redox regulation of transcription and cell signaling

Lester Packer et al. J Clin Biochem Nutr. 2011 Jan.

Abstract

The role of R-α-lipoic acid as a cofactor (lipoyllysine) in mitochondrial energy metabolism is well established. Lipoic acid non-covalently bound and exogenously administered to cells or supplemented in the diet is a potent modulator of the cell's redox status. The diversity of beneficial effects of lipoic acid in a variety of tissues can be mechanistically viewed in terms of thiol/disulfide exchange reactions that modulate the environment's redox and energy status. Lipoic acid-driven thiol/disulfide exchange reactions appear critical for the modulation of proteins involved in cell signaling and transcription factors. This review emphasizes the effects of lipoic acid on PI3K and AMPK signaling and related transcriptional pathways that are integrated by PGC-1α, a critical regulator of energy homoestasis. The effects of lipoic acid on the neuronal energy-redox axis are largely reviewed in terms of their outcomes for aging and age-related neurodegenerative diseases.

Keywords: AMPK; PGC1α; dihydrolipoic acid; energy; insulin; lipoic acid; mitochondria; redox.

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Figures

Fig. 1
Fig. 1
Thiol/disulfide exchange by lipoic acid is the basis for its modulation of the cell’s energy and redox status.
Fig. 2
Fig. 2
Cellular uptake and release of lipoic acid and modification of the extracellular redox state.
Fig. 3
Fig. 3
Thiol/disulfide exchange as the basis for the activation/inhibition of cell signaling and transcription.
Fig. 4
Fig. 4
The insulin-like effect of lipoic acid and Akt-dependent stimulation of mitochondrial function.
Fig. 5
Fig. 5
Pyruvate dehydrogenase-catalyzed oxidative decarboxylation of pyruvate. The lipoyl moiety is shown in red. E1, a-ketoacid decarboxylase; E2, dihydrolipoyl transcetilase; E3, dihydrolipoyl dehydrogenase.
Fig. 6
Fig. 6
AMPK-dependent transcriptional pathway for PGC-1a activation.
See this image and copyright information in PMC

References

    1. Reed LJ, De BB, Gunsalus IC, Hornberger CS., Jr Crystalline alpha-lipoic acid; a catalytic agent associated with pyruvate dehydrogenase. Science. 1951;114:93–94. - PubMed
    1. Patel MS, Packer L, editors. Lipoid acid. energy production, antioxidant activity, and health effects. Boca Raton: CRC Press, Taylor & Francis Group; 2008.
    1. Shay KP, Moreau RF, Smith EJ, Smith AR, Hagen TM. Alpha-lipoic acid as a dietary supplement: molecular mechanisms and therapeutic potential. Biochim Biophys Acta. 2009;1790:1149–1160. - PMC - PubMed
    1. Koh EH, Cho EH, Kim MS, Park JY, Lee KU. Effects of alpha-lipoic acid on AMP-activated protein kinase in different tissues: therapeutic implications for the metabolic syndrome. In: Patel MS, Packer L, editors. Lipoic Acid: Energy Production, Antioxidant Activity, and Health Effects. Boca Raton, Florida: CRC Press/Taylor & Francis Group; 2008. pp. 495–519.
    1. Ziegler D. Painful diabetic neuropathy: advantage of novel drugs over old drugs? Diabetes Care. 2009;32(Suppl 2):S414–S419. - PMC - PubMed