Mitochondrial Dysfunction in Skeletal Muscle of Rotenone-Induced Rat Model of Parkinson's Disease: SC- Nanophytosomes as Therapeutic Approach

Int J Mol Sci. 2023 Nov 27;24(23):16787. doi: 10.3390/ijms242316787.

Abstract

The development of new therapeutic options for Parkinson's disease (PD) requires formulations able to mitigate both brain degeneration and motor dysfunctions. SC-Nanophytosomes, an oral mitochondria-targeted formulation developed with Codium tomentosum membrane polar lipids and elderberry anthocyanin-enriched extract, promote significant brain benefits on a rotenone-induced rat model of PD. In the present work, the effects of SC-Nanophytosome treatment on the skeletal muscle tissues are disclosed. It is unveiled that the rotenone-induced PD rat model exhibits motor disabilities and skeletal muscle tissues with deficient activity of mitochondrial complexes I and II along with small changes in antioxidant enzyme activity and skeletal muscle lipidome. SC-Nanophytosome treatment mitigates the impairment of complexes I and II activity, improving the mitochondrial respiratory chain performance at levels that surpass the control. Therefore, SC-Nanophytosome competence to overcome the PD-related motor disabilities should be also associated with its positive outcomes on skeletal muscle mitochondria. Providing a cellular environment with more reduced redox potential, SC-Nanophytosome treatment improves the skeletal muscle tissue's ability to deal with oxidative stress stimuli. The PD-related small changes on skeletal muscle lipidome were also counteracted by SC-Nanophytosome treatment. Thus, the present results reinforces the concept of SC-Nanophytosomes as a mitochondria-targeted therapy to address the neurodegeneration challenge.

Keywords: Parkinson’s disease; algae polar lipids; elderberry anthocyanins; mitochondrial dysfunction; nanomedicine; skeletal muscle.

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Mitochondrial Diseases*
  • Muscle, Skeletal
  • Neuroprotective Agents* / pharmacology
  • Oxidative Stress
  • Parkinson Disease* / drug therapy
  • Parkinson Disease* / etiology
  • Rats
  • Rotenone / pharmacology

Substances

  • Rotenone
  • Antioxidants
  • Neuroprotective Agents