Introduction:A recent approach to cure neurodegenerative diseases is to reprogram fibroblasts into functioning neurons using multiple exogenous transcription factors (TFs) and micro-RNAs. Administering agents that can endogenously induce these TFs may bypass the limitations of this approach. Astrocytes may represent a part of the extrahepatic-stellate system involved in vitamin-A (V A ) homeostasis. Activatedstellate cells lose their V A -storage capacity, and this was previously applied for hepaticstellate cells (HSCs) targeting to treat liver fibrosis. Accordingly, it is hypothesized that Parkinson's disease (PD) may be coupled with retinoid depletion that may extract V A from V A -rich-HSCs triggering liver fibrosis. Thus, V A administration may selectively target V A -deficient reactive astrocytes and HSCs. Besides, V A has the regenerative capability and may induce endogenous-TFs generation.Methods: Fluorescently labeled V A -coupled liposomes (FLV) were traced using confocal laser microscope in rats with induced PD for detecting brain accumulation and uptake into fluorescently labeled astrocytes. Liver fibrosis associated with PD was assessed biochemically and histopathologically, while V A deficiency was confirmed by assessing retinol-binding protein gene expression in the brain and liver. Multiple V A doses were tested for reversing PD-associated liver fibrosis, generating TFs (involved in reprograming astrocytes/fibroblasts into different neuronal types) and capability of dopaminergic-neurons regeneration.Results: Fluorescently labeled V A -coupled liposomes revealed selective brain accumulation and uptake into astrocytes. PD was associated with significant liver fibrosis and V A deficiency in the brain and liver. Furthermore, V A -medium dose (VAMD) was the optimum one for reversing PD-associated liver fibrosis, generating multiple astrocytes/fibroblasts reprogramming TFs, regenerating dopaminergic neurons, and improving PD.