Emerging Potential of the Phosphodiesterase (PDE) Inhibitor Ibudilast for Neurodegenerative Diseases: An Update on Preclinical and Clinical Evidence.
Efthalia AngelopoulouEfstratios-Stylianos PyrgelisChristina PiperiPublished in: Molecules (Basel, Switzerland) (2022)
Neurodegenerative diseases constitute a broad range of central nervous system disorders, characterized by neuronal degeneration. Alzheimer's disease, Parkinson's disease, amyolotrophic lateral sclerosis (ALS), and progressive forms of multiple sclerosis (MS) are some of the most frequent neurodegenerative diseases. Despite their diversity, these diseases share some common pathophysiological mechanisms: the abnormal aggregation of disease-related misfolded proteins, autophagosome-lysosome pathway dysregulation, impaired ubiquitin-proteasome system, oxidative damage, mitochondrial dysfunction and excessive neuroinflammation. There is still no effective drug that could halt the progression of neurodegenerative diseases, and the current treatments are mainly symptomatic. In this regard, the development of novel multi-target pharmaceutical approaches presents an attractive therapeutic strategy. Ibudilast, an anti-inflammatory drug firstly developed as an asthma treatment, is a cyclic nucleotide phosphodiesterases (PDEs) inhibitor, which mainly acts by increasing the amount of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), while downregulating the pro-inflammatory factors, such as tumor necrosis factor-α (TNF-α), macrophage migration inhibitory factor (MIF) and Toll-like receptor 4 (TLR-4). The preclinical evidence shows that ibudilast may act neuroprotectively in neurodegenerative diseases, by suppressing neuroinflammation, inhibiting apoptosis, regulating the mitochondrial function and by affecting the ubiquitin-proteasome and autophagosome-lysosome pathways, as well as by attenuating oxidative stress. The clinical trials in ALS and progressive MS also show some promising results. Herein, we aim to provide an update on the emerging preclinical and clinical evidence on the therapeutic potential of ibudilast in these disorders, discuss the potential challenges and suggest the future directions.
Keyphrases
- multiple sclerosis
- toll like receptor
- oxidative stress
- inflammatory response
- clinical trial
- rheumatoid arthritis
- mass spectrometry
- lipopolysaccharide induced
- anti inflammatory
- immune response
- nuclear factor
- lps induced
- white matter
- cell therapy
- traumatic brain injury
- cerebral ischemia
- dna damage
- ms ms
- adipose tissue
- cognitive impairment
- chronic obstructive pulmonary disease
- protein kinase
- fluorescent probe
- endoplasmic reticulum stress
- living cells
- cell death
- minimally invasive
- stem cells
- physical activity
- bone marrow
- subarachnoid hemorrhage
- brain injury
- binding protein
- study protocol
- single molecule
- cell proliferation
- induced apoptosis
- heat shock protein
- mild cognitive impairment
- heat stress