Combinatorial glucose, nicotinic acid and N-acetylcysteine therapy has synergistic effect in preclinical C. elegans and zebrafish models of mitochondrial complex I disease.
Sujay GuhaNeal D MathewChigoziri KonkwoJulian OstrovskyYoung Joon KwonErzsebet PolyakChristoph SeilerMichael BennettRui XiaoZhe ZhangEiko Nakamaru-OgisoMarni J FalkPublished in: Human molecular genetics (2022)
Mitochondrial respiratory chain disorders are empirically managed with variable antioxidant, cofactor and vitamin 'cocktails'. However, clinical trial validated and approved compounds, or doses, do not exist for any single or combinatorial mitochondrial disease therapy. Here, we sought to pre-clinically evaluate whether rationally designed mitochondrial medicine combinatorial regimens might synergistically improve survival, health and physiology in translational animal models of respiratory chain complex I disease. Having previously demonstrated that gas-1(fc21) complex I subunit ndufs2-/-C. elegans have short lifespan that can be significantly rescued with 17 different metabolic modifiers, signaling modifiers or antioxidants, here we evaluated 11 random combinations of these three treatment classes on gas-1(fc21) lifespan. Synergistic rescue occurred only with glucose, nicotinic acid and N-acetylcysteine (Glu + NA + NAC), yielding improved mitochondrial membrane potential that reflects integrated respiratory chain function, without exacerbating oxidative stress, and while reducing mitochondrial stress (UPRmt) and improving intermediary metabolic disruptions at the levels of the transcriptome, steady-state metabolites and intermediary metabolic flux. Equimolar Glu + NA + NAC dosing in a zebrafish vertebrate model of rotenone-based complex I inhibition synergistically rescued larval activity, brain death, lactate, ATP and glutathione levels. Overall, these data provide objective preclinical evidence in two evolutionary-divergent animal models of mitochondrial complex I disease to demonstrate that combinatorial Glu + NA + NAC therapy significantly improved animal resiliency, even in the face of stressors that cause severe metabolic deficiency, thereby preventing acute neurologic and biochemical decompensation. Clinical trials are warranted to evaluate the efficacy of this lead combinatorial therapy regimen to improve resiliency and health outcomes in human subjects with mitochondrial disease.
Keyphrases
- oxidative stress
- clinical trial
- transcription factor
- dna damage
- endothelial cells
- cell therapy
- healthcare
- ischemia reperfusion injury
- diabetic rats
- induced apoptosis
- signaling pathway
- ms ms
- multiple sclerosis
- mental health
- open label
- drug delivery
- genome wide
- liver failure
- electronic health record
- early onset
- randomized controlled trial
- blood pressure
- gene expression
- risk assessment
- intensive care unit
- phase ii
- metabolic syndrome
- resting state
- white matter
- smoking cessation
- insulin resistance
- room temperature
- adipose tissue
- dna methylation
- cancer therapy
- acute respiratory distress syndrome
- ionic liquid
- free survival
- social media
- study protocol
- bone marrow
- extracorporeal membrane oxygenation
- endoplasmic reticulum stress
- heat shock protein