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Nonetheless, when a cell (e.g., a hepatocyte) is exposed to inflammation or oxidative stress, NRF-2 has the capacity to escape from regulation by KEAP1 through the increase in the transcription of mRNA from NRF-2, with the objective of depleting the reserves of KEAP1, which cannot be recycled because of the suppression of another NRF-2 [21]

Some also raise questions and concerns about compounded options, highlighting the uncertainty people feel when affordability becomes a treatment barrier

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doi:10.1007/BF02179289CrossRefGoogle ScholarPubMed Research Units on Pediatric Psychopharmacology Autism Network

Bulletin of Experimental Biology and Medicine, 158 , 726-728