NAC seems to have a direct mineral chelating effect, meaning it can bind tightly to certain minerals and aid in their removal from the body. In rodents, decreased tissue accumulation and increased urinary excretion of lead has been observed following NAC supplementation,[1] and in humans, a reduction in serum lead has been found.[2] Standard oral doses of NAC appear to be protective against lead toxicity in humans, possibly related to a reduction in lead accumulation in the body and reducing oxidative stress.
Lead is a heavy mineral that can be toxic to the human body. Exposure to lead causes oxidative stress in the body, which seems to deplete both cellular and enzymatic antioxidants, including glutathione.[3] NAC is thought to alleviate the toxic effects of lead by aiding in its removal from the body while also acting as a building block for the synthesis of new glutathione.[1][4]
In animal studies, NAC has shown protective effects (assessed by biomarkers in serum and histopathological examination) against lead toxicity in the kidneys,[1] the brain,[4][5] and liver tissue.[5] In workers with high levels of occupational lead exposure, oral supplementation of 200–800 mg of N-acetylcysteine daily for 12 weeks reduced blood concentrations of lead and improved markers of oxidative stress.[2]
References
- ^Wang L, Wang Z, Liu JProtective effect of N-acetylcysteine on experimental chronic lead nephrotoxicity in immature female rats.Hum Exp Toxicol.(2010-Jul)
- ^Kasperczyk S, Dobrakowski M, Kasperczyk A, Ostałowska A, Birkner EThe administration of N-acetylcysteine reduces oxidative stress and regulates glutathione metabolism in the blood cells of workers exposed to leadClin Toxicol (Phila).(2013 Jul)
- ^Dobrakowski M, Pawlas N, Hudziec E, Kozłowska A, Mikołajczyk A, Birkner E, Kasperczyk SGlutathione, glutathione-related enzymes, and oxidative stress in individuals with subacute occupational exposure to lead.Environ Toxicol Pharmacol.(2016-Jul)
- ^Nehru B, Kanwar SSModulation by N-acetylcysteine of lead-induced alterations in rat brain: reduced glutathione levels and morphology.Toxicol Mech Methods.(2007)
- ^Ercal N, Treeratphan P, Hammond TC, Matthews RH, Grannemann NH, Spitz DRIn vivo indices of oxidative stress in lead-exposed C57BL/6 mice are reduced by treatment with meso-2,3-dimercaptosuccinic acid or N-acetylcysteine.Free Radic Biol Med.(1996)