Regulatory effects of dihydrolipoic acid against inorganic mercury-mediated cytotoxicity and intrinsic apoptosis in PC12 cells.

Autor: Binte Hossain, Kaniz Fatima1 (AUTHOR), Rahman, Md Mostafizur2,3 (AUTHOR), Sikder, Md Tajuddin2,4 (AUTHOR), Hosokawa, Toshiyuki5 (AUTHOR), Saito, Takeshi6 (AUTHOR), Kurasaki, Masaaki1,2 (AUTHOR) kura@ees.hokudai.ac.jp
Předmět:
Zdroj: Ecotoxicology & Environmental Safety. Apr2020, Vol. 192, pN.PAG-N.PAG. 1p.
Abstrakt: Mercury (Hg) is an extremely dangerous environmental contaminant, responsible for human diseases including neurological disorders. However, the mechanisms of inorganic Hg (iHg)- induced cell death and toxicity are little known. Dihydrolipoic acid (DHLA) is the reduced form of a naturally occurring compound lipoic acid, which act as a potent antioxidant through multiple mechanisms. So we hypothesized that DHLA has an inhibitory role on iHg-cytotoxicity. The purposes of this research were to investigate mechanism/s of cytotoxicity of iHg, as well as, the cyto-protection of DHLA against iHg induced toxicity using PC12 cells. Treatment of PC12 cells with HgCl 2 (Hg2+) (0–2.5 μM) for 48 h resulted in significant toxic effects, such as, cell viability loss, high level of lactate dehydrogenase (LDH) release, DNA damage, cellular glutathione (GSH) level decrease and increased Hg accumulation. In addition, protein level expressions of akt, p-akt, mTOR, GR, NFkB, ERK1, Nrf2 and HO-1 in cells were downregulated; and cleaved caspase 3 and cytochrome c release were upregulated after Hg2+ (2.5 μM) exposure and thus inducing apoptosis. Hg2+induced apoptosis was also confirmed by flow cytometry. However, pretreatment with DHLA (50 μM) for 3 h before Hg2+ (2.5 μM) exposure showed inhibition against iHg2+-induced cytotoxicity by reversing cell viability loss, LDH release, DNA damage, GSH decrease and inhibiting Hg accumulation. Moreover, DHLA pretreatment reversed the protein level expressions of akt, p-akt, mTOR, GR, NFkB, ERK1, Nrf2, HO-1, cleaved caspase 3 and cytochrome c. In conclusion, results showed that DHLA could attenuate Hg2+-induced cytotoxicity via limiting Hg accumulation, boosting up of antioxidant defense, and inhibition of apoptosis in cells. Image 1 • Inorganic Hg2+ has toxic effects in PC12 cells, even in a small concentration. • Inorganic Hg induced apoptosis via intrinsic pathway in PC12 cells. • Pre-treatment of DHLA attenuates Hg−induced apoptosis through its antioxidant properties. [ABSTRACT FROM AUTHOR]
Databáze: GreenFILE