Table 1.
Year | Key finding | Reference |
---|---|---|
1954 | Gerschman and coworkers notes oxygen poisoning resembles X-ray damage and propose free radical involvement |
[1] |
1956 | Harman proposes the free radical theory of aging | [2] |
1958 | Szent-Gyorgyi proposed involvement of free radicals in biological systems | [5] |
1967 | Esterbauer describes the production of 4-hydroxy-2-nonenal (HNE) | [66] |
1969 | McCord and Fridovich discover superoxide dismutase | [3] |
1970 | Meister describes the γ-glutamyl cycle in glutathione biosynthesis | [34] |
1972 | Boveris Oshino, and Chance discover production of H2O2 by mitochondria | [16] |
1973 | Babior and coworkers demonstrate O2 production by phagocytes | [30] |
1974 | Two labs demonstrate O2 production by mitochondrial respiratory chain | [17,18] |
1974 | Crapo and Tierney demonstrate adaptation to hyperoxia in rats correlates with increased superoxide dismutase |
[26] |
1976 | Cadenas and Boveris show that ubisemiquinone oxidation is the source of mitochondrial O2·− |
[19] |
1977 | Murad demonstrates nitric oxide induction of cyclic GMP | [106] |
1979 | Ignarro demonstrates muscle relaxation by nitro compounds including NO | [107] |
1981 | Furchgott describes endothelial derived relaxing factor (EDRF) | [108] |
1983 | Lands demonstrates peroxide tone regulates cyclooxygenase | [44] |
1984- 1985 |
Comporti, Dianzani, Poli, Slater, and Esterbauer demonstrate pathology due to HNE | [66,67] [70] |
1985 | Sies defines oxidative stress | [35] |
1987 | Poli demonstrates that HNE acts as a stimulant of signaling | [72] |
1989 | Gopalakrishna and Anderson demonstrate H2O2 activation of classical protein kinase C | [43] |
1991 | Schreck and coworkers demonstrate NF-κB activation by addition of exogenous H2O2 to lymphocytes |
[50] |
1991 | Rushmore and Pickett discover the antioxidant response element (aka EpRE) | [79] |
1994 | Forman and coworkers demonstrate that quinones induce glutamate cysteine ligase (GCL) | [38] |
1995 | Mulcahy and coworkers show that EpRE regulates | [81] |
1996 | Kaul and Forman demonstrate activation of NFκB by endogenously generated H2O2 in macrophages |
[51] |
1996 | Venugopal and Jaiswal identify Nrf2 as regulator of EpRE | [109] |
1998 | Denu and Tanner demonstrate reversible inactivation of PTP1B by H2O2 | [110] |
1999 | Lambeth and coworkers discover the NOX DuOX family of enzymes is found in almost all cells |
[55] |
1999 | Chock demonstrates glutathionylation of PTP1B | [111] |
2001 | Kensler, Yamamoto and coworkers demonstrate link of Nrf2 deficiency to carcinogenesis | [112] |
2002 | Talalay, Yamamoto, and coworkers demonstrate Keap1 modification by electrophiles | [113] |
2003 | Nel and coworkers demonstrate a role for oxidants in signaling by air pollution particle exacerbation of asthma |
[114] |
2003 | Yamamoto, Hayes and coworkers demonstrate Keap1 facilitates Nrf2 degradation | [115] |
2004 | Levonen, Darley-Usmar and coworkers show HNE conjugates to Keap1 | [116] |
2004 | Hagen and coworkers demonstrate loss of Nrf2 signaling in aging | [100] |
2006 | Forman and coworkers demonstrate selective and reversible PTP1B glutathionylation during signaling |
[90] |