Most evidence indicates that aging is a result of normal metabolic pro
cesses that are essential for life. Thus an important approach in biog
erontology is to identify specific metabolic reactions necessary for l
ife but which could also lead to aging. A unique characteristic of thi
s approach is an explanation of what governs aging rate or longevity o
f a species or even individuals within a species. These would be mecha
nisms that would act to reduce the long-term toxic or aging effects of
the normal metabolic and developmental reactions. The reactions invol
ving oxygen metabolism clearly fit into this model for they are essent
ial for life yet can potentially cause many of the dysfunctions associ
ated with aging. Such a model can also account for differences in agin
g rate or longevity of different animal species by differences that ma
y exist in their innate ability to reduce oxidative stress state. Our
laboratory has been testing this oxidative stress state (OSS) hypothes
is of aging and longevity by determining if a positive correlation exi
sts between OSS of an animal and its aging rate. Much of our data has
found such a positive correlation, yet there is some indication that s
eparate causative mechanisms may exist in determining aging rate as op
posed to those related to age-dependent specific diseases such as canc
er or cardiovascular disease.