Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Apr;8(4):589-602.
doi: 10.18632/aging.100931.

Principles of alternative gerontology

Affiliations
Review

Principles of alternative gerontology

Tomasz Bilinski et al. Aging (Albany NY). 2016 Apr.

Abstract

Surveys of taxonomic groups of animals have shown that contrary to the opinion of most gerontologists aging is not a genuine trait. The process of aging is not universal and its mechanisms have not been widely conserved among species. All life forms are subject to extrinsic and intrinsic destructive forces. Destructive effects of stochastic events are visible only when allowed by the specific life program of an organism. Effective life programs of immortality and high longevity eliminate the impact of unavoidable damage. Organisms that are capable of agametic reproduction are biologically immortal. Mortality of an organism is clearly associated with terminal specialisation in sexual reproduction. The longevity phenotype that is not accompanied by symptoms of senescence has been observed in those groups of animals that continue to increase their body size after reaching sexual maturity. This is the result of enormous regeneration abilities of both of the above-mentioned groups. Senescence is observed when: (i) an organism by principle switches off the expression of existing growth and regeneration programs, as in the case of imago formation in insect development; (ii) particular programs of growth and regeneration of progenitors are irreversibly lost, either partially or in their entirety, in mammals and birds.

Keywords: aging; energy; growth; life program; longevity; regeneration; senescence.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest statement

The authors declare that they have no conflict of interest.

Figures

Figure 1
Figure 1. The senescence phenotype types among various animal clades
Symbols and abbreviations: 1 - Type of senescence (Bi - biologically immortal, nS - mortal: nonsenescent, Se - mortal: senescent); 2 - Growth (body size increase of adults) and regenerative abilities (GR - constant growth and high regeneration, NR - no growth and high regeneration, NL - no growth and low regeneration, NN - no growth and no regeneration); 3 - Lifespan (L - long, i - intermediate, S - short); Pisces - Classes: Chondrichthyes, Sarcopterygii and Actinopterygii.
Figure 2
Figure 2. The relationship between senescence and life program connected with the ability to cell replacement and regeneration
pcd – proximal cause of death.

Similar articles

Cited by

References

    1. Partridge L. The new biology of ageing. Philosophical transactions of the Royal Society of London Series B, Biological sciences. 2010;365:147–154. - PMC - PubMed
    1. Partridge L, Thornton J, Bates G. The new science of ageing. Philosophical transactions of the Royal Society of London Series B, Biological sciences. 2011;366:6–8. - PMC - PubMed
    1. Holliday R, Rattan SIS. Longevity mutants do not establish any “new science” of ageing. Biogerontology. 2010;11:507–511. - PubMed
    1. Bilinski T, Paszkiewicz T, Zadrag-Tecza R. Energy excess is the main cause of accelerated aging of mammals. Oncotarget. 2015;6:12909–12919. doi: 10.18632/oncotarget.4271. - DOI - PMC - PubMed
    1. Bilinski T, Zadrag-Tecza R. The rules of aging: are they universal? Is the yeast model relevant for gerontology? Acta biochimica Polonica. 2014;61:663–669. - PubMed

Publication types