Physiological overview of Human Ageing process

Authors

  • Christopher Joel Simon Graduate Student, Department of Prosthodontics, Saveetha Dental College, Saveetha Institute of Medical and Technical Sciences, Chennai, India. Author
  • Gayathri Assistant professor, Department of Physiology, Saveetha Dental College, Saveetha Institute of Medical and Technical Sciences, Chennai, India. Author
  • Revathy Duraisawamy Senior Lecturer, Department of Prosthodontics, Saveetha Dental College, Saveetha Institute of Medical and Technical Sciences, Chennai, India. Author
  • Dhanraj Ganapathy Professor and Head Department of Prosthodontics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical And Technical Sciences, Chennai – 600077 Tamil Nadu, India. Author

DOI:

https://doi.org/10.61841/ran37r63

Keywords:

ageing, physiology, senescence, changes, cells

Abstract

The impact that aging has on organisms is a complex interaction between the processes of aging at a cellular, organ, and integrated systems level and the effects of environmental factors such as nutrition, infection, and trauma. Physiologic aging involves changes that tend to be linear with time and are characteristically decremental in nature. A number of the functional changes can be delayed in onset or slowed in their progress by lifestyle. Aging challenges the reserves of function that allow for activity above the resting level and for regulation of the internal environment. Physiological changes occur with aging in all organ systems. The cardiac output decreases, blood pressure increases, and arteriosclerosis develops. The lungs show impaired gas exchange, a decrease in vital capacity, and slower expiratory flow rates. The creatinine clearance decreases with age, although the serum creatinine level remains relatively constant due to a proportionate age-related decrease in creatinine production. Functional changes, largely related to altered motility patterns, occur in the gastrointestinal system with senescence, and atrophic gastritis and altered hepatic drug metabolism are common in the elderly. Progressive elevation of blood glucose occurs with age on a multifactorial basis, and osteoporosis is frequently seen due to a linear decline in bone mass after the fourth decade. The epidermis of the skin atrophies with age, and due to changes in collagen and elastin, the skin loses its tone and elasticity. Lean body mass declines with age, and this is primarily due to loss and atrophy of muscle cells. Degenerative changes occur in many joints, and this, combined with the loss of muscle mass, inhibits elderly patients' locomotion. These changes with age have important practical implications for the clinical management of elderly patients. 

Downloads

Download data is not yet available.

References

1. Doherty TJ, Vandervoort AA, Brown WF. Effects of aging on the motor unit: a brief review. Canadian

Journal of Applied Physiology. 1993 Dec 1;18(4):331-58.

2. Dodds C. Physiology of aging. Anaesthesia & Intensive Care Medicine. 2006;7(12):456–458.

3. Sieck GC. Physiology of aging. J Appl Physiol (1985). 2003 Oct; 95(4):1333-4.

4. Davidovic M, Sevo G, Svorcan P, Milosevic DP, Despotovic N, Erceg P

Old age as a privilege of the "selfish ones." Aging Dis. 2010 Oct; 1(2):139-46.

5. van Heemst D. Insulin, IGF-1, and longevity. Aging and Disease. 2010;1:147–157.

6. Cornelius E. Increased incidence of lymphomas in thymectomized mice--evidence for an immunological

Theory of aging. Experientia. 1972;28:459.

7. Rozemuller AJ, van Gool WA, Eikelenboom P. The neuroinflammatory response in plaques and amyloid

Angiopathy in Alzheimer’s disease: therapeutic implications. Curr Drug Targets CNS Neurol Disord.

2005;4:223–23

8. Brys K, Vanfleteren JR, Braeckman BP. Testing the rate-of-living/oxidative damage theory of aging in the

nematode model Caenorhabditis elegans. Exp Gerontol. 2007;42:845–851.

9. Hulbert AJ, Pamplona R, Buffenstein R, Buttemer WA. Life and death: metabolic rate, membrane

composition and life span of animals. Physiol Rev. 2007;87:1175–1213.

10. Rollo CD. Aging and the Mammalian Regulatory Triumvirate. Aging and Disease. 2010;1:105–138.

11. Bjorksten J. The crosslinkage theory of aging. J Am Geriatr Soc. 1968;16:408–427.

12. Bjorksten J, Tenhu H. The crosslinking theory of aging--added evidence. Exp Gerontol. 1990;25:91–95.

13. Gerschman R, Gilbert DL, Nye SW, Dwyer P, Fenn WO. Oxygen poisoning and x-irradiation: a

mechanism in common. Science. 1954;119:623–626.

14. Harman D. Aging: a theory based on free radical and radiation chemistry. J Gerontol. 1956;11:298–300.

15. Afanas’ev I. Signaling and Damaging Functions of Free Radicals in Aging—Free Radical Theory,

Hormesis and TOR. Aging and Disease. 2010;1:75–88.

16. Cardiac function with age. Circulation 12:567-576, 1955.

17. Lakatta EG: Age-related alterations in the cardiovascular response to adrenergically mediated stress. Fed

Proc. 39:0015-0019, 1980.

18. Gerstenblith G, Lakatta EG, Weisfeldt ML: Age changes in myocardial function and exercise response. Prog Cardiovasc Dis 19:1-21, 1976.

19. Bader H: Dependence on wall stress in the human thoracic aorta of age and pressure. Circ Res 20:354-361, 1967.

20. Westermark P, Cornwell GG III, Johansson B, et al: Senile cardiac amyloidosis, In Glenner G, Costa P,

Freitas, F. (Eds.): Amyloid and Amyloidosis. Amsterdam, Elsevier, 1980, pp. 217-225.

21. Portman OW, Alexander M: Changes in arterial subfractions with aging and atherosclerosis. Biochem

Biophys Acta 2560:460-468, 1972.

22. Brady AW, Johnsen JR, Townley RG, et al.: The residual volume-predicted values as a function of age.

Am Rev Respir Dis 109:98-105, 1974.

23. Muresan G, Sorbini CA, Grassi V: Respiratory function in the aged. Bull Physio-Pathol Respir 7:973-

1007, 1971.

24. Dunnill MS, Halley W: Some observations on the quantitative anatomy of the kidney. J Pathol 110:113-

121, 1973.

25. Moore RA: Total number of glomeruli in the normal human kidney. Anat Rec 48:153-168, 1929.

26. Brocklehurst JC, Dillane JB, Griffiths J, et al: The prevalence and symptomatology of urinary infection

in an aged population. Gerontol Clin 10:242-253, 1968.

27. Wilson JD: The pathogenesis of prostatic hyperplasia. Am J Med 68:745-756, 1980.

28. Recker RR, Saville PD, Heavey RP: Effect of estrogens and calcium carbonate and bone loss in

postmenopausal women. Ann Intern Med 87:649-655, 1977 .

29. Weiss NS, Ure CL, Ballard JH, et al.: Decreased risk of fractures of the hip and lower forearm with postmenopausal use of estrogen. N Engl J Med 303:1195-1198, 1980.

30. Gilchrest BA: Some gerontologic considerations in the practice of dermatology. Arch Dermatol

115:1343-1346, 1979.

31. Selmanowitz WS, Rizer RL, Orentreich N: Aging of the skin and its appendages, in Finch, C, Hayflick L (Eds): Handbook of the Biology of Aging. New York, Van Nostrand Reinhold Co, 1977, pp. 496-509.

32. Rebeiz JJ, Moore MJ, Holden EM, et al.: Variations in muscle status with age and systemic diseases. Acta Neuropathol (Berlin) 22:127-144, 1972.

Downloads

Published

31.05.2020

How to Cite

Joel Simon, C., Gayathri, Duraisawamy, R., & Ganapathy, D. (2020). Physiological overview of Human Ageing process. International Journal of Psychosocial Rehabilitation, 24(3), 6657-6666. https://doi.org/10.61841/ran37r63