Friday, December 13, 2013

Avoiding the retirement home: How aging impacts regeneration in two separate body systems


                Aging has always been a major discussion for society as far as what it means and if we should treat it. The process of aging, or senescence, is sometimes treated negatively in our society.  From senility to dependence on others, older individuals are sometimes perceived as detriments to society.  In order to avoid such a social stigma, aging is something that is actively avoided.  We try our best to stay young and healthy and attempt to avoid detriments in our physical and mental abilities. In an effort to understand the impacts of aging many researchers have performed experiments that prove to be useful in comprehending age effects.
                In the paper, “Regeneration of New Neurons is Preserved in Aged Vomeronasal Epithelia” by Dr. Jessica Brann and Dr. Stuart Firestein, the impacts of age on mice.  During a seminar through Loyola University Chicago’s Neuroscience Seminar series, Dr. Brann gave a lecture on how the vomeronasal organ had the capacity to produce a lifelong proliferation of the neurons.  This is significant because the nervous system typically has a difficult time completing neurogenesis and is isolated to particular segments of the nervous system.  Using BrdU, an analog of tymidine as a cell proliferation marker, Brann and Firestein, observed that neurogenesis and repair of neurons remained similar in young and old mice (18-24 months). The significance of this research showed that, there was a particular part of the body (vomeronasal organ) whose regenerative functions were not impaired by the effects of age.
                Not all parts of the body behave this way- having the ability to regenerate sufficiently with increasing age. “Impact of Age on Liver Regeneration Response to Injury After Partial Hepactectomy in a Rat Model” an article by Sanchez-Hidalgo et al. demonstrate the effects of age on hepatogenesis. In the Sanchez-Hidalgo experiments, hepatectomies were performed on rat subjects that were distinguished by age (young at 4-7 months and old at 24-27 months).  Regeneration measurements of the liver tissue were performed by allowing regeneration time of 6 to 48 hours after surgery and weighing the remaining liver after sacrifice (comparison with estimated starting liver size).  Sanchez-Hidalgo et al. observed that there was significant impairment of liver regeneration for older rats versus younger rats.
                Age-resistant regenerative techniques will have considerable impact on the future of medicine and our perceptions of age.  With Dr. Brann’s research, we understand that a particular part of the mouse’s nervous system has the capacity to undergo neurogenesis without age playing a factor on how well this regenerative function is performed.  Even though Dr. Brann and Sanchez-Hidalgo both examined the differences of regeneration of nervous and liver tissue respectively, they found different results off age-dependent regeneration.  If one understood why the effects of the vomeronasal organ are age-resistant compared to the age-dependent regeneration of the hepatic tissue or other parts of the nervous system, a potential new treatment for age-related diseases could be created in order to stop or slow down the negative impacts of aging.  With that, we would potentially be able to treat age-related disease and our negative perceptions of old age.


Brann, Jessica H., and Stuart Firestein. "Regeneration of New Neurons Is Preserved in Aged Vomeronasal Epithelia." The Journal of Neuroscience 30.46 (2010): 15686-94. Web. 10 Dec. 2013


Sanchez-Hidalgo, Juan M., Alvaro Naranjo, Isidora Ranchal, Patricia Aguilar-Melero, and Gustavo Ferrin. "Impact of Age on Liver Regeneration Response to Injury After Partial Hepatectomy in a Rat Model." Journal of Surgical Research 175.1 (2012): 1-9. Web. 11 Dec. 2013.

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