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[FightAging] An Overview of Inflammaging and Mitochondrial Damage


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#1 ImmInst

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Posted 10 March 2012 - 12:45 AM


With advancing age - and accumulating damage - the immune system moves into a state wherein it is constantly roused and on alert, exacting a toll on the integrity of tissue and cells through its signaling and activity, but also ineffective at actually tackling pathogens, senescent cells, precancerous cells, and other things that should be destroyed. So you have constant chronic inflammation and all its downsides with none of the compensatory immune activity boost that comes with short-term inflammation in the young. Researchers have given the name "inflammaging" to this progressive and increasingly harmful disarray of the immune system, and you'll find a few introductions to inflammaging as a concept back in the Fight Aging! archives.

Below is an open access paper that gives an overview of inflammaging and how it relates to some of the forms of cellular damage that cause aging. In this paper, the researchers paint a picture of inflammaging derived from root causes that involve mitochondrial damage and progressive failure of autophagy to clear out that damage, two line items that have been examined a fair number of times here in the past - under the Strategies for Engineered Negligible Senescence (SENS) viewpoint these two are amongst the fundamental, root causes of aging.

Inflammaging: disturbed interplay between autophagy and inflammasomes

In 2000, Franceschi et al. coined the term "inflammaging" in order to refer to a low-grade pro-inflammatory status appearing during the aging process. They emphasized the role of macrophages as well as cellular stress and genetic factors in the generation of the inflammaging condition. In addition, they hypothesized that this inflammatory environment could predispose the organism to the development of several age-related diseases. During recent years, this scenario has been confirmed by a plethora of experimental evidence. ... Interestingly, the aging process is simultaneously accompanied by both the features accelerating inflammaging and the counteracting, so-called anti-inflammaging characteristics. It seems that the balance between these opposite forces controls the outcome of the aging process, either leading to frailty and degenerative diseases or a healthy old age and longevity.

...

The aging process is associated with a decline in autophagic capacity which impairs cellular housekeeping, leading to protein aggregation and accumulation of dysfunctional mitochondria which provoke reactive oxygen species (ROS) production and oxidative stress.

Recent studies have clearly indicated that the ROS production induced by damaged mitochondria can stimulate intracellular danger-sensing multiprotein platforms called inflammasomes. [As a result of inflammasome activity, signaling molecules called] cytokines provoke inflammatory responses and accelerate the aging process by inhibiting autophagy.

There has been some good progress in recent years in pulling things together in the big picture - and the more that we see the mechanisms of SENS featured, the better to my eyes. That ways lies increased support for rejuvenation biotechnology that will actually work to reverse aging, rather than the present mainstream course of aiming to slow down aging just a little sometime in next few decades.


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#2 albedo

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Posted 26 October 2014 - 01:24 PM

Bumping this up. Two informations:

 

1. A short Ben Best reports on Dr Claudio Franceschi talk at the recent Sochi conference (last issue Nov. 2014 of LEF magazine):

"....Claudio Franceschi, MD, (Professor, University of Bologna, Bologna, Italy) is noteworthy in aging research for promoting the inflammation theory of aging―and for coining the term “inflammaging.” Acute inflammation can repair injured tissues and eliminate attacking microorganisms. But aging is too often characterized by chronic inflammation that is damaging rather than beneficial.

In his presentation, Dr. Franceschi provided evidence for the use of inflammation symptoms as a means of determining biological age, as distinct from chronological age: a biomarker of aging. A biomarker of aging would be useful for determining if drugs or other interventions intended to slow aging are effective.1

Dr.Franceschi has conducted many studies on people of many ages, but particularly has studied people who have lived extremely long lives. He and others have found that glycosylation (linkage of sugars to proteins) is a biomarker of aging that contributes to inflammation.1-3 Other biomarkers of aging that hehas found are epigenetic changes (certain changes in gene expression)4 and changes in amino acids and blood lipids.5,6 Concerning the latter, Dr.Franceschi cited a study showing that a vegetarian, high-fiber diet can reduce cardiovascular disease.7….”

http://www.lef.org/m...sia/page-01?p=1

 

2. A very dense presentation from Dr. Claudio Franceschi et al. on Inflammaging theory, the EU's NU-AGE project, microbiome, dysbiosis and links with disease is here.

 


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