• Log in with Facebook Log in with Twitter Log In with Google      Sign In    
  • Create Account
  LongeCity
              Advocacy & Research for Unlimited Lifespans

Photo
- - - - -

eNAMPT, aging delayed in older mice given this blood component from young mice

enampt mice aging nad+ nmn

  • This topic is locked This topic is locked
2 replies to this topic
⌛⇒ support MITOMOUSE via LongeCity!

#1 Engadin

  • Guest
  • 105 posts
  • 251
  • Location:Madrid
  • NO

Posted 13 June 2019 - 09:49 PM


S O U R C E :    Washington University School of Medicine

 

 

 

An enzyme in blood of young mice extends life span

 

 

 

Scientists are seeking new ways to extend healthy life spans, and a new study in mice suggests a novel strategy. Researchers at Washington University School of Medicine in St. Louis have shown that supplementing older mice with an enzyme called eNAMPT from younger mice extends life spans in the older mice. The active mouse in the video was given the enzyme; the less active mouse was given saline. The mice are the same age.

 

 

New research has identified a novel approach to staving off the detrimental effects of aging, according to a study from Washington University School of Medicine in St. Louis.

 

The study suggests that a protein that is abundant in the blood of young mice plays a vital role in keeping mice healthy. With age, levels of this protein decline in mice and people, while health problems such as insulin resistance, weight gain, cognitive decline and vision loss increase. Supplementing older mice with the protein obtained from younger mice appears to slow this decline in health and extend the life spans of older mice by about 16 percent.

 

The study is published June 13 in the journal Cell Metabolism.

 

The circulating protein is an enzyme called eNAMPT, which is known to orchestrate a key step in the process cells use to make energy. With age, the body’s cells become less and less efficient at producing this fuel — called NAD — which is required to keep the body healthy. Washington University researchers have shown that supplementing eNAMPT in older mice with that of younger mice appears to be one route to boosting NAD fuel production and keeping aging at bay.

 

“We have found a totally new pathway toward healthy aging,” said senior author Shin-ichiro Imai, MD, PhD, a professor of developmental biology. “That we can take eNAMPT from the blood of young mice and give it to older mice and see that the older mice show marked improvements in health — including increased physical activity and better sleep — is remarkable.”

 

Imai has long studied aging, using mice as stand-ins for people. Unlike other studies focused on transfusing whole blood from young mice to old mice, Imai’s group increased levels of a single blood component, eNAMPT, and showed its far-reaching effects, including improved insulin production, sleep quality, function of photoreceptors in the eye, and cognitive function in performance on memory tests, as well as increased running on a wheel. Imai’s group also has shown other ways to boost NAD levels in tissues throughout the body. Most notably, the researchers have studied the effects of giving oral doses of a molecule called NMN, the chemical eNAMPT produces. NMN is being tested in human clinical trials.

 

“We think the body has so many redundant systems to maintain proper NAD levels because it is so important,” Imai said. “Our work and others’ suggest it governs how long we live and how healthy we remain as we age. Since we know that NAD inevitably declines with age, whether in worms, fruit flies, mice or people, many researchers are interested in finding anti-aging interventions that might maintain NAD levels as we get older.”

 

Imai’s research has shown that the hypothalamus is a major control center for aging throughout the body, and it is directed in large part by eNAMPT, which is released into the blood from fat tissue. The hypothalamus governs vital processes such as body temperature, thirst, sleep, circadian rhythms and hormone levels. The researchers have shown that the hypothalamus manufactures NAD using eNAMPT that makes its way to the brain through the bloodstream after being released from fat tissue. They also showed that this eNAMPT is carried in small particles called extracellular vesicles. As levels of eNAMPT in the blood decline, the hypothalamus loses its ability to function properly, decreasing life span.

 

In an intriguing finding, Imai and first author Mitsukuni Yoshida, a doctoral student in Imai’s lab, showed that levels of eNAMPT in the blood were highly correlated with the number of days the mice lived. More eNAMPT meant a longer life span, and less meant a shorter one.

 

The researchers also showed increased life span with delivering eNAMPT to normal old mice. All mice that received saline solution as a control had died before day 881, about 2.4 years. Of the mice that received eNAMPT, one is still alive as of this writing, surpassing 1,029 days, or about 2.8 years.

 

“We could predict, with surprising accuracy, how long mice would live based on their levels of circulating eNAMPT,” Imai said. “We don’t know yet if this association is present in people, but it does suggest that eNAMPT levels should be studied further to see if it could be used as a potential biomarker of aging.”

 

The study also found sex differences in levels of eNAMPT, with female mice consistently showing higher levels of the enzyme.

 

“We were surprised by the dramatic differences between the old mice that received the eNAMPT of young mice and old mice that received saline as a control,” Imai said. “These are old mice with no special genetic modifications, and when supplemented with eNAMPT, their wheel-running behaviors, sleep patterns and physical appearance — thicker, shinier fur, for example — resemble that of young mice.”

 

Imai and his colleagues, including co-author Rajendra Apte, MD, PhD, the Paul A. Cibis Distinguished Professor of Ophthalmology and Visual Sciences, noted that eNAMPT also is carried in extracellular vesicles in humans. As such, future studies should be done to investigate whether low levels are associated with disease in aging people and whether supplementing eNAMPT in extracellular vesicles could serve as an anti-aging intervention in older people, they said.

 

 

 


  • Informative x 2

#2 Fafner55

  • Member
  • 227 posts
  • 219
  • Location:USA
  • NO

Posted 13 June 2019 - 10:58 PM

Watson and Giuliano describe eNAMPT as a dangerous, proinflammatory cytokine.

 

“Part 5 of the NAD world: the conflicting roles of NAMPT – inflammation or rescue? Also Part 1 on a new series on inflammation” (2016-05) http://www.anti-agin...n-inflammation/


  • Informative x 1

#3 Michael

  • Advisor, Moderator
  • 1,251 posts
  • 1,719
  • Location:Location Location

Posted 14 June 2019 - 03:03 AM

"The researchers also showed increased life span with delivering eNAMPT to normal old mice. All mice that received saline solution as a control had died before day 881, about 2.4 years. Of the mice that received eNAMPT, one is still alive as of this writing, surpassing 1,029 days, or about 2.8 years."

 

I haven't yet read the full text, but if that summary is acccurate, this part of the report at least is a complete joke. As I have repeated ad nauseum, the cardinal sin of biogerontology is the use of short-lived controls, and this is apparently another infraction.

A cohort of normal, healthy, well-husbanded, non-genetically-fucked-up mice will have on average lifespan >800 days, and a maximum lifespan (tenth-decile survivorship) >1000 d, as is routine in the standard control groups in studies run by people who know what they're doing (Spindler, Weindruch, Miller, etc).Here, all the control mice were dead at an age where very approximately half of them should still have been alive, and all but one of the treated mice died before the age when 10% of the controls should still have been alive!

Whether it's buggered-up mutants that die early of things of purely putative mechanistic or structural significance to 'normal' aging, or (most commonly -- resveratrol and many others) diabetic obesity from overfeeding, or malnourishment, or failing to keep a good lid on pathogens, you raise a colony in whicih ALL the animals are short-lived, by incompetence or by design; then if your intervention helps to partially normalize their miserably short lives, you proclaim a radical life-extension breakthrough.

 

Sigh.

 

I'm generally impressed by Imai's work, but at the very least this part of this study is of no value, and it makes me suspect that a lot of what they're claiming to be rejuvenating effects in "old" mice actually was perfectly normal for what were actually middle aged mice.

 

 

 


  • Informative x 3
  • Agree x 1

⌛⇒ support MITOMOUSE via LongeCity!




0 user(s) are reading this topic

0 members, 0 guests, 0 anonymous users