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Can N-acetyl-DL-leucine really help people's eyes from losing visual acuity as they age?

n-acetyl-dl-leucine eyes

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#1 MrSpud

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Posted 31 October 2015 - 03:50 PM


This patent https://www.google.c...AIVxBY-Ch2EYQwQ says:

The invention relates to a medicament, the active principle of which is a leucine and, for example, a N-ACETYL-DL-LEUCINE. It can be applied to the prevention and/or treatment of eye diseases or disorders and especially of hereditary dystrophies of the retina, glaucomatous neuropathy, glaucoma, macular degeneration, myopia, presbyopia, hypermetropia, astigmatism, all the ophtalmologic diseases or disorders inducing a decrease of visual function and/or age-related physiological vision decline.

Do you think this stuff would really work to help keep the eyes from going bad as people age?

#2 zorba990

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Posted 25 December 2020 - 02:05 AM

I just ran across this compound Acetyl Leucine here (so would be great if some supplement manufacturer would pick it up in bulk, since enhancing lysosomes should work synergistically with up regulating autophagy, and perhaps injury recovery as well) :

Acetyl-leucine slows disease progression in lysosomal storage disorders
https://academic.oup...fcaa148/5906021

"Abstract
Acetyl-DL-leucine is a derivative of the branched chain amino acid leucine. In observational clinical studies acetyl-DL-leucine improved symptoms of ataxia, in particular in patients with the lysosomal storage disorder, Niemann-Pick disease type C1. Here, we investigated acetyl-DL-leucine and its enantiomers acetyl-L-leucine and acetyl-D-leucine in symptomatic Npc1-/- mice and observed improvement in ataxia with both individual enantiomers and acetyl-DL-leucine. When acetyl-DL-leucine and acetyl-L-leucine were administered pre-symptomatically to Npc1-/- mice, both treatments delayed disease progression and extended life span, whereas acetyl-D-leucine did not. These data are consistent with acetyl-L-leucine being the neuroprotective enantiomer. Altered glucose and antioxidant metabolism were implicated as one of the potential mechanisms of action of the L enantiomer in Npc1-/- mice. When the standard of care drug miglustat and acetyl-DL-leucine were used in combination significant synergy resulted. In agreement with these pre-clinical data, when Niemann-Pick disease type C1 patients were evaluated after 12 months of acetyl-DL-leucine treatment, rates of disease progression were slowed, with stabilisation or improvement in multiple neurological domains. A beneficial effect of acetyl-DL-leucine on gait was also observed in this study in a mouse model of GM2 gangliosidosis (Sandhoff disease) and in Tay-Sachs and Sandhoff disease patients in individual cases of off-label-use. Taken together, we have identified an unanticipated neuroprotective effect of acetyl-L-leucine and underlying mechanisms of action in lysosomal storage diseases, supporting its further evaluation in clinical trials in lysosomal disorders."

For more on lysosomes:
https://www.lifeexte...autophagy-renew
"We know that recycling is good for the environment. But as it turns out, it’s also good for our cells: autophagy is a natural process by which cells clean up intra-cellular debris and other metabolic waste. Tiny cellular organelles called lysosomes breakdown and repurpose this spent material. So why does cellular autophagy matter? Because it helps our bodies conserve energy and function properly, which is essential to living a long, healthy life."

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#3 wholoman

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Posted 26 January 2021 - 11:49 AM

Found in online pharmacies under name of Tanganil.



#4 Believer

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Posted 29 January 2021 - 03:51 PM

What are their pharmacology since they help these diseases? Is it only MTOR activation?



#5 BrandonFlorida

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Posted 03 February 2021 - 03:29 AM

I don't know the answer to the specific question you asked, but I do know that it cannot stave off posterior vitreous detachments which everyone will experience with age.



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#6 Believer

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Posted 03 February 2021 - 05:01 PM

Do you think this would be better for MTOR activation for age related muscle loss and weakness than HMB or l-leucine alone?






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