Could selective mitochondrial Autophagy combined with mitochondrial biogenesis be used to develop a cure for Mitochondrial diseases?
that if there is a way to to make Parkin-Pink1 bind to the autophagy receptor without ROS inside the mutant mitochondria. i know ROS causes the Parkin-Pink1 to bind to the autophagy receptor of damaged mitochondria due to lots of ROS being produced from ATP synthesis as a sort of by product of ATP synthesis. are any super tiny ligands or artificial molecular ligands that could be be used to make Parkin-Pink1 bind to the autophagy receptors. And is there a difference between universal Autophagy receptors and selective autophagy？ i would really be interested in hearing what Dr. Dave Chan has to say about autophagy being used to develop a treatment for mitochondrial diseases.
If you really want to control cancer, heart disease or ANY chronic disease you must focus on ENDING your own cold, flu and 100+ so called common symptoms. It’s not complicated. It is about WHAT YOU EAT. Period.
This was great, I have been researching “mitochondrial function for kids” for a while now, and I think this has helped. Have you ever come across – Miyason Mitochondria Masker – (do a search on google ) ? Ive heard some interesting things about it and my neighbour got amazing results with it
Not sure if I understood correctly, but On the Smart Drug Smarts episode #226, Navdeep mentions there’s ~10 copies of the mitochondria dna inside a single mitochondria cell.. and, aside from red blood cells, there are anywhere between1500 to 100,000+ mitochondrial cells inside a single human cell (depending on the cell function), is that correct?
Also, not only do Mitochondrial mutations (PINK1, PARKIN, etc) lead to energy deficiencies that give rise to specific diseases (Parkinson’s, periodontal, etc).. but they also are responsible for aging symptoms in general, where the somatic mutations accumulate eventually damaging tissues. Interestingly, Aubrey de Grey suggests mitochondrial damage is not the single most dominant cause of senescence.
Is there anything to maximize mitochondria health and reduce excess ROS and/or promote proper autophagy? Infrared exposure? Vitamin K2? Elysium’s NAD+ product, Basis? Endurance vs intensity exercises? Keto diet? BaCopa, Phosphatidyslerine, Pycnogenol, CDP Choline, and BioPQQ / Sulbutiamine (synthetic version of Vitamin B1 Thiamine)?
There’s also a couple great resources.. ‘mRNA to protein’ on the Khan Academy channel.. Dr. Lee Know interview on the 40+ Fitness podcast… Radiolabs’ The Primordial Journey series, and finally Dr. Douglas Wallace on the recent Stem Talk podcast. In the latter, it’s mentioned that mitochondria started as proteobacteria that formed a symbiotic relationship with archaebacteria, deep in the ocean, transferring all but 37 of it’s 1500 genes over to the nucleus dna (1h7m18s)!
7:24 ~ #Mitochondria are the librarian, lawyers, paralegal research, of the Library Vault Archives Card Catalog inside most Cells.
Isn’t it funny how just right after all these scientists finds out that Metformin cures cancer, that Metformin gets recalled…. lol
Could selective mitochondrial Autophagy combined with mitochondrial biogenesis be used to develop a cure for Mitochondrial diseases?
that if there is a way to to make Parkin-Pink1 bind to the autophagy receptor without ROS inside the mutant mitochondria. i know ROS causes the Parkin-Pink1 to bind to the autophagy receptor of damaged mitochondria due to lots of ROS being produced from ATP synthesis as a sort of by product of ATP synthesis. are any super tiny ligands or artificial molecular ligands that could be be used to make Parkin-Pink1 bind to the autophagy receptors. And is there a difference between universal Autophagy receptors and selective autophagy？ i would really be interested in hearing what Dr. Dave Chan has to say about autophagy being used to develop a treatment for mitochondrial diseases.
Strengthen Your Mitochondrial Function https://inurl.io/cellstrengthshot
Voice keeps fluctuating
If you really want to control cancer, heart disease or ANY chronic disease you must focus on ENDING your own cold, flu and 100+ so called common symptoms. It’s not complicated. It is about WHAT YOU EAT. Period.
This was great, I have been researching “mitochondrial function for kids” for a while now, and I think this has helped. Have you ever come across – Miyason Mitochondria Masker – (do a search on google ) ? Ive heard some interesting things about it and my neighbour got amazing results with it
Not sure if I understood correctly, but On the Smart Drug Smarts episode #226, Navdeep mentions there’s ~10 copies of the mitochondria dna inside a single mitochondria cell.. and, aside from red blood cells, there are anywhere between1500 to 100,000+ mitochondrial cells inside a single human cell (depending on the cell function), is that correct?
Also, not only do Mitochondrial mutations (PINK1, PARKIN, etc) lead to energy deficiencies that give rise to specific diseases (Parkinson’s, periodontal, etc).. but they also are responsible for aging symptoms in general, where the somatic mutations accumulate eventually damaging tissues. Interestingly, Aubrey de Grey suggests mitochondrial damage is not the single most dominant cause of senescence.
Is there anything to maximize mitochondria health and reduce excess ROS and/or promote proper autophagy? Infrared exposure? Vitamin K2? Elysium’s NAD+ product, Basis? Endurance vs intensity exercises? Keto diet? BaCopa, Phosphatidyslerine, Pycnogenol, CDP Choline, and BioPQQ / Sulbutiamine (synthetic version of Vitamin B1 Thiamine)?
There’s also a couple great resources.. ‘mRNA to protein’ on the Khan Academy channel.. Dr. Lee Know interview on the 40+ Fitness podcast… Radiolabs’ The Primordial Journey series, and finally Dr. Douglas Wallace on the recent Stem Talk podcast. In the latter, it’s mentioned that mitochondria started as proteobacteria that formed a symbiotic relationship with archaebacteria, deep in the ocean, transferring all but 37 of it’s 1500 genes over to the nucleus dna (1h7m18s)!
Mitochondrial cannabinoid receptor one regulates complex 1 activity
Allows for adequate atp while down regulating (excess) mitoROS production
🙂 happy to be first