Uploaded July 2021 | Updated September 2026, 1 week ago
SPONSOR - Longevity.Technology - https://www.longevity.technology/?utm_source=youtube&utm_medium=social&utm_campaign=SSSheartshock
The heat shock response is an evolutionarily conserved response that causes the upregulation of many "molecular chaperones" within a cell. These "molecular chaperones", otherwise referred to as Heat shock proteins (Hsps), help unfolded proteins to re-fold, aid the assembly of protein complexes and help traffic proteins around a cell.
Although the response is named after its discovery in response to a heat-shock, the response is also activated in response to oxidative stress, viral invasion and glucose deprivation, all forms of cellular stress. The activation of heat shock proteins in times of cellular stress is therefore thought to be adaptive since it enables protein folding to be retained in detrimental conditions. A key mediator behind this response is HSF-1. Adding or removing copies of the gene encoding HSF1 in different model organisms has been shown to extend or reduce their lifespan, respectively. The maintenance of proteostasis within a cell is one of the hallmarks of aging and thus many studies reinforce the point that maintenance of a robust heat shock response is important for health and survival.
So, can activating the heat shock response be beneficial for healthspan? Well many molecules that can activate HSF1 have been identified and inhibitors of Hsp90 turn out to have senolytic activity. We will discuss this more in the video.
TIMESTAMPS
Intro - 00:00
Biochemistry of the heat shock response - 00:42
Heat shock proteins & aging - 04:45
Activating the heat shock response - 06:55
Senolytics - 08:20
REFERENCES
Ritossa, F. A new puffing pattern induced by temperature shock and DNP in drosophila. Experientia 18, 571–573 (1962). doi.org/10.1007/BF02172188
Regulation of Aging and Age-Related Disease by DAF-16 and Heat-Shock Factor - doi.org/10.1126/science.1083701
Regulation of Hsf1 Function in the Heat Stress Response: Implications in Aging and Disease - doi.org/10.1146/annurev-biochem-060809-095203
Regulation of the mammalian heat shock factor 1 - doi.org/10.1111/febs.13999
Hsps and aging - doi.org/10.1016/j.tem.2008.12.005
Fuhrmann-Stroissnigg, H., Ling, Y.Y., Zhao, J. et al. Identification of HSP90 inhibitors as a novel class of senolytics. Nat Commun 8, 422 (2017). doi.org/10.1038/s41467-017-00314-z
Check out @LongevityScienceNews 's videos !
Icons in intro; "freepik.com/free-photos-vectors/background"Background vector created by freepik - freepik.com
SPONSOR - Longevity.Technology - https://www.longevity.technology/?utm_source=youtube&utm_medium=social&utm_campaign=SSSheartshock
The heat shock response is an evolutionarily conserved response that causes the upregulation of many "molecular chaperones" within a cell. These "molecular chaperones", otherwise referred to as Heat shock proteins (Hsps), help unfolded proteins to re-fold, aid the assembly of protein complexes and help traffic proteins around a cell.
Although the response is named after its discovery in response to a heat-shock, the response is also activated in response to oxidative stress, viral invasion and glucose deprivation, all forms of cellular stress. The activation of heat shock proteins in times of cellular stress is therefore thought to be adaptive since it enables protein folding to be retained in detrimental conditions. A key mediator behind this response is HSF-1. Adding or removing copies of the gene encoding HSF1 in different model organisms has been shown to extend or reduce their lifespan, respectively. The maintenance of proteostasis within a cell is one of the hallmarks of aging and thus many studies reinforce the point that maintenance of a robust heat shock response is important for health and survival.
So, can activating the heat shock response be beneficial for healthspan? Well many molecules that can activate HSF1 have been identified and inhibitors of Hsp90 turn out to have senolytic activity. We will discuss this more in the video.
TIMESTAMPS
Intro - 00:00
Biochemistry of the heat shock response - 00:42
Heat shock proteins & aging - 04:45
Activating the heat shock response - 06:55
Senolytics - 08:20
REFERENCES
Ritossa, F. A new puffing pattern induced by temperature shock and DNP in drosophila. Experientia 18, 571–573 (1962). doi.org/10.1007/BF02172188
Regulation of Aging and Age-Related Disease by DAF-16 and Heat-Shock Factor - doi.org/10.1126/science.1083701
Regulation of Hsf1 Function in the Heat Stress Response: Implications in Aging and Disease - doi.org/10.1146/annurev-biochem-060809-095203
Regulation of the mammalian heat shock factor 1 - doi.org/10.1111/febs.13999
Hsps and aging - doi.org/10.1016/j.tem.2008.12.005
Fuhrmann-Stroissnigg, H., Ling, Y.Y., Zhao, J. et al. Identification of HSP90 inhibitors as a novel class of senolytics. Nat Commun 8, 422 (2017). doi.org/10.1038/s41467-017-00314-z
Check out @LongevityScienceNews 's videos !
Icons in intro; "freepik.com/free-photos-vectors/background"Background vector created by freepik - freepik.com





![The potential of fasting to delay aging (Periodic vs. intermittent)
In this video I discuss different types of fasting diets (both periodic and intermittent) and the underlying molecular mechanisms and why they have potential to delay aging and aging-related diseases. In particular we will address the importance of refeeding, which is more intense in periodic fasting (and fast mimicking diets [FMD]) due to the more severe fasting length, and activation of stem cells for regeneration & rejuvenation of tissues. We will also discuss the pros and concerns for fasting and how fasting overlaps or doesnt overlap with anti-aging supplements.
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TIMESTAMPS;
Intro - 0:00
Fasting diets - 01:10
Fasting mechanisms - 03:10
Longevity signalling - 04:30
Intermittent fasting pros & cons - 06:55
Periodic fasting - 10:15
Refeeding importance - 11:50
Supplements & fasting - 13:30
Which is better IF vs. PF? - 14:40
Other questions - 15:25
References;
Longo, V.D., Di Tano, M., Mattson, M.P. et al. Intermittent and periodic fasting, longevity and disease. Nat Aging 1, 47–59 (2021). https://doi.org/10.1038/s43587-020-00013-3
Panda & Longo review article - https://doi.org/10.1016/j.cmet.2016.06.001
TRF study - https://doi.org/10.1016/j.cmet.2012.04.019
FMD study - https://doi.org/10.1016/j.cmet.2015.05.012
Icons in intro; https://www.freepik.com/free-photos-vectors/backgroundBackground vector created by freepik - www.freepik.com The potential of fasting to delay aging (Periodic vs. intermittent)](https://i.ytimg.com/vi/y4CRQTpDJI0/mqdefault.jpg)




