Accordingly, an increased release of oxytocin causes certain cells in the heart wall to convert back into stem cells. These immature progenitor cells can then form new heart muscle cells and thus help to repair damaged parts of the heart – this could provide new approaches for regeneration after a heart attack.
Unlike other muscles, our heart muscle has only limited self-healing powers. If it is damaged by a heart attack or an injury, it is difficult to heal and heart failure often remains. One of the reasons for this is that there are hardly any stem cells in the heart from which new cardiomyocytes could form. However, there are initial indications that cells from the heart wall, the epicardium, can revert to stem cells under certain conditions – and then form new heart muscle cells.
Aaron Wasserman and his colleagues from Michigan State University have now discovered a decisive factor for this regeneration: the hormone oxytocin. The impetus for their study came from the observation that, unlike humans, zebrafish have no problem with heart regeneration: If their heart is injured, the heart muscle and its blood vessels quickly grow back. It does this by mass conversion of cells from the heart wall into epicardial-derived progenitor cells (EpiPC).
When the researchers were looking for the impetus for this transformation, they discovered something surprising in the brain of the zebrafish: Large amounts of the “cuddle hormone” oxytocin were released there in response to the heart injury. As a result, the messenger RNA for the production of this hormone increased 20-fold in the zebrafish brain in a short time. However, the hormone did not stay in the brain: It traveled with the blood to the heart, where it triggered a molecular cascade that initiated the conversion of the epicardial cells into the stem cells.
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This raises the question of whether this mechanism could also work in humans. Although a heart attack or heart injury does not trigger such an oxytocin surge in us, it is conceivable that the molecular reactions to the cuddle hormone are still present in us. To test this, Wassermann and his team cultured human heart wall cells and exposed them to oxytocin and, for comparison, 14 other neurotransmitters.
The surprising result: the human heart cells also reacted to the cuddle hormone. While the other messenger substances had little effect, under the influence of oxytocin they increasingly transformed into epicardium-derived progenitor cells. More detailed analyzes showed that these cells have their own oxytocin receptors for this, to which the cuddle hormone docks and thus initiates the conversion.
“We have thus shown that oxytocin can activate heart repair mechanisms in zebrafish and in human cell cultures,” says senior author Aitor Aguirre. “Apparently, this reaction to the oxytocin stimulation has also been preserved to a certain extent in human heart cells.” This could create new possibilities for promoting the regeneration of the heart after a heart attack or an injury in humans – for example by administering additional oxytocin becomes.
“Oxytocin has been used in medicine for other reasons for some time,” explains Aguirre. “It is therefore by no means utopian to use it in patients who have had a heart attack. Even if this only led to a partial regeneration of the heart, the benefits for the patients would be enormous.” Until then, however, the biochemical mechanism and the possible therapy have to be investigated in mammals in more detail. (Frontiers in Cell and Developmental Biology, 2022; doi:10.3389/fcell.2022.985298)
What: Frontiers
This article was written by Nadja Podbregar
The original to this post “Cuddle hormone” oxytocin can repair the heart” comes from scinexx.
