Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Wednesday, January 4, 2023

Curcumin, a Dietary Natural Supplement, Prolongs the Action Potential Duration of KCNE1-D85N Induced Pluripotent Stem Cell-Derived Cardiomyocytes

Ask your doctor if this means you shouldn't be getting the benefits of tumeric and curcumin and what would replace those benefits.

 

Your doctor's responsibility to come up with a solution.

Curcumin, a Dietary Natural Supplement, Prolongs the Action Potential Duration of KCNE1-D85N Induced Pluripotent Stem Cell-Derived Cardiomyocytes

Published:December 27, 2022DOI:https://doi.org/10.1016/j.hrthm.2022.12.034

Abstract

BACKGROUND

Curcumin, a polyphenolic dietary natural compound and active ingredient in turmeric, exerts antioxidant, anti-inflammatory, antidiabetic, anti-cancer, and antiarrhythmic properties. KCNE1-D85N, present in approximately 1% of Caucasians, is a common, potentially pro-arrhythmic variant that predisposes individuals to drug-induced QT prolongation under certain conditions.

OBJECTIVE

To test the hypothesize that curcumin might cause action potential duration (APD) prolongation in KCNE1-D85N derived human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs).

METHODS

Gene-edited/variant-corrected isogenic control and patient-specific, KCNE1-D85N containing iPSC-CMs were generated previously. Fluovolt, multielectrode array (MEA), and whole-cell patch clamp were performed to measure APD without and with 4-hour incubation of 10 nM Curcumin.

RESULTS

KCNE1-D85N derived iPSC-CMs demonstrated significant APD prolongation with treatment of 10 nM curcumin. Using Fluovolt, the APD90 was 578 ± 7 ms (n=39) at baseline and was prolonged to 658 ± 13 ms (n=35, p<0.0001) with curcumin incubation. Using MEA, the APD90 at baseline was 237 ± 6 ms (n=24), compared to 280 ± 6 ms (n=12, p=0.0002) with curcumin incubation. Whole-cell patch clamp confirmed these results with the APD90 of 544 ± 37 ms at baseline and 664 ± 40 ms (p < 0.005) with treatment of curcumin. However, the APD from isogenic control iPSC-CMs remained unchanged with curcumin treatment.

CONCLUSIONS

This study provides pharmacological and functional evidence to suggest that curcumin, a dietary natural supplement, might cause APD prolongation in the patients with common, potentially pro-arrhythmic functional variants such as KCNE1-D85N. Whether this supplement is potentially dangerous for the Caucasian sub-population who possess this variant warrants further investigation.

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