Icaritin protects against oxidative stress-induced injury in cardiac H9c2 cells via Akt/Nrf2/HO-1 and calcium signalling pathways
Icaritin, a prenylflavonoid isolated from Herbal Epimedii, is well known for its osteoplastic and anti-tumour activities. Here, we examined the cardioprotective actions of icaritin on cardiac H9c2 cells under oxidative stress conditions induced by treatment with tert-butylhydroperoxide (t-BHP). Icaritin at a concentration range between 1 and 4 µM effectively increased cell viability and decreased lactate dehydrogenase (LDH) leakage and reactive oxygen species (ROS) release in t-BHP treated cells, reflecting its ability to reduce t-BHP-induced cell injury. Icaritin also protected cell membrane integrity by preventing the collapse of the mitochondrial membrane potential. In addition, pretreatment of NF-E2-related factor 2 (Nrf2) siRNA and Akt inhibitor abolished the cardioprotective effect of icaritin. Furthermore, Nrf2 siRNA transfection interfered with the effect of icaritin on the inhibition of Ca2+ overload, whereas Akt inhibitor reduced icaritin-induced haemo-oxygenase-1 (HO-1) expression. Collectively, these results suggest that icaritin exerted its cardioprotective effect through the Akt/Nrf2/HO-1 and calcium signalling pathways..
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2015 |
---|---|
Erschienen: |
2015 |
Enthalten in: |
Zur Gesamtaufnahme - volume:18 |
---|---|
Enthalten in: |
Journal of Functional Foods - 18(2015), Seite 213-223 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Si Wan Lei [VerfasserIn] |
---|
Links: |
doi.org [kostenfrei] |
---|
Themen: |
Calcium ion |
---|
doi: |
10.1016/j.jff.2015.06.054 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
DOAJ054969689 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | DOAJ054969689 | ||
003 | DE-627 | ||
005 | 20230502075032.0 | ||
007 | cr uuu---uuuuu | ||
008 | 230227s2015 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.jff.2015.06.054 |2 doi | |
035 | |a (DE-627)DOAJ054969689 | ||
035 | |a (DE-599)DOAJ7aa3846b2bf94c53b93d763d75fa7e49 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
050 | 0 | |a TX341-641 | |
100 | 0 | |a Si Wan Lei |e verfasserin |4 aut | |
245 | 1 | 0 | |a Icaritin protects against oxidative stress-induced injury in cardiac H9c2 cells via Akt/Nrf2/HO-1 and calcium signalling pathways |
264 | 1 | |c 2015 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a Computermedien |b c |2 rdamedia | ||
338 | |a Online-Ressource |b cr |2 rdacarrier | ||
520 | |a Icaritin, a prenylflavonoid isolated from Herbal Epimedii, is well known for its osteoplastic and anti-tumour activities. Here, we examined the cardioprotective actions of icaritin on cardiac H9c2 cells under oxidative stress conditions induced by treatment with tert-butylhydroperoxide (t-BHP). Icaritin at a concentration range between 1 and 4 µM effectively increased cell viability and decreased lactate dehydrogenase (LDH) leakage and reactive oxygen species (ROS) release in t-BHP treated cells, reflecting its ability to reduce t-BHP-induced cell injury. Icaritin also protected cell membrane integrity by preventing the collapse of the mitochondrial membrane potential. In addition, pretreatment of NF-E2-related factor 2 (Nrf2) siRNA and Akt inhibitor abolished the cardioprotective effect of icaritin. Furthermore, Nrf2 siRNA transfection interfered with the effect of icaritin on the inhibition of Ca2+ overload, whereas Akt inhibitor reduced icaritin-induced haemo-oxygenase-1 (HO-1) expression. Collectively, these results suggest that icaritin exerted its cardioprotective effect through the Akt/Nrf2/HO-1 and calcium signalling pathways. | ||
650 | 4 | |a Icaritin | |
650 | 4 | |a Cardiac H9c2 cells | |
650 | 4 | |a Oxidative stress | |
650 | 4 | |a NF-E2-related factor 2 | |
650 | 4 | |a Calcium ion | |
653 | 0 | |a Nutrition. Foods and food supply | |
700 | 0 | |a Guozhen Cui |e verfasserin |4 aut | |
700 | 0 | |a George Pak Heng Leung |e verfasserin |4 aut | |
700 | 0 | |a Sharon Chui Wah Luk |e verfasserin |4 aut | |
700 | 0 | |a Maggie Pui Man Hoi |e verfasserin |4 aut | |
700 | 0 | |a Liang Wang |e verfasserin |4 aut | |
700 | 0 | |a Gail B. Mahady |e verfasserin |4 aut | |
700 | 0 | |a Simon Ming Yuen Lee |e verfasserin |4 aut | |
773 | 0 | 8 | |i In |t Journal of Functional Foods |d Elsevier, 2021 |g 18(2015), Seite 213-223 |w (DE-627)DOAJ078609844 |x 22149414 |7 nnns |
773 | 1 | 8 | |g volume:18 |g year:2015 |g pages:213-223 |
856 | 4 | 0 | |u https://doi.org/10.1016/j.jff.2015.06.054 |z kostenfrei |
856 | 4 | 0 | |u https://doaj.org/article/7aa3846b2bf94c53b93d763d75fa7e49 |z kostenfrei |
856 | 4 | 0 | |u http://www.sciencedirect.com/science/article/pii/S1756464615003485 |z kostenfrei |
856 | 4 | 2 | |u https://doaj.org/toc/1756-4646 |y Journal toc |z kostenfrei |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_DOAJ | ||
912 | |a SSG-OLC-PHA | ||
951 | |a AR | ||
952 | |d 18 |j 2015 |h 213-223 |