Omaveloxolone ameliorates isoproterenol-induced pathological cardiac hypertrophy in mice DOI

Xianchao Li,

Yang Wu,

Yunzhao Yang

et al.

Free Radical Research, Journal Year: 2023, Volume and Issue: 58(1), P. 57 - 68

Published: Dec. 25, 2023

Nuclear factor erythroid 2-related 2 (Nrf2) is an important transcriptional regulator that plays a protective role against various cardiovascular diseases. Omaveloxolone newly discovered potent activator of Nrf2 has variety cytoprotective functions. However, the potential omaveloxolone in process pathological cardiac hypertrophy and heart failure are still unknown. In this study, isoproterenol (ISO)-induced model was established to investigate effect vivo vitro. Our study first confirmed administration improved ISO-induced mice neonatal cardiomyocytes. also diminished oxidative stress, inflammation cardiomyocyte apoptosis. addition, activated signaling pathway, knockdown almost completely abolished cardioprotective omaveloxolone, indicated directly related activation signaling. summary, our identified may be promising therapeutic agent mitigate hypertrophy.

Language: Английский

ACE2 activation alleviates sepsis-induced cardiomyopathy by promoting MasR-Sirt1-mediated mitochondrial biogenesis DOI

Tiantian Wan,

Ya Li, Jiaxin Li

et al.

Archives of Biochemistry and Biophysics, Journal Year: 2023, Volume and Issue: 752, P. 109855 - 109855

Published: Dec. 13, 2023

Language: Английский

Citations

5

Pleiotropic Effects of Peroxisome Proliferator-Activated Receptor Alpha and Gamma Agonists on Myocardial Damage: Molecular Mechanisms and Clinical Evidence—A Narrative Review DOI Creative Commons
María Esther Rubio-Ruíz, Juan Carlos Plata-Corona, Elizabeth Soria‐Castro

et al.

Cells, Journal Year: 2024, Volume and Issue: 13(17), P. 1488 - 1488

Published: Sept. 5, 2024

Cardiovascular diseases remain the leading cause of death in world, and that is why finding an effective multi-functional treatment alternative to combat these has become more important. Fibrates thiazolidinediones, peroxisome proliferator-activated receptors alpha gamma are pharmacological therapies used treat dyslipidemia type 2 diabetes, respectively. New mechanisms action drugs have been found, demonstrating their pleiotropic effects, which contribute preserving heart by reducing or even preventing myocardial damage. Here, we review underlying cardioprotective effects PPAR agonists regulating morphological physiological alterations (metabolic flexibility, mitochondrial damage, apoptosis, structural remodeling, inflammation). Moreover, clinical evidence regarding effect also addressed.

Language: Английский

Citations

1

Investigating the potential neuroprotective benefits of taurine and Dihydrotestosterone and Hydroxyprogesterone levels in SH-SY5Y cells DOI Creative Commons
Hailah M. Almohaimeed, Amany I. Almars,

Fayez Alsulaimani

et al.

Frontiers in Aging Neuroscience, Journal Year: 2024, Volume and Issue: 16

Published: May 29, 2024

Background Taurine, an amino acid abundantly found in the brain and other tissues, has potential neuroprotective properties. Alzheimer’s disease (AD) is a commonly occurring type of dementia, which becomes more prevalent as people age. This experiment aimed to assess effects taurine on SH-SY5Y cells by examining its impact Dihydrotestosterone (DHT), Dihydroprogesterone (DHP), well expression miRNA-21 miRNA-181. Methods The various concentrations (0.25, 0.75 mg/mL), LPS (0.1, 12 mg/mL) cell line were assessed using MTT assay. levels DHT DHP quantified ELISA kit. Additionally, miRNA-181 genes examined through Real-Time PCR analysis. Results results assay showed that treatment with at 0.25, mg/mL reduces toxicity cells. indicated concentration significantly elevated hormones compared untreated group ( p < 0.01). IL-1β IL-6 decreased under influence after (p Gene analysis revealed increasing resulted heightened miRNA-21, most significant increase observed 0.001). Conclusion Our study findings can be enhanced taurine. Consequently, exploring targeting taurine, miRNA-181, or considering hormone therapy may offer therapeutic approaches for treating AD alleviating severe symptoms. Nonetheless, order fully comprehend precise mechanisms involved, additional research required.

Language: Английский

Citations

0

SIRT1 activation promotes energy homeostasis and reprograms liver cancer metabolism DOI Creative Commons

Benluvankar Varghese,

Ugo Chianese, Lucia Capasso

et al.

Research Square (Research Square), Journal Year: 2023, Volume and Issue: unknown

Published: July 12, 2023

Abstract Background Cancer cells are characterized by uncontrolled cell proliferation and impaired bioenergetics. Sirtuins a family of highly conserved enzymes that play fundamental role in energy metabolism regulation. SIRT1, particular, drives many physiological stress responses metabolic pathways following nutrient deprivation. We previously showed SIRT1 activation using SCIC2.1 was able to attenuate genotoxic response senescence. Here, we report hepatocellular carcinoma (HCC) under glucose-deprived conditions, treatment induced overexpression SIRT3, SIRT6, modulating response. Methods Flow cytometry used analyze the cycle. The MTT assay xCELLigence system were measure viability proliferation. In vitro enzymatic assays carried out as directed manufacturer, absorbance measured with an automated Infinite M1000 reader. Western blotting immunoprecipitation evaluate expression various proteins described this study. relative genes studied real-time PCR. employed Seahorse XF24 Analyzer determine state cells. Oil Red O staining lipid accumulation. Results significantly promoted mitochondrial biogenesis via AMPK-p53-PGC1α pathway enhanced ATP production glucose inhibition EX-527 further supported our hypothesis effects dependent on activation. Interestingly, reprogrammed fatty acid oxidation for bioenergetic circuits repressing de novo lipogenesis. addition, SCIC2.1-mediated strongly modulated antioxidant through SIRT3 activation, p53-dependent indirect recruitment SIRT6. Conclusion Our results show is promote homeostasis, attenuating deprivation SIRT1. These findings shed light action pathogenesis HCC may help future therapies and, possibly, other diseases.

Language: Английский

Citations

1

Omaveloxolone ameliorates isoproterenol-induced pathological cardiac hypertrophy in mice DOI

Xianchao Li,

Yang Wu,

Yunzhao Yang

et al.

Free Radical Research, Journal Year: 2023, Volume and Issue: 58(1), P. 57 - 68

Published: Dec. 25, 2023

Nuclear factor erythroid 2-related 2 (Nrf2) is an important transcriptional regulator that plays a protective role against various cardiovascular diseases. Omaveloxolone newly discovered potent activator of Nrf2 has variety cytoprotective functions. However, the potential omaveloxolone in process pathological cardiac hypertrophy and heart failure are still unknown. In this study, isoproterenol (ISO)-induced model was established to investigate effect vivo vitro. Our study first confirmed administration improved ISO-induced mice neonatal cardiomyocytes. also diminished oxidative stress, inflammation cardiomyocyte apoptosis. addition, activated signaling pathway, knockdown almost completely abolished cardioprotective omaveloxolone, indicated directly related activation signaling. summary, our identified may be promising therapeutic agent mitigate hypertrophy.

Language: Английский

Citations

1