Depression is a chronic mental disorder characterized by persistent low mood and loss of interest, often associated with dysregulation of neuroinflammatory pathways. Inhibition of NOD-like receptor protein 3 (NLRP3), a key mediator of neuroinflammation, is a promising strategy for alleviating depressive symptoms by modulating inflammatory responses in the brain. Seven polycyclic polyprenylated acylphloroglucinols (PPAPs), including six new hyperioxides A-F (1-6) and furohyperforin (7) were isolated from St. John's wort and characterized via spectroscopic analyses. Compounds 2 and 7 exhibited neuroprotective effects at 10 μM in corticosterone (CORT)-injured SH-SY5Y cells. Furthermore, furohyperforin (7) was demonstrated potent antidepressant activity at 1.25 mg/kg in the forced swimming test (FST) of mice, which was equivalent to fluoxetine (10 mg/kg) and neurostan (78 mg/kg). Additionally, compound 7 was shown to reduce serum CORT levels in mice. Further studies highlighted its effects and potential mechanism through the NLRP3 inflammasome pathway and NLRP3 might be a protein target for the antidepressant effects of 7. Notably, this study provided the first evidence of furohyperforin (7)'s antidepressant properties in mice, highlighting its potential as a bioactive compound for antidepression.
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http://dx.doi.org/10.1016/j.ijbiomac.2025.141721 | DOI Listing |
J Cell Mol Med
March 2025
Department of Cardiology, The Affiliated Hospital of Jiangnan University, Wuxi, Jiangsu, China.
Recent research has revealed a close association between obesity and various metabolic disorders, including renal metabolic diseases, but the mechanism is still unknown. This study explored the role of p16INK4a in obesity-related kidney fibrosis and evaluated its potential as a therapeutic target. Using wild-type (WT) mice and p16 KO mice, we fed both groups a high-fat diet (HFD) for 6 months.
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March 2025
People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Cardiovascular disease (CVD) continues to be the leading cause of mortality worldwide. The nucleotide oligomerization domain-, leucine-rich repeat-, and pyrin domain-containing protein 3 (NLRP3) inflammasome is involved in numerous types of CVD. As part of innate immunity, the NLRP3 inflammasome plays a vital role, requiring priming and activation signals to trigger inflammation.
View Article and Find Full Text PDFInt J Mol Sci
March 2025
College of Pharmaceutical Science, Yunnan University of Chinese Medicine, 1076 Yuhua Road, Kunming 650500, China.
Metabolic dysfunction-associated fatty liver disease (MAFLD) affects approximately one-quarter of the world's adult population, and no effective therapeutic drugs are available. is a fungus used as a herb and food nutrient for centuries as well as for MAFLD treatment. Exosome-like nanovesicles have many pharmacological activities; however, studies on the effects of -derived exosome-like nanovesicles (PCELNs) on MAFLD are lacking.
View Article and Find Full Text PDFInt J Mol Sci
March 2025
Laboratory of Health Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan.
I3MT-3 (HMPSNE) has been identified as a selective inhibitor of the supersulfide-producing enzyme 3-MST. In this study, we found that I3MT-3 inhibits inflammatory responses, including the secretion of the pro-inflammatory cytokine interleukin-1β (IL-1β) and inflammatory cell death pyroptosis, induced by the activation of the inflammasomes composed of NLRP1, NLRP3, or AIM2. However, interestingly, the knockdown of 3-MST did not affect the activation of the inflammasomes, suggesting that the inhibitory effect of I3MT-3 on inflammasome activation is mediated by alternative ways rather than the inhibition of 3-MST.
View Article and Find Full Text PDFInt J Mol Sci
February 2025
Division of Cardiology, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.
Proprotein convertase subtilisin/kexin type 9 (PCSK9) has emerged as a novel target for reducing low-density lipoprotein cholesterol. PCSK9 activates the atherosclerosis process through pro-inflammation signaling. Furthermore, the serum level of PCSK9 is positively correlated with mortality in patients with heart failure (HF).
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