2019
DOI: 10.3382/ps/pez197
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Saikosaponin A protects chickens against pullorum disease via modulation of cholesterol

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Cited by 11 publications
(10 citation statements)
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“…Medicinal plants are an important source for the discovery of potential new agents to control pathogens (Shuai-Cheng et al, 2019). In the present study, we found that glabrol, licochalcone A, licochalcone C, and licochalcone E displayed high efficiency against S. aureus , with low cell cytotoxicity to mammalian cells.…”
Section: Discussionmentioning
confidence: 99%
“…Medicinal plants are an important source for the discovery of potential new agents to control pathogens (Shuai-Cheng et al, 2019). In the present study, we found that glabrol, licochalcone A, licochalcone C, and licochalcone E displayed high efficiency against S. aureus , with low cell cytotoxicity to mammalian cells.…”
Section: Discussionmentioning
confidence: 99%
“…Because plants and microorganisms naturally produce a wide diversity of secondary metabolites that serve as defense compounds against pathogens, they are important sources for the discovery of natural products that interfere with bacterial virulence via different mechanisms of action . Indeed, many medicinal plants and probiotics have been widely used as complementary and alternative drugs for the treatment of infectious diseases …”
Section: Introductionmentioning
confidence: 99%
“…22 Indeed, many medicinal plants and probiotics have been widely used as complementary and alternative drugs for the treatment of infectious diseases. 23 Here, we provide a brief overview of the major virulence factors invoked by S. aureus to evade the host immune response or antibiotics as well as antivirulence compounds from plants and microorganisms for guiding the discovery and development of novel antibacterial drugs. We also outline the potential adjuvant effects of antivirulence strategy on existing antibiotics to overcome the antibiotic resistance of S. aureus.…”
Section: Introductionmentioning
confidence: 99%
“…Several sterane derivatives were demonstrated to target LXR-α and LXR-β activation 253 , 307 , 310 , 353 and/or LXRa/Lxra and LXRB/Lxrb upregulation, 330 , 332 , 354 , 355 , 356 , 357 resulting in induction of ABCA1 / Abca1 . Celastrol, 330 , 332 digoxin, 253 fucosterol, 308 certain gypenosides, 354 ouabain, 253 platycodin D, 355 saikosaponin A, 356 24-( S )-saringosterol, 307 24-( S )-stigmast-5-ene-3β,24-diol, 307 taxarasterol, 353 testosterone, 357 and TR1 310 increased ABCA1 / Abca1 mRNA 307 , 308 , 310 , 330 , 332 , 353 , 354 , 356 , 357 and/or ABCA1 protein content 310 , 253 , 353 , 354 , 355 , 357 leading to an enhanced efflux of cholesterol in vitro 253 , 308 , 330 , 332 and decreased intracellular cholesterol and/or phospholipid levels in vitro 330 , 332 , 354 , 356 , 357 and in vivo in mice. 253 The effect of fucosterol was comparable to that of the standard ABCA1 / Abca1 inducer TO901317.…”
Section: Part I: Status Quomentioning
confidence: 99%