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[[Information on nutritional supplements people with ALS have been taking]]
 
[[Information on nutritional supplements people with ALS have been taking]]
 
* [https://en.wikipedia.org/wiki/Peony Wikipedia page]
 
  
 
== Effects on ALS ==
 
== Effects on ALS ==
  
Potential HSP-70 inducer: ''Treatment of cells with paeoniflorin but not glycyrrhizin resulted in enhanced phosphorylation and acquisition of the deoxyribonucleic acid–binding ability of heat shock transcription factor 1 (HSF1), as well as the formation of characteristic HSF1 granules in the nucleus, suggesting that the induction of HSPs by paeoniflorin is mediated by the activation of HSF1.'' {{#pmid:15633296|yan2004}}
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Potential HSP-70 inducer: ''Treatment of cells with paeoniflorin but not glycyrrhizin resulted in enhanced phosphorylation and acquisition of the deoxyribonucleic acid–binding ability of heat shock transcription factor 1 (HSF1), as well as the formation of characteristic HSF1 granules in the nucleus, suggesting that the induction of HSPs by paeoniflorin is mediated by the activation of HSF1.'' [1]
  
''Furthermore, PF decreased the release of IL-1β, IL-6 and TNF-α as well as inhibited the mRNA expression of IL-1β, IL-6 and TNF-α in the hippocampus of VD rats (P<0.05 or P<0.01). PF also could decrease the protein expressions of inducible nitric oxide synthase and cyclooxygenase-2 in the hippocampus of VD rats (P<0.05 orP<0.01). In addition, PF significantly inhibited the nuclear factor κB (NF-κB) pathway in the hippocampus of VD rats.'' {{#pmid:26577108|yang2015}}
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== Discussion threads on the ALSTDI forum ==
  
''Here, we have examined the efficacy of PF in the repression of inflammation-induced neurotoxicity and microglial inflammatory response. In organotypic hippocampal slice cultures, PF significantly blocked lipopolysaccharide (LPS)-induced hippocampal cell death and productions of nitric oxide (NO) and interleukin (IL)-1β. PF also inhibited the LPS-stimulated productions of NO, tumor necrosis factor-α, and IL-1β from primary microglial cells. These results suggest that PF possesses neuroprotective activity by reducing the production of proinflammatory factors from activated microglial cells.'' {{#pmid:23559368|nam2013}}
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[http://www.alstdi.org/forum/yaf_postst48193_peony-root-and-paeoniflorin-long-essay.aspx Peony root and paeoniflorin - long essay]
  
'' We found that PF inhibited the expression of CD69/CD86 and the proliferation of B cells stimulated by LPS. In addition, PF reduced the B-cell differentiation and immunoglobulin production that was stimulated by LPS. Interestingly, PF did not alter B-cell activation and proliferation provoked by anti-CD40 or IL-4. These results indicated for the first time that PF inhibits B-cell activation, proliferation and differentiation by selectively blocking the LPS/TLR4 signaling pathway. Furthermore, our data suggest that PF selectively inhibits inflammation and tissue damage mediated by LPS-activated B cells but does not alter CD40/CD40L- or IL-4-provoked B-cell function in autoimmune diseases treatment, which might aid in protecting patients from secondary infection.'' {{#pmid:26041080|zhang2015}}
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[http://www.alstdi.org/forum/default.aspx?g=posts&t=45820 Heat shock inducers]
  
<a href=http://stromectol.one>medication ivermectin 3mg</a> Wu H H, Reindollar Richard H, Gray MR
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[http://www.alstdi.org/forum/yaf_postst53948_peony-root.aspx Peony root]
  
 
== References ==
 
== References ==
  
 
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[1]
[[Category:Supplement data pages]]
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<bibtex>
[[Category:Anti-inflammatory supplements]]
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@article{Yan2004,
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abstract = {Heat shock proteins (HSPs) are induced by various physical, chemical, and biological stresses. HSPs are known to function as molecular chaperones, and they not only regulate various processes of protein biogenesis but also function as lifeguards against proteotoxic stresses. Because it is very useful to discover nontoxic chaperone-inducing compounds, we searched for them in herbal medicines. Some herbal medicines had positive effects on the induction of HSPs (Hsp70, Hsp40, and Hsp27) in cultured mammalian cells. We next examined 2 major constituents of these herbal medicines, glycyrrhizin and paeoniflorin, with previously defined chemical structures. Glycyrrhizin had an enhancing effect on the HSP induction by heat shock but could not induce HSPs by itself. In contrast, paeoniflorin had not only an enhancing effect but also an inducing effect by itself on HSP expression. Thus, paeoniflorin might be termed a chaperone inducer and glycyrrhizin a chaperone coinducer. Treatment of cells with paeoniflorin but not glycyrrhizin resulted in enhanced phosphorylation and acquisition of the deoxyribonucleic acid-binding ability of heat shock transcription factor 1 (HSF1), as well as the formation of characteristic HSF1 granules in the nucleus, suggesting that the induction of HSPs by paeoniflorin is mediated by the activation of HSF1. Also, thermotolerance was induced by treatment with paeoniflorin but not glycyrrhizin. Paeoniflorin had no toxic effect at concentrations as high as 80 microg/ mL (166.4 microM). To our knowledge, this is the first report on the induction of HSPs by herbal medicines.},
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author = {Yan, Dai and Saito, Kiyoto and Ohmi, Yuri and Fujie, Noriyo and Ohtsuka, Kenzo},
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file = {:C$\backslash$:/Users/riku/AppData/Local/Mendeley Ltd./Mendeley Desktop/Downloaded/Yan et al. - 2004 - Paeoniflorin, a novel heat shock protein-inducing compound.pdf:pdf},
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issn = {1355-8145},
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journal = {Cell stress \& chaperones},
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keywords = {Animals,Anti-Infective Agents,Anti-Infective Agents: pharmacology,Benzoates,Benzoates: metabolism,Bridged Compounds,Bridged Compounds: metabolism,DNA-Binding Proteins,DNA-Binding Proteins: drug effects,DNA-Binding Proteins: metabolism,Electrophoretic Mobility Shift Assay,Glucosides,Glucosides: genetics,Glucosides: metabolism,Glycyrrhizic Acid,Glycyrrhizic Acid: pharmacology,HeLa Cells,Heat-Shock Proteins,Heat-Shock Proteins: drug effects,Heat-Shock Proteins: metabolism,Herbal Medicine,Hot Temperature,Humans,Monoterpenes,Paeonia,Paeonia: metabolism,Phytotherapy,Rats,Transcription Factors},
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mendeley-groups = {peony},
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month = jan,
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number = {4},
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pages = {378--89},
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pmid = {15633296},
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title = {{Paeoniflorin, a novel heat shock protein-inducing compound.}},
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url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1065277\&tool=pmcentrez\&rendertype=abstract},
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volume = {9},
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year = {2004}
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}
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</bibtex>

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