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| home:protocol:mp_antibiotics [08.23.2014] – deemphasized antibiotics paulalbert | home:protocol:mp_antibiotics [09.14.2022] (current) – external edit 127.0.0.1 | ||
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| ^Name | ^Name | ||
| |Minocycline | |Minocycline | ||
| - | |Azithromycin (Zithromax) //no longer recommended// | + | |Azithromycin (Zithromax) //no longer recommended// |
| |Clindamycin | |Clindamycin | ||
| |Demeclocycline (Declomycin) | |Demeclocycline (Declomycin) | ||
| Line 58: | Line 58: | ||
| The affinity (Kd) of minocycline for the bacteria' | The affinity (Kd) of minocycline for the bacteria' | ||
| - | A recent paper has suggested that various tetracycline antibiotics including clindamycin activate the PXR.(({{pubmed> | + | A recent paper has suggested that various tetracycline antibiotics including clindamycin activate the PXR.(({{pmid> |
| The conclusion of that paper is somewhat at odds with the //in silico// model produced by Trevor Marshall, PhD, from which he has concluded that of the tetracyclines, | The conclusion of that paper is somewhat at odds with the //in silico// model produced by Trevor Marshall, PhD, from which he has concluded that of the tetracyclines, | ||
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| ==== Inhibition of caspase-3 (minocycline) ==== | ==== Inhibition of caspase-3 (minocycline) ==== | ||
| - | Caspase-3 is a protease, which breaks apart the VDR receptor structure and thus limits the ability of VDR to do gene transcription. Minocycline is known to inhibit Caspase-3 activation.(({{pubmed> | + | Caspase-3 is a protease, which breaks apart the VDR receptor structure and thus limits the ability of VDR to do gene transcription. Minocycline is known to inhibit Caspase-3 activation.(({{pmid> |
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| --></ | --></ | ||
| + | < | ||
| ===== Notes and comments ===== | ===== Notes and comments ===== | ||
| - | ===== References ===== | + | ===== References =====</ |