Talk:Hormesis: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>Anthony.Sebastian
(New page: {{subpages}} ==Starting article on "hormesis"== Encouraging collaboration.)
 
imported>Howard C. Berkowitz
Line 2: Line 2:
==Starting article on "hormesis"==
==Starting article on "hormesis"==
Encouraging collaboration.
Encouraging collaboration.
== Hoping this is a reasonable approach ==
One of the first thing that hormesis brings to mind is type-0 and type-1 pharmacokinetics, especially drug (or toxin) clearance. Obviously simplified, zero-order kinetics has a basic model that the excretion process has infinite capacity, while first-order kinetics has a saturation point.
Such effects are at the high-end range of dose-effect mechanisms.
At a low end -- thinking of infection rather than drugs -- in biohazard mitigation and biological warfare work, there is a well-established "minimum infective concentration" (often expressed as the 50th percentile). [[Tularemia]], for example, can establish disease with only a few cells, where more dangerous agents require a considerably larger concenntration.
[[User:Howard C. Berkowitz|Howard C. Berkowitz]] 12:32, 1 October 2008 (CDT)

Revision as of 12:32, 1 October 2008

This article is developing and not approved.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
To learn how to update the categories for this article, see here. To update categories, edit the metadata template.
 Definition A quantitative and qualitative dose-response relationship in which the effect at low concentrations occurs in the opposite direction from that expected from the effect observed at higher concentrations. [d] [e]
Checklist and Archives
 Workgroup categories Health Sciences, Biology and Chemistry [Categories OK]
 Talk Archive none  English language variant American English

Starting article on "hormesis"

Encouraging collaboration.

Hoping this is a reasonable approach

One of the first thing that hormesis brings to mind is type-0 and type-1 pharmacokinetics, especially drug (or toxin) clearance. Obviously simplified, zero-order kinetics has a basic model that the excretion process has infinite capacity, while first-order kinetics has a saturation point.

Such effects are at the high-end range of dose-effect mechanisms.

At a low end -- thinking of infection rather than drugs -- in biohazard mitigation and biological warfare work, there is a well-established "minimum infective concentration" (often expressed as the 50th percentile). Tularemia, for example, can establish disease with only a few cells, where more dangerous agents require a considerably larger concenntration.

Howard C. Berkowitz 12:32, 1 October 2008 (CDT)