Search results
Results From The WOW.Com Content Network
The dose–response relationship, or exposure–response relationship, describes the magnitude of the response of an organism, as a function of exposure (or doses) to a stimulus or stressor (usually a chemical) after a certain exposure time. [1] Dose–response relationships can be described by dose–response curves. This is explained further ...
For instance, if we assign dose concentration the symbol C, and time the classic t, then for any two dose schema, if C 1 t 1 =C 2 t 2, then under Haber's rule the two dose schema are equivalent. Haber's rule is an approximation, useful with certain inhaled poisons under certain conditions, and Haber himself acknowledged that it was not always ...
The fraction of bound receptors is known as occupancy. The relationship between occupancy and pharmacological response is usually non-linear. This explains the so-called receptor reserve phenomenon i.e. the concentration producing 50% occupancy is typically higher than the concentration producing 50% of maximum response. More precisely ...
Threshold dose is a dose of drug barely adequate to produce a biological effect in an animal. In dose-response assessment, the term ‘threshold dose’ is refined into several terminologies, such as NOEL, NOAEL, and LOAEL. They define the limits of doses resulting in biological responses or toxic effects. [3]
Toxciant concentration is on the X-axis and biological response is on the Y-axis. Point estimation is a technique to predict population parameters based on available sample data and can be used to relate the mass based concentration to a toxicity based metric. Point estimates in toxicology are frequently response endpoints on a dose response curve.
The threshold dose-response model is widely viewed as the most dominant model in toxicology. [ 6 ] An alternative type of model in toxicology is the linear no-threshold model (LNT), while hormesis correspond to the existence of opposite effects at low vs. high dose, which usually gives a U- or inverted U-shaped dose response curve.
In the context of toxicology, the hormesis model of dose response is vigorously debated. [8] The biochemical mechanisms by which hormesis works (particularly in applied cases pertaining to behavior and toxins) remain under early laboratory research and are not well understood. [6]
In toxicology it is specifically the highest tested dose or concentration of a substance (i.e. a drug or chemical) or agent (e.g. radiation), at which no such adverse effect is found in exposed test organisms where higher doses or concentrations resulted in an adverse effect. [3] [4] [5]