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The A1 component then binds to the ribosome, disrupting protein synthesis. Stx-2 has been found to be about 400 times more toxic (as quantified by LD 50 in mice) than Stx-1. Gb3 is, for unknown reasons, present in greater amounts in renal epithelial tissues, to which the renal toxicity of Shiga toxin may be attributed.
Toxic units (TU) are used in the field of toxicology to quantify the interactions of toxicants in binary mixtures of chemicals. [1] A toxic unit for a given compound is based on the concentration at which there is a 50% effect (ex. EC50) for a certain biological endpoint.
2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is the reference chemical to which the toxicity of other dioxins and DLCs are compared. TCDD is the most toxic DLC known. TCDD is the most toxic DLC known. Other dioxins and DLCs are assigned a scaling factor, or TEF, in comparison to TCDD.
Saxitoxin (STX) is a potent neurotoxin and the best-known paralytic shellfish toxin. Ingestion of saxitoxin by humans, usually by consumption of shellfish contaminated by toxic algal blooms , is responsible for the illness known as paralytic shellfish poisoning (PSP).
Syntaxin-2, also known as epimorphin, is a protein that in humans is encoded by the STX2 gene. [5] [6] [7] The product of this gene belongs to the syntaxin/epimorphin family of proteins. The syntaxins are a large protein family implicated in the targeting and fusion of intracellular transport vesicles.
NOAA originally calculated ERL/ERMs using existing toxicity data compiled from completed toxicity assays with varying endpoints, including effects on commonly tested organisms, particularly at sensitive life stages. The process is considered a "weight of evidence approach", in which results are based on a large database of previously conducted ...
Additionally, chronic toxicity tests tend to require significantly more attention and resources than acute tests which makes them much less feasible for basing decisions off of in a timely manner. The need for development of more advanced statistical methods, and uniformity in using these methods by regulators has been made apparent in literature.
The TLV is an estimate based on the known toxicity in humans or animals of a given chemical substance, and the reliability and accuracy of the latest sampling and analytical methods. TLVs do not take into account financial or technical feasibility for application in the workplace, instead solely focusing on health based recommendations to ...