Jump to content
RemedySpot.com

T-2 toxin and Satratoxin

Rate this topic


Guest guest

Recommended Posts

http://www.cbwinfo.com/Biological/Toxins/T2.html

T-2 Toxin:

essential data

Symptoms, Treatment, Decontamination

Syndrome Name none

Symptoms

* skin irritation

* loss of function in:

o intestines,

o bone marrow,

o lymph nodes,

o spleen

o thymus

* Alimentary Toxic Aleukia (time course: 8 weeks with rapid onset

of symptoms)

* burning sensation in alimentary tract

* vomiting

* tachycardia

* leukopenia

* petechial hemorrhages with necrosis in skin

* internal hemorrhages

Onset of Symptoms

There is a fairly quick (<20 minutes) response similar to that seen

with mustard (blistering of the skin and irritation of the eyes and

throat). Symptoms of systemic poisoning appear relatively slowly

(>8-12 hours.)

Rapid diagnostic assay

None, but rapid and sensitive assays for the detection and monitoring

of trichothecenes in cereals are available. They may not be readily

adaptable to human diagnostics.

Antidote

None

Supportive Care

Removal of ingested toxins by treatment with adsorbents such as

superactivated charcoal; treatment of symptoms

Inactivation

Decontamination with soap and water.

Return to Top

Toxicology of T-2

LD50's by Route of Administration

Test

Organism Inhalation Intravenous Subcutaneous Dermal

Mouse 0.24-0.94 mg/kg 3.8 mg/kg 1.6-2.1 mg/kg >10 mg/kg

Guinea pig 5749 mg.min.m-3

Rat 2000 mg.min.m-3

Pig <2.7 mg/kg 1.2 mg/kg

Return to Top

Chemical Properties

Structure

CA Name Trichothec-9-ene-3,4,8,15-tetrol,12,13-epoxy-, 4,15-diacetate

8-(3-methylbutanoate), (3.alpha.,4.beta.,8.alpha.)-

Trivial Names

* Fusariotoxin T 2

* Insariotoxin

* Mycotoxin T 2

* NSC 138780

* T 2

* T 2 mycotoxin

Registry Number 21259-20-1

RTECS Number YD0100000

Molecular

Formula C24 H34 O9

Molecular

weight 466.57

Solubility Insoluble in water,

soluble in lower alcohols and polar solvents including

* methanol,

* ethanol,

* isopropanol

* propylene glycol,

* acetone,

* ethyl acetate

* chloroform,

* dimethyl sulfoxide

pKa in water Not applicable

Complete synthesis None

Return to Top

Site of Action

T-2 and most of the other trichothecene mycotoxins considered for use

as weapons act by inhibiting protein synthesis. They do this by

reacting with components of the ribosomes: the structure within the

cell where proteins are made. The specific site of action of T-2,

which is a reaction with a critical site on the ribosomal RNA (rRNA)

is known.

Protein synthesis is an essential function in all tissues, but tissues

where cells are actively and rapidly growing and dividing are very

susceptible to the toxins. Susceptible tissues therefore include:

the lining of the digestive tract, the wear and tear of the digestive

process is constantly being repaired;

bone marrow, the site of the continuous formation of new red and white

blood cells;

the lymph nodes, a key site in the immune system;

the spleen, also a vital component of the immune system

the liver, metabolically the most active tissue of the body.

Tissues like the brain and muscle are less severely affected.

Source

Several species of the genus Fusarium synthesize the toxin. A

definitive list is hard to construct because of the problems of

identification of species within the genus.

Fermentation of T-2 toxin can be very efficient with yields of several

grams of the toxin for every kilogram of substrate, even using

relatively inefficient culture on a solid medium rather than liquid

fermentation.

Agent Properties

Trichothecenes are different from most other potential weapons toxins

because they can act through the skin. The possibility of an attack

has the advantage to the user of forcing the defender into protective

clothing. Trichothecenes are actually very effective blister agents.

The minimal dose of T-2 toxin required to produce skin injury is about

400-fold lower than it is for mustard. Blistering and eye damage are

likely well below exposure to a lethal dose. Inhalation toxicity is

comparable to that of mustard or ite.

These toxins are relatively easy to manufacture. The producer

organisms are robust and can be grown in large fermentation vessels. A

terrorist may be able to make a crude trichothecene preparation by

practicing poor grain husbandry. The Fusarium species that make

trichothecenes grow on staple cereals such as wheat and barley.

Aflatoxin-producing fungi prefer oil-rich seed such as maize (Zea

mays, Indian corn or corn in the US). Outbreaks of alimentary toxic

aleukia (ATA) that killed thousands in an already devastated

post-World War II Soviet Union had their origins in grains left over

winter in the fields under conditions ideal for trichothecene

synthesis. These grains were scant gleanings that would have been left

for the birds in better days.

The toxins would most likely be spread as an aerosol with the yellow

rain used in Indo-China being described as a sticky yellow liquid. The

fungi themselves could be used as an economic weapon against

well-regulated agricultures, such as those of North America and Europe

where the appearance of the disease on any significant scale could

trigger stringent responses including destruction of crops.

Return to Top

Terrorist Acquisition and Attempted Use.

* None confirmed.

Return to Top

International Disease Classification Codes for T-2 Poisoning Disease

ICD-9-CM ICD-10

Toxic effects of aflatoxins &

other mycotoxins as food contaminants

--------------------------------------------------------

http://www.cbwinfo.com/Biological/Toxins/Satra.html

Satratoxin H:

essential data

Symptoms and Treatment, Toxicity, Chemistry, Site of Action,

Sources, Properties, Terrorist Interest, IDC Codes

Symptoms, Treatment, Decontamination

Syndrome Name Stachybotrotoxicosis

Symptoms

* burning and blistering of mouth and nose

* a rash that becomes a moist dermatitis

* nosebleeds

* chest pain

* pulmonary hemorrhage

* hyperthermia (raised temperature)

* headache

* fatigue

* diarrhea

Onset of Symptoms Relatively slow (minutes to hours)

Rapid diagnostic assay None

Antidote None

Supportive Care Removal of ingested toxins by treatment with

adsorbents such as superactivated charcoal; treatment of symptoms

Inactivation Decontamination with soap and water.

Toxicology. Satratoxin H has an LD50 for mice of 1.0-1.4 mg/kg upon

intraperitoneal injection. Otherwise, it is reported to be about five

times as toxic as T-2 toxin.

More extensive toxicological information can be found by following

this link.

Chemical Properties

Structure

CA Name Spiro[5,9:16,18-dimethano-1H,3H,23H-[1,6,12]

trioxacyclooctadecino[3,4-d]][1]benzopyran-17

(18H),2'-oxirane]-3-14(9H)dione,6,7,16,16a,19a,22-

hexahydro-25-hydroxy-9-[(1S)-1-hydroxyethyl]-16a,21-

dimethyl,(2'R,4E,9R,10E,12Z,16R,16aS,18R,19aR23aR,25R)-

Trivial Names

* Satratoxin H

Registry Number 53126-64-0

RTECS Number

Molecular

Formula C29 H36 O9

Molecular

weight

Solubility Insoluble in water,

soluble in lower alcohols and polar solvents including

* methanol,

* ethanol,

* isopropanol

* propylene glycol,

* acetone,

* ethyl acetate

* chloroform,

* dimethyl sulfoxide

pKa in water Not applicable

Complete synthesis None

Return to Top

Site of Action

Not known,but like most of the other trichothecene mycotoxins

considered for use as weapons act by inhibiting protein synthesis

affecting tissues where cells are actively and rapidly growing and

dividing.

Source

Stachybotrys chartarum, also known as Stachybotrys atra and

Stachybotrys alternans in older publications.

Return to Top

Agent Properties

Unlike T-2 toxin, satratoxin H does not appear to be particularly

effective as a blistering agent on the skin, but is effective against

moist tissues such as the mouth, nose, and throat.

The producer organism grows readily in damp environments, such as damp

hay and has become recognized as a public health problem in houses

that have become damp, e.g. through flooding, because it growth on

cellulosic substrates such as the paper covering of wallboard.

It may not be necessary to isolate toxins from cultures as the spores

and fragments of the fungal mass are themselves effective carriers of

the toxins.

Terrorist Acquisition and Attempted Use.

* None confirmed.

Return to Top

International Disease Classification Codes for Satratroxin H Poisoning

Disease ICD-9-CM ICD-10

Toxic effects of aflatoxins &

other mycotoxins as food contaminants

----------------------------------

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...