Page last updated: 2024-10-21

amitrole and Dyskinesia, Drug-Induced

amitrole has been researched along with Dyskinesia, Drug-Induced in 1 studies

Amitrole: A non-selective post-emergence, translocated herbicide. According to the Seventh Annual Report on Carcinogens (PB95-109781, 1994) this substance may reasonably be anticipated to be a carcinogen. (From Merck Index, 12th ed) It is an irreversible inhibitor of CATALASE, and thus impairs activity of peroxisomes.
amitrole : A member of the class of triazoles that is 1H-1,2,4-triazole substituted by an amino group at position 3. Used to control annual grasses and aquatic weeds (but not on food crops because it causes cancer in laboratory animals). Its use within the EU was banned from September 2017 on the grounds of potential groundwater contamination and risks to aquatic life; there have also been concerns about its endocrine-disrupting properties.

Dyskinesia, Drug-Induced: Abnormal movements, including HYPERKINESIS; HYPOKINESIA; TREMOR; and DYSTONIA, associated with the use of certain medications or drugs. Muscles of the face, trunk, neck, and extremities are most commonly affected. Tardive dyskinesia refers to abnormal hyperkinetic movements of the muscles of the face, tongue, and neck associated with the use of neuroleptic agents (see ANTIPSYCHOTIC AGENTS). (Adams et al., Principles of Neurology, 6th ed, p1199)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
AbĂ­lio, VC1
Silva, RH1
Carvalho, RC1
Grassl, C1
Calzavara, MB1
Registro, S1
D'Almeida, V1
Ribeiro, Rde A1
Frussa-Filho, R1

Other Studies

1 other study available for amitrole and Dyskinesia, Drug-Induced

ArticleYear
Important role of striatal catalase in aging- and reserpine-induced oral dyskinesia.
    Neuropharmacology, 2004, Volume: 47, Issue:2

    Topics: Aging; Amitrole; Animals; Catalase; Dopamine Agonists; Dyskinesia, Drug-Induced; Enzyme Inhibitors;

2004