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Anti-hormonal agents

The specific function of many phytochemicals is still unclear however, a considerable number of studies have shown that they are involved in the interaction of plants/pests/diseases. Most plants produce phytochemicals as anti-microbial, antibiotic, insecticidal and hormonal agents either as part of... [Pg.314]

Secretion of adrenocortical steroids is controlled by the pituitary release of corticotropin (ACTH). Secretion of the salt-retaining hormone aldosterone is primarily under the influence of angiotensin. Corticotropin has some actions that do not depend on its effect on adrenocortical secretion. However, its pharmacologic value as an anti-inflammatory agent and its use in testing adrenal function depend on its secretory action. Its pharmacology is discussed in Chapter 37 and is reviewed only briefly here. [Pg.875]

Anticonvulsants - [ANTI ASTHMATIC AGENTS] (Vol 2) - [HYPNOTICS, SEDATIVES, ANTICONVULSANTS, AND ANXIOLYTICS] (Vol 13) -organobromines as [BROMINE COMPOUNDS] (Vol 4) -sex hormones or [HORMONES - SEX HORMONES] (Vol 13) -use ofbromides [BROMINE COMPOUNDS] (Vol 4)... [Pg.60]

Colchicine (an alkaloid obtained from meadow saffron or autumn crocus) may be used both diagnostically to ascertain the presence of gout and prophylactically to prevent its further occurrence. Usually, 0.5-mg oral doses of colchicine are given hourly until either the therapeutic effects appear or the side effects develop. In addition to colchicine, phenylbutazone, indomethacin, adrenocorticotropic hormone (ACTH), and steroidal anti-inflammatory agents may be used to treat the acute attack of gout. [Pg.277]

Two of the better known "anti-juvenile "Hormone" agents, preco-cenes (9) and fluoromevalonate (10) are inhibitors of JH biosynthesis. The mode of action of fluoromevalonate at the molecular level is unknown. Elucidation of the mode of action of precocenes indicates that these plant chromene derivatives reach the site of JH biosynthesis, the corpora allata (CA), where they undergo a lethal epoxidation leading to extensive macromolecular alkylation and ultimately cause cell death (11, 12). Bioactivation of precocenes to the highly reactive precocene epoxide (13) in the corpora allata is almost certainly catalyzed by methyl farnesoate (MF) epoxidase (14), a cytochrome P-450 sonooxygenase (15) tdtich is the last enzyme of the JH biosynthetic pathway (at least in locusts and cockroaches). [Pg.256]


See other pages where Anti-hormonal agents is mentioned: [Pg.109]    [Pg.515]    [Pg.469]    [Pg.91]    [Pg.410]    [Pg.187]    [Pg.557]    [Pg.358]    [Pg.578]    [Pg.37]    [Pg.8]    [Pg.65]    [Pg.1140]    [Pg.2]    [Pg.7]    [Pg.69]    [Pg.74]    [Pg.444]    [Pg.5]    [Pg.714]    [Pg.766]    [Pg.16]    [Pg.658]    [Pg.108]    [Pg.434]    [Pg.266]    [Pg.242]    [Pg.415]    [Pg.381]    [Pg.181]    [Pg.485]    [Pg.1510]    [Pg.258]    [Pg.453]    [Pg.171]    [Pg.255]    [Pg.256]    [Pg.157]   
See also in sourсe #XX -- [ Pg.205 ]




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