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Monkey Position

Rash central nervous system symptoms (insomnia, irritability, lethargy, dizziness, vivid dreams) usually resolve in 2 weeks increased LFTs false-positive cannabinoid test teratogenic in monkeys... [Pg.1263]

Much of the preclinical data generated with regard to these vaccines entailed the use of one of two animal model systems simian immunodeficiency virus infection of macaque monkeys and HIV infection of chimpanzees. Most of the positive results observed in such systems have been in association with the chimp-HI V model. However, no such system can replace actual testing in humans. [Pg.409]

The other enzyme involved in the synthesis of 5-HT, aromatic L-amino acid decarboxylase (AADC) (EC 4.1.1.28), is a soluble pyridoxal-5 -phosphate-dependent enzyme, which converts 5-HTP to 5-HT (Fig. 13-5). It has been demonstrated that administration of pyridoxine increases the rate of synthesis of 5-HT in monkey brain, as revealed using position emission tomography (this technique is discussed in Ch. 58). This presumably reflects a regulatory effect of pyridoxine on AADC activity and raises the interesting issue of the use of pyridoxine supplementation in situations associated with 5-HT deficiency. [Pg.231]

As a side note, beginning in 1964, a huge open-air biological weapons test was conducted downwind from Johnston Atoll in which a number of ships were positioned around the atoll, upwind from a number of barges stocked with test subjects (rhesus monkeys) who were exposed by agents dispensed from aircraft. [Pg.108]

These three analogues are more metabolically stable than LHRH. Thus, the half-life of nafarelin in monkeys and rats after i.v. administration was four to five times longer than that of LHRH [214], When incubated in monkey plasma, LHRH was readily degraded (f1/2 ca. 2 h), whereas nafarelin was more resistant (tm> 160 h). The metabolism of [14C]nafarelin was also investigated in humans following subcutaneous administration [215]. As shown in Fig. 6.39, the first metabolic steps were cleavage in the 4-5, 5-6, and 7-8 positions. Because of the presence of the 14C-label, the fate of D-2-Nal could be carefully monitored. The same metabolic pattern was observed in the rhesus monkey [216]. [Pg.352]

Paule MG, Allen RR, Bailey JR, Scallet AC, Ali SF, Brown RM, Slikker W Jr. (1992). Chronic marijuana smoke exposure in the rhesus monkey II. Effects on progressive ratio and conditioned position responding. J Pharmacol Exp Ther. 260(1) 210-22. [Pg.564]

Upcn hydrogenation, fish oils, especially the longer chain fatty acids (C22 s), form many new positional and geometric isomers. In some cases, partially hydrogenated fish oils may contain as many as 50% of the docosenoic acids in the trans form as opposed to the naturally occurring cis form. It is these trans isomers which may be responsible for the lipidosis of heart and skeletal muscle found in monkeys. Epidemiological studies of populations with high intakes of docosenoic acids. [Pg.60]

B[/ ]P metabolites have been shown to bind to DNA in culmred human hepatocytes and in human bladder and tracheobronchial explants. The metabolites identified were identical to those produced in other species and differed only in the relative percentages of formation. Human tissues were most active in metabolizing P>[a P and exhibited at least a threefold higher covalent binding of metabolites to DNA than hamsters, dogs, monkeys, or rats. In addition, P>[a P has been tested extensively in several bacterial and mammalian cell systems and has been chosen as a positive control for the validation of some of these systems. ... [Pg.77]


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