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Animal models cont

TABLE 12.14 Selected Experimental Animal Model Data in Support of Lead Neuroepidemiological Findings—(cont.) ... [Pg.479]

TABLE 12.15 Illustrative Multisystem Toxicological Mechanisms for Lead Effects Relevant to CNS of Humans and Animal Models of Lead Toxicity In Vitro and In Vivo Studies—(cont.)... [Pg.487]

D.T. Hill and C. Barth. A dynamic model for stimulation of animal waste digestion. Wat. Poll. Cont. Ass., 10 2129-2143, 1977. [Pg.198]

Figure 7 Mean infection scores of P. ctm nti cysts in homogenates of lung tissues in our four-day cyst reduction model (41). Immunosuppressed rats were allowed to develop heavy P. carinii infections, they were treated with LY303366 for up to 4 days, and the numbers of cysts in the lungs were counted microscopically. Treatment groups were A, animah receiving a single 10 mg IV dose 4 days prior to necropsy B, animals receiving a single 5 mg/kg IV dose 4 days prior and daily 5 mg/kg oral doses on days 1—4 prior to necropsy C, animals receiving daily oral doses on days 1-4 prior to necropsy. Infected control (Inf. cont.) animals received no therapy for P. carinii pneumonia. Figure 7 Mean infection scores of P. ctm nti cysts in homogenates of lung tissues in our four-day cyst reduction model (41). Immunosuppressed rats were allowed to develop heavy P. carinii infections, they were treated with LY303366 for up to 4 days, and the numbers of cysts in the lungs were counted microscopically. Treatment groups were A, animah receiving a single 10 mg IV dose 4 days prior to necropsy B, animals receiving a single 5 mg/kg IV dose 4 days prior and daily 5 mg/kg oral doses on days 1—4 prior to necropsy C, animals receiving daily oral doses on days 1-4 prior to necropsy. Infected control (Inf. cont.) animals received no therapy for P. carinii pneumonia.



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