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. 1997 May 1;17(9):3262–3273. doi: 10.1523/JNEUROSCI.17-09-03262.1997

Table 4.

TNF-α activity (IU/mg protein) in specific brain regions in control, turpentine-, and LPS-treated rats

Control LPS (1 μg, i.c.v.) 1 hr LPS (1 μg, i.c.v.) 3 hr Turpentine 5, 6.5, 8 hr
Hypothalamus Not detectable 63.5  ± 9.8 23.2  ± 3.7 Not detectable
(1.7–2.4) (0.2–2.7)
Hippocampus Not detectable 39.3  ± 8.0 79.1  ± 23.7 Not detectable
(0.9–1.4) (0.6–4.8)
Cerebral cortex Not detectable 11.0  ± 0.8 25.5  ± 2.5 Not detectable
(1.8–4.0) (0.7–3.4)

Rats remained either untreated (control) or were injected either intramuscularly with 50 μl/100 gm turpentine or intra-cerebroventricularly (i.c.v.) with LPS (1 μg/rat). Rats were killed either 1 or 3 hr after LPS or 5, 6.5, or 8 hr after turpentine; brain regions were dissected and homogenized, and TNF-α activity of the resulting supernatants was determined. Values in parentheses are the range of detection limits for each sample.n = 3–4 per group.