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. 2013 Aug 19;154(11):4259–4269. doi: 10.1210/en.2013-1331

Table 1.

Effect of Treatments on Mean LH Concentrations

Treatment Control
Agonist/Antagonist
Before After 0–2 Hours After 2–4 Hours Before After 0–2 Hours After 2–4 Hours
p271 microimplant 8.4 ± 1.5 6.6 ± 0.9 4.8 ± 0.4a 6.8 ± 1.5 5.7 ± 1.0 3.1 ± 0.7a
p271 2 nmol 8.5 ± 2.3 9.0 ± 1.4 9.8 ± 2.1 9.8 ± 1.4 9.7 ± 1.6 10.1 ± 0.9
SB222200 13.2 ± 2.4 13.7 ± 3.9 12.3 ± 3.8 12.5 ± 1.3 11.9 ± 2.3 9.1 ± 2.3a
NKB 9.1 ± 1.5 9.7 ± 1.0 8.9 ± 1.4 10.5 ± 0.8 11.5 ± 1.4 9.6 ± 1.6
BNI 7.6 ± 1.1 9.0 ± 1.4 8.3 ± 1.0 8.1 ± 1.1 10.3 ± 1.3 9.8 ± 1.6
MK-801 6.6 ± 1.4 9.0 ± 2.6 8.2 ± 1.7 7.3 ± 1.5 9.6 ± 2.1 9.9 ± 2.4
Acyline 6.6 ± 1.4 9.0 ± 2.6 8.2 ± 1.7 6.1 ± 1.0 7.7 ± 2.3 7.4 ± 0.2
UFP101 10.9 ± 2.1 11.5 ± 1.4 11.2 ± 1.3 10.3 ± 1.0 12.1 ± 1.3 11.9 ± 1.3

Data presented are mean (±SEM) for time periods before and 0–2 and 2–4 hours after start of treatments. All treatments were via microimplants, except for 2 nmol of p271, which were administered by microinjections.

a

P < .05 vs control (before treatment) values by two-way ANOVA.