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. Author manuscript; available in PMC: 2024 Feb 6.
Published in final edited form as: J Alzheimers Dis. 2022;85(3):1031–1044. doi: 10.3233/JAD-215128

Table 1.

Plasma pharmacokinetics of 125I-Aβ40 and 125I-Aβ42 in WT and APP/PS1 transgenic mice at 8, 24, and 52 weeks

Wild-type
Age (weeks) 125I-Aβ40
125I-Aβ42
Cmax (μCi/mL) AUC (μCi.min/mL) Clearance (mL/min) Cmax (μCi/mL) AUC (μCi.min/mL) Clearance (mL/min)

8 23.2 ± 0.6 63.5 ± 6.5 1.6 ± 0.2 11.3 ± 0.5### 78.9 ± 11.8 1.3 ± 0.2
24 16.4 ± 0.4 43.5 ± 3.1 2.3 ± 0.2 5.2 ± 0.3### 40.1 ± 9.4 2.5 ± 0.3*
52 12.8 ± 0.1 373 ± 63*** 0.26 ± 0.04** 6.0 ± 0.3### 31.2 ± 3.5#### 3.2 ± 0.3***

APP/PS1

8 17.7 ± 1.8 49.7 ± 12.4 2.1 ± 0.5 3.4 ± 0.3### 27.6 ± 9.4 3.6 ± 1.2
24 12.5 ± 0.2 103.0 ± 34.5 1.0 ± 0.3 7.1 ± 0.2## 72.2 ± 19.7 1.4 ± 0.3
52 13.7 ± 0.2 86.8 ± 22.8 1.2 ± 0.3 5.1 ± 1.0### 30.9 ± 7.8 3.2 ± 0.8

Data represent mean±SE, n = 3–5. Significance was assessed over age (*p<0.05, **p<0.01, and ***p<0.001) and 125I-Aβ40 versus 125I-Aβ42 (##p<0.01, ###p<0.001, and ###p<0.0001; two-way ANOVA with Bonferroni post-tests).