Skip to main content
. 2022 Jan 6;12:796867. doi: 10.3389/fimmu.2021.796867

Table 1.

Preclinical studies on the effect of systemic inflammation in mouse models for AD.

Mouse model Age at first insult Insult Stimulus source Sacrification time after last insult Effect Reference
APP/PS1 2 and 12 months 2 µg LPS i.h. S. abortus equi, Sigma 7 days Decreased Aβ deposits;
Increased microglial immunoreactivity;
Decreased CD45 immunoreactivity.
(50)
9 months 0.5 mg/kg LPS i.p.
once a week for 13
weeks
E. coli 0111:B4, Sigma 4 hours Decreased Aβ deposits;
Increased neuroinflammatory reaction;
Elevated lysosomal protease cathepsin Z, APP, APOE, CLU.
(51)
3 months 3 µg i.p. LPS once per week for 12 weeks E. coli 055:B5, Sigma Directly after last injection Increased Aβ deposits. (46)
25 months 4 µg LPS i.h. S. typhimurium, Sigma 7 days Decreased Aβ deposits;
Infiltration of BM-derived monocytic cells.
(52)
11 or 16 months 4 µg LPS i.h. S. abortus equi, Sigma 7 days Decreased Aβ deposits;
Microglial activation.
(53)
11 ± 4 months 1.5 µg LPS i.p. once per week for 12 weeks E. coli 055:B5, Sigma Directly after last injection Increased Aβ deposits;
Microglial activation.
(45)
5 and 15 months 1 mg/kg LPS i.p. Ultrapure LPS, S. typhimurium, #L6143, Sigma. 2 and 10 days Increased Aβ deposits and impairing microglial Aβ clearance;
NLRP3 inflammasome activation.
(40)
4 and 13–16 months 0.2 mg/kg LPS i.p.
once a day for 2 days
E. coli O127:B8, #L 3129, Sigma;
S. typhimurium, #L 6511, Sigma
24 hours and 3 months Decreased neuronal complexity;
Impaired long-term potentiation and spatial learning;
NLRP3 inflammasome activation.
(54)
7 months 5 mg/kg LPS i.p. E. coli 055:B5, #L2880, Sigma 24 hours Neuronal Apoptosis;
Microglial activation;
Aggravated cognitive impairment.
(55)
4.5 months 0.1 mg/kg LPS i.v. E. coli 0111:B4, Sigma 4 hours Inflammatory reactions;
Sex-specific hippocampal metabolic signatures;
Sickness behaviors.
(56)
APP23 3 months 10 mg/kg LPS i.p. E. coli 0111:B4, Sigma 0, 1, 3, and 12 hours Increased neuroinflammatory reaction;
Increased vulnerability of the BBB;
Severe sickness behaviors.
(57)
3 months 0.5 mg/kg LPS i.p. once or once a day for 4 days S. typhimurium, Sigma 5 days, 3, 6, and 9 months Modified pathological features. (58)
3xtg-AD 3 and 4.5 months 0.25 mg/kg LPS i.p. twice a week for 4 weeks E. coli 0111:B4, Sigma. Directly after last injection AβPP β-CTP was increased intraneuronal, but Aβ was unchanged. (59)
4 months 0.5 mg/kg LPS i.p. twice per week for 6 weeks E. coli 055:B5, Sigma 24 hours No effect on Aβ deposits;
Inducing tau hyperphosphorylation.
(60)
4 months 1 mg/kg LPS i.p. E. coli
055:B5, Sigma
6 weeks long-term impairment on hippocampal neurogenesis and memory. (61)
6 months 0.5mg/kg i.p. twice a week for 6 weeks E. coli 055:B5, Sigma 6 weeks Increased neuroinflammatory reaction;
up-regulated γ-secretase;
Worsening of behavior;
5-Lipoxygenase pathway affects key neuropathological features.
(62)
4 months 5 mg/kg Poly I:C i.v. #P9582, Sigma 11 months Increased Aβ deposits. (48)
5-6 and 11-12 months Inoculation with 104 tachyzoites of T. gondii or 40 viable eggs of T. muris by o.g. or i.p. once 5, 7, 9, 35 days Increased pro-inflammatory response;
Increased in immune cell infiltration;
Microglial activation.
(63)
Tg2576 17 months 10 µg i.h. LPS S. abortus equi, Sigma 7 days Decreased Aβ deposits;
Microglial activation.
(64)
16-17 months 4 or 10 µg LPS i.h. S. abortus equi, Sigma 1, 3, 7, 14, 28 days Decreased Aβ deposits;
Microglial and astrocyte activation.
(65)
6 and 16 months 25 µg LPS i.v. E. coli 0111:B4, Sigma 1, 2, 4, 6, 18 hours Increased Aβ deposits transiently;
Inflammatory responses.
(43)
PDAPP 2 months 10 µg LPS i.c.v. daily for two weeks E. coli 0111:B4, Sigma Directly after last injection Increased Aβ deposits;
Microglial and astrocyte activation.
(44)
tgSwe 13 months 50 μg LPS i.p. E. coli 055:B5, #L2880, Sigma 1.5 months Decreased Aβ deposits;
Reduced CD45-immunoreactivity.
(66)
5xFAD 3-5 and 13-15 months 0.01, 0.1, 1, 3 mg/kg LPS i.v. once E. coli 0111:B4, Sigma 8 hours Increased BBB permeability. (67)
6 and 13 months 2 µg LPS i.c.v. once or daily Ultrapure LPS, P. gingivalis, In vivoGen 7, 14, 28 days Increased Iba-1 and CD3 positive cells in periventricular area;
No effect on Aβ and cognitive impairment.
(68)
8 months Ligature-induced periodontal disease / 4 weeks Decreased plaque-associated microglia;
Increased insoluble Aβ42 level.
(69)
ME7 8 and 19 weeks post-inoculation with ME7 10 μg LPS i.p. S. abortus equi, Sigma 1.5, 3, 6 and 24 hours Increased levels of IL-1β;
Exaggerated sickness behaviors.
(70)
12, 14 and 15 weeks post-inoculation with ME7 0.1 or 0.5 mg/kg of LPS S. abortus equi, #L5886, Sigma. 2 hours Exacerbated neuronal death and sickness behavior. (71)
18 weeks post-inoculation with ME7 12 mg/kg poly I:C i.p. Amersham Biosciences 3, 15 hours Activated interferon-dependent pro-apoptotic pathways;
Heightened acute sickness behaviour and acute neurological impairments.
(72)
hAPP-J20 62 weeks Inoculation with 109 CFU of live P. gingivalis / 5 weeks Increased Aβ deposits;
Trigger neuroinflammation;
Enhanced cognitive impairments.
(73)
AppNL-G-F 20-23 weeks 1 mg/kg LPS i.p. once a week for 2 weeks S. abortus equi, #L-5886, Sigma 2 weeks Increased Aβ deposits;
Increased microgliosis;
Reduced clearance of Aβ across blood-CSF barrier;
Trigger neuronal dysfunction.
(47)

i.h., intrahippocampal; i.p., intraperitoneal; i.c.v., intracerebroventricular; i.v., intravenous.