Investigation of the optimal dose for experimental lipopolysaccharide-induced recognition memory impairment: behavioral and histological studies

被引:15
|
作者
Alzahrani, Noor Ahmed [1 ]
Bahaidrah, Khulud Abdullah [1 ]
Mansouri, Rasha Abdulrashed [1 ]
Alsufiani, Hadeil Muhanna [1 ]
Alghamdi, Badrah Saeed [2 ,3 ]
机构
[1] King Abdulaziz Univ, Fac Sci, Dept Biochem, Jeddah 21589, Saudi Arabia
[2] King Abdulaziz Univ, Fac Med, Dept Physiol, Neurosci Unit, Jeddah, Saudi Arabia
[3] King Abdulaziz Univ, King Fahd Med Res Ctr, Preclin Res Unit, Jeddah, Saudi Arabia
关键词
Lipopolysaccharide; Neuroinflammation; Recognition memory; Prefrontal cortex; Chronic; Alzheimer disease; Peripheral administration; Recognition memory loss; Novel arm discrimination task; Acute; CAUSES COGNITIVE IMPAIRMENT; MEDIAL PREFRONTAL CORTEX; SYSTEMIC LIPOPOLYSACCHARIDE; ACUTE NEUROINFLAMMATION; OBJECT RECOGNITION; INFLAMMATION; RETRIEVAL; MODEL; HIPPOCAMPUS; FAMILIARITY;
D O I
10.31083/j.jin2102049
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Lipopolysaccharide (LPS) administration is one of the most commonly used methods for inducing inflammation in animal models. Several animal studies have investigated the effects of acute and chronic peripheral administration of LPS on cognitive impairment. However, no previous study has compared the effects of different doses of chronically administered LPS on recognition memory performance. Aim: Here, we aimed to investigate the optimal dose of chronically administered LPS for the induction of recognition memory impairment in mice. Materials and methods: LPS at different doses (0.25, 0.50 and 0.75 mg/kg) was administered to SWR/J mice daily for 7 days. On day 9, the open field, novel object recognition and novel arm discrimination behavioral tests were performed. Additionally, prefrontal cortical histological examination was conducted. Results: Compared with the control group, mice injected with 0.75 mg/kg LPS notably showed no object preference (familiar vs. novel), a reduction in the discrimination index, and spatial recognition impairment. Administration of the 0.25 and 0.50 mg/kg doses of LPS showed a preference for the novel object compared with the familiar object, had no significant impact on the discrimination index, and caused spatial recognition impairment. These behavioral results are in line with the histological examination of the prefrontal cortex, which revealed that the 0.75 mg/kg dose produced the most histological damage. Conclusions: Our findings suggest that for chronic peripheral administration of LPS, 0.75 mg/kg is the optimal dose for inducing neuroinflammation-associated recognition memory deficits.
引用
收藏
页数:10
相关论文
共 50 条
  • [31] Lipopolysaccharide-Induced Striatal Nitrosative Stress and Impaired Social Recognition Memory Are Not Magnified by Paraquat Coexposure
    Goncalves, CinaraLudvig
    dos Santos, Danubia Bonfanti
    Portilho, Sthefani Spricigo
    Lopes, Mark William
    Ghizoni, Heloisa
    de Souza, Viviane
    Mack, Josiel Mileno
    Naime, Aline Aita
    Dafre, Alcir Luiz
    Brocardo, Patricia de Souza
    Prediger, Rui Daniel
    Farina, Marcelo
    NEUROCHEMICAL RESEARCH, 2018, 43 (03) : 745 - 759
  • [32] Hydrogen Sulfide Ameliorates Lipopolysaccharide-Induced Memory Impairment in Mice by Reducing Apoptosis, Oxidative, and Inflammatory Effects
    Viplav Kshirsagar
    Chetan Thingore
    Malvika Gursahani
    Nitin Gawali
    Archana Juvekar
    Neurotoxicity Research, 2021, 39 : 1310 - 1322
  • [33] Effect of Edible Bird's Nest Extract on Lipopolysaccharide-Induced Impairment of Learning and Memory in Wistar Rats
    Careena, S.
    Sani, D.
    Tan, S. N.
    Lim, C. W.
    Hassan, Shariful
    Norhafizah, M.
    Kirby, Brian P.
    Ideris, A.
    Stanslas, J.
    Bin Basri, Hamidon
    Lim, Christopher Thiam Seong
    EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2018, 2018
  • [34] Hydrogen Sulfide Ameliorates Lipopolysaccharide-Induced Memory Impairment in Mice by Reducing Apoptosis, Oxidative, and Inflammatory Effects
    Kshirsagar, Viplav
    Thingore, Chetan
    Gursahani, Malvika
    Gawali, Nitin
    Juvekar, Archana
    NEUROTOXICITY RESEARCH, 2021, 39 (04) : 1310 - 1322
  • [35] Genes Involved by Dexamethasone in Prevention of Long-Term Memory Impairment Caused by Lipopolysaccharide-Induced Neuroinflammation
    Shishkina, Galina T.
    Kalinina, Tatyana S.
    Lanshakov, Dmitriy A.
    Bulygina, Veta V.
    Komysheva, Natalya P.
    Bannova, Anita V.
    Drozd, Ulyana S.
    Dygalo, Nikolay N.
    Zhou, Xian
    BIOMEDICINES, 2023, 11 (10)
  • [36] Aspirin reverts lipopolysaccharide-induced learning and memory impairment: first evidence from an invertebrate model system
    Rivi, Veronica
    Batabyal, Anuradha
    Benatti, Cristina
    Tascedda, Fabio
    Blom, Joan M. C.
    Lukowiak, Ken
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2022, 395 (12) : 1573 - 1585
  • [37] Aspirin reverts lipopolysaccharide-induced learning and memory impairment: first evidence from an invertebrate model system
    Veronica Rivi
    Anuradha Batabyal
    Cristina Benatti
    Fabio Tascedda
    Joan M. C. Blom
    Ken Lukowiak
    Naunyn-Schmiedeberg's Archives of Pharmacology, 2022, 395 : 1573 - 1585
  • [38] GHS-R1a deficiency protects against lipopolysaccharide-induced spatial memory impairment in mice
    Liu, Junru
    Li, Na
    Wei, Chuang
    Han, Fubing
    Deng, Mingru
    Ma, Jialin
    Zou, Xueying
    Zhou, Yu
    Yang, Rong
    Yuan, Haicheng
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2024, 727
  • [39] Enriched dairy fat matrix diet prevents early life lipopolysaccharide-induced spatial memory impairment at adulthood
    Dinel, A. L.
    Rey, C.
    Baudry, C.
    Fressange-Mazda, C.
    Le Ruyet, P.
    Nadjar, A.
    Pallet, P.
    Joffre, C.
    Laye, S.
    PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2016, 113 : 9 - 18
  • [40] Inhibitory effect of ethanol extract of Nannochloropsis oceanica on lipopolysaccharide-induced neuroinflammation, oxidative stress, amyloidogensis and memory impairment
    Choi, Ji Yeon
    Hwang, Chul Ju
    Lee, Hee Pom
    Kim, Hee Sik
    Han, Sang-Bae
    Hong, Jin Tae
    ONCOTARGET, 2017, 8 (28) : 45517 - 45530