TY - JOUR
T1 - Bacterial lipopolysaccharide model of neuroinflammation-associated neurodegeneration in Wistar rats
T2 - A comparison between different durations of lipopolysaccharide induction
AU - Blossom, Vandana
AU - Ullal, Sheetal Dinkar
AU - Rai, Rajalakshmi
AU - Chakraborthi, Shrijeet
AU - Kumar, Nayanatara Arun
AU - Pai, Mangala M.
AU - Vadgaonkar, Rajanigandha
N1 - Publisher Copyright:
Copyright: Blossom, et al.
PY - 2024/11
Y1 - 2024/11
N2 - Background and Aim: Bacterial lipopolysaccharide (LPS)-induced neuroinflammation can be the most dependable animal model for studying neurodegeneration mechanisms driven by systemic inflammation-induced neuroinflammation. Hence, this study aimed to standardize the LPS model of neuroinflammation by comparing the effect of relatively low-dose LPS administered for different durations on the induction of neurodegeneration in Wistar rats. Materials and Methods: Six groups of six adult Wistar rats per group were used in the study. Group 1 was the control group, and the other five were administered single weekly dose of LPS (170 µg/kg) for increasing durations, ranging from 4 weeks to 8 weeks. The study endpoints included behavioral parameters, neuronal assay results, and the expression of microglia and astrocytes in the frontal cortex, dentate gyrus, and hippocampus. Results: We observed a significant reduction in the number of neurons and an increase in glial cells at 5 weeks of exposure, along with a decline in memory. Thereafter, these changes were gradual until 7 weeks of exposure. However, at 8 weeks of exposure, there was no further statistically significant worsening compared with the group exposed for 7 weeks. Conclusion: To effectively induce neuroinflammation and cause neuronal damage, a minimum of five weekly LPS administrations at a dose of 170 µg/kg is required. Moreover, our results recommend a maximum of 7 weeks of LPS exposure to create a chronic inflammatory model of neuroinflammation.
AB - Background and Aim: Bacterial lipopolysaccharide (LPS)-induced neuroinflammation can be the most dependable animal model for studying neurodegeneration mechanisms driven by systemic inflammation-induced neuroinflammation. Hence, this study aimed to standardize the LPS model of neuroinflammation by comparing the effect of relatively low-dose LPS administered for different durations on the induction of neurodegeneration in Wistar rats. Materials and Methods: Six groups of six adult Wistar rats per group were used in the study. Group 1 was the control group, and the other five were administered single weekly dose of LPS (170 µg/kg) for increasing durations, ranging from 4 weeks to 8 weeks. The study endpoints included behavioral parameters, neuronal assay results, and the expression of microglia and astrocytes in the frontal cortex, dentate gyrus, and hippocampus. Results: We observed a significant reduction in the number of neurons and an increase in glial cells at 5 weeks of exposure, along with a decline in memory. Thereafter, these changes were gradual until 7 weeks of exposure. However, at 8 weeks of exposure, there was no further statistically significant worsening compared with the group exposed for 7 weeks. Conclusion: To effectively induce neuroinflammation and cause neuronal damage, a minimum of five weekly LPS administrations at a dose of 170 µg/kg is required. Moreover, our results recommend a maximum of 7 weeks of LPS exposure to create a chronic inflammatory model of neuroinflammation.
UR - https://www.scopus.com/pages/publications/85210968850
UR - https://www.scopus.com/inward/citedby.url?scp=85210968850&partnerID=8YFLogxK
U2 - 10.14202/vetworld.2024.2567-2576
DO - 10.14202/vetworld.2024.2567-2576
M3 - Article
AN - SCOPUS:85210968850
SN - 0972-8988
VL - 17
SP - 2567
EP - 2576
JO - Veterinary World
JF - Veterinary World
IS - 11
ER -