TY - JOUR
T1 - Taurine Protects Against Melamine-Induced Hippocampal Neurotoxicity in Rats by Attenuating Metabolic Responses, Autophagy and Inflammation
AU - Atere, Adedeji David
AU - Msibi, Mlungisi Patrick
AU - Oyovwi, Mega Obukohwo
AU - Ben-Azu, Benneth
AU - Seheru, Mepaseka
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Melamine, an industrial chemical linked to neurotoxicity, prompted this study investigating taurine’s neuroprotective effects in rat brains. The study examined the impact of taurine on brain metabolic enzymes, neurochemicals, autophagy-related proteins, and oxidative-inflammatory pathways. Twenty-eight rats were divided into four groups (seven rats per group): control (saline), taurine (100 mg/kg), melamine (50 mg/kg/day), and melamine plus taurine. Taurine administration (30 min post-melamine) continued daily for 28 days, starting on day 29 to day 56, which allowed for the assessment of its restorative effect against ongoing melamine-induced neurotoxicity. Non-spatial recognition memory was evaluated using the novel-object recognition memory test (NORT). Following this, brain neurochemical status, metabolic enzymes, autophagic proteins, and oxidative-inflammatory markers were assessed postmortem. Results demonstrated that taurine improved cognitive function in melamine-treated rats, as evidenced by increased exploration of novel objects in the NORT. Taurine protected against melamine-induced oxidative stress. Additionally, taurine reduce tumor necrosis factor-alpha (TNF-α), interleukin (IL)-6, and IL-1β expression, modulated mammalian target of rapamycin (mTOR) and beclin-1, restored brain metabolic enzyme activity, enhanced neurotransmitter levels, and prevented alterations in α-synuclein and paraoxonase 1 (PON1). In conclusion, taurine protects against melamine-induced neurotoxicity in rats by improving autophagic response, downregulating apoptosis and inflammation markers, inhibiting oxidative stress, and potentially restoring brain metabolic enzyme activities and neurotransmitter levels.
AB - Melamine, an industrial chemical linked to neurotoxicity, prompted this study investigating taurine’s neuroprotective effects in rat brains. The study examined the impact of taurine on brain metabolic enzymes, neurochemicals, autophagy-related proteins, and oxidative-inflammatory pathways. Twenty-eight rats were divided into four groups (seven rats per group): control (saline), taurine (100 mg/kg), melamine (50 mg/kg/day), and melamine plus taurine. Taurine administration (30 min post-melamine) continued daily for 28 days, starting on day 29 to day 56, which allowed for the assessment of its restorative effect against ongoing melamine-induced neurotoxicity. Non-spatial recognition memory was evaluated using the novel-object recognition memory test (NORT). Following this, brain neurochemical status, metabolic enzymes, autophagic proteins, and oxidative-inflammatory markers were assessed postmortem. Results demonstrated that taurine improved cognitive function in melamine-treated rats, as evidenced by increased exploration of novel objects in the NORT. Taurine protected against melamine-induced oxidative stress. Additionally, taurine reduce tumor necrosis factor-alpha (TNF-α), interleukin (IL)-6, and IL-1β expression, modulated mammalian target of rapamycin (mTOR) and beclin-1, restored brain metabolic enzyme activity, enhanced neurotransmitter levels, and prevented alterations in α-synuclein and paraoxonase 1 (PON1). In conclusion, taurine protects against melamine-induced neurotoxicity in rats by improving autophagic response, downregulating apoptosis and inflammation markers, inhibiting oxidative stress, and potentially restoring brain metabolic enzyme activities and neurotransmitter levels.
KW - Autophagy
KW - Inflammation
KW - Melamine
KW - Neurotoxicity
KW - Oxidative stress
KW - Taurine
UR - https://www.scopus.com/pages/publications/105024900735
U2 - 10.1007/s12640-025-00773-z
DO - 10.1007/s12640-025-00773-z
M3 - Article
C2 - 41398135
AN - SCOPUS:105024900735
SN - 1029-8428
VL - 43
JO - Neurotoxicity Research
JF - Neurotoxicity Research
IS - 6
M1 - 53
ER -