Abstract
Monosodium glutamate (MSG) is a widely used flavour enhancer. A daily intake of MSG at high dosage (2000–4000 mg/kg body weight) is reported to be toxic to humans and experimental animals. The present study aims to investigate the toxic effect of oral administration of MSG at low concentrations (30 and 100 mg/kg body weight) by evaluating biochemical parameters of oxidative stress and inflammation in blood; expression of neuroinflammatory gene and histopathological changes in brain on male Wistar rats. The administration of MSG significantly increases serum level of fasting glucose, insulin, triglycerides, total cholesterol, low-density lipoprotein and decrease level of high-density lipoprotein. Significant low level of FRAP, GSH, SOD, CAT and higher level of MDA, PCO, AOPP, PMRS, NO, CRP, IL-6, TNF-α confirms substantial oxidative stress followed by inflammation after 100 mg MSG treatment. RT-PCR figure shows significant expression of neuroinflammatory gene IL-6 and TNF-α and histopathological examination revealed severe neurodegeneration in hippocampus (CA1 and CA3) and cerebral cortex region of brain at 100 mg MSG treatment. Our result provides evidence that MSG administration at 30 mg does not impose toxicity, however at 100 mg/kg body weight, which is considered a low dose, there is significant toxic effects and may be detrimental to health.
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Data has been shared at https://doi.org/10.17632/mg5bztdgw8.1.
Abbreviations
- MSG:
-
Monosodium glutamate
- BBB:
-
Blood brain barrier
- CA:
-
Cornu ammonis
- NMDAR:
-
N-methyl D-aspartate receptor
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Acknowledgements
The Department of Biotechnology, Government of India, has provided financial support under the ‘Research Resources, Service Facilities, and Platforms’ programme. The Department of Biochemistry is funded by the DST, FIST Grant, New Delhi and the SAP DRS I from UGC.
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Kesherwani, R., Bhoumik, S., Kumar, R. et al. Monosodium Glutamate Even at Low Dose May Affect Oxidative Stress, Inflammation and Neurodegeneration in Rats. Ind J Clin Biochem 39, 101–109 (2024). https://doi.org/10.1007/s12291-022-01077-1
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DOI: https://doi.org/10.1007/s12291-022-01077-1