Dietary co-exposure to methylmercury and monosodium glutamate disrupts cellular and behavioral responses in the lobster cockroach, Nauphoeta cinerea model

•MeHg + MSG diet reduced total thiol levels in the experimental cockroaches.•TBARS level increased in cockroaches exposed to diet containing MeHg + MSG.•MeHg + MSG diet disrupted locomotor and behavioral parameters in cockroaches.•GST activity was not significantly altered in cockroaches exposed to...

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Published in:Environmental toxicology and pharmacology Vol. 64; pp. 70 - 77
Main Authors: Afolabi, Blessing A., Adedara, Isaac A., Souza, Diogo O., Rocha, João B.T.
Format: Journal Article
Language:English
Published: Netherlands Elsevier B.V 01-12-2018
Elsevier Science Ltd
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Abstract •MeHg + MSG diet reduced total thiol levels in the experimental cockroaches.•TBARS level increased in cockroaches exposed to diet containing MeHg + MSG.•MeHg + MSG diet disrupted locomotor and behavioral parameters in cockroaches.•GST activity was not significantly altered in cockroaches exposed to MeHg + MSG diet.•MeHg + MSG cockroaches decreased the acetylcholinesterase activity. The present study aims to investigate the effect of monosodium glutamate (MSG) both separately and combined with a low dose of methylmercury (MeHg) on behavioral and biochemical parameters in Nauphoeta cinerea (lobster cockroach). Cockroaches were fed with the basal diet alone, basal diet + 2% NaCl, basal diet + 2% MSG; basal diet + 0.125 mg/g MeHg, basal diet + 0.125 mg/g MeHg + 2% NaCl; and basal diet + 0.125 mg/g MeHg + 2% MSG for 21 days. Behavioral parameters such as distance traveled, immobility and turn angle were automatically measured using ANY-maze video tracking software (Stoelting, CO, USA). Biochemical end-points such as acetylcholinesterase (AChE), glutathione-S-transferase (GST), total thiol and TBARS were also evaluated. Results show that MeHg + NaCl, increased distance traveled while MeHg + MSG increased time immobile. AChE activity was significantly reduced in cockroaches across all the groups when compared to the control. There was no significant alteration in GST activity and total thiol levels. It could be that both NaCl and MSG potentiates the neurotoxic effect of MeHg in cockroaches.
AbstractList The present study aims to investigate the effect of monosodium glutamate (MSG) both separately and combined with a low dose of methylmercury (MeHg) on behavioral and biochemical parameters in Nauphoeta cinerea (lobster cockroach). Cockroaches were fed with the basal diet alone, basal diet + 2% NaCl, basal diet + 2% MSG; basal diet + 0.125 mg/g MeHg, basal diet + 0.125 mg/g MeHg + 2% NaCl; and basal diet + 0.125 mg/g MeHg + 2% MSG for 21 days. Behavioral parameters such as distance traveled, immobility and turn angle were automatically measured using ANY-maze video tracking software (Stoelting, CO, USA). Biochemical end-points such as acetylcholinesterase (AChE), glutathione-S-transferase (GST), total thiol and TBARS were also evaluated. Results show that MeHg + NaCl, increased distance traveled while MeHg + MSG increased time immobile. AChE activity was significantly reduced in cockroaches across all the groups when compared to the control. There was no significant alteration in GST activity and total thiol levels. It could be that both NaCl and MSG potentiates the neurotoxic effect of MeHg in cockroaches.
•MeHg + MSG diet reduced total thiol levels in the experimental cockroaches.•TBARS level increased in cockroaches exposed to diet containing MeHg + MSG.•MeHg + MSG diet disrupted locomotor and behavioral parameters in cockroaches.•GST activity was not significantly altered in cockroaches exposed to MeHg + MSG diet.•MeHg + MSG cockroaches decreased the acetylcholinesterase activity. The present study aims to investigate the effect of monosodium glutamate (MSG) both separately and combined with a low dose of methylmercury (MeHg) on behavioral and biochemical parameters in Nauphoeta cinerea (lobster cockroach). Cockroaches were fed with the basal diet alone, basal diet + 2% NaCl, basal diet + 2% MSG; basal diet + 0.125 mg/g MeHg, basal diet + 0.125 mg/g MeHg + 2% NaCl; and basal diet + 0.125 mg/g MeHg + 2% MSG for 21 days. Behavioral parameters such as distance traveled, immobility and turn angle were automatically measured using ANY-maze video tracking software (Stoelting, CO, USA). Biochemical end-points such as acetylcholinesterase (AChE), glutathione-S-transferase (GST), total thiol and TBARS were also evaluated. Results show that MeHg + NaCl, increased distance traveled while MeHg + MSG increased time immobile. AChE activity was significantly reduced in cockroaches across all the groups when compared to the control. There was no significant alteration in GST activity and total thiol levels. It could be that both NaCl and MSG potentiates the neurotoxic effect of MeHg in cockroaches.
Author Adedara, Isaac A.
Afolabi, Blessing A.
Souza, Diogo O.
Rocha, João B.T.
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Keywords Oxidative stress
Monosodium glutamate
Locomotor behavior
Nauphoeta cinerea
Methylmercury
Language English
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Snippet •MeHg + MSG diet reduced total thiol levels in the experimental cockroaches.•TBARS level increased in cockroaches exposed to diet containing MeHg + MSG.•MeHg +...
The present study aims to investigate the effect of monosodium glutamate (MSG) both separately and combined with a low dose of methylmercury (MeHg) on...
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SubjectTerms Acetylcholinesterase
Acetylcholinesterase - metabolism
Animals
Behavior, Animal - drug effects
Blattaria
Cockroaches
Cockroaches - drug effects
Cockroaches - physiology
Diet
Dimethylmercury
Drug Interactions
Exploratory Behavior - drug effects
Glutathione
Glutathione transferase
Locomotion - drug effects
Locomotor behavior
Mercury
Mercury (metal)
Methylmercury
Methylmercury Compounds - toxicity
Monosodium glutamate
Nauphoeta cinerea
Neurotoxicity
Oxidative stress
Parameters
Sodium chloride
Sodium glutamate
Sodium Glutamate - toxicity
Title Dietary co-exposure to methylmercury and monosodium glutamate disrupts cellular and behavioral responses in the lobster cockroach, Nauphoeta cinerea model
URI https://dx.doi.org/10.1016/j.etap.2018.09.003
https://www.ncbi.nlm.nih.gov/pubmed/30300794
https://www.proquest.com/docview/2159930334
Volume 64
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