Cited by 7Heavy Metal Exposure and ToxicityNitric Oxide and Endothelin EffectsTrace Elements in Health

Elucidation of the Role of L-Arginine and Nω-Nitro-L-Arginine in the Treatment of Rats with Different Levels of Hypoxic Tolerance and Exposure to Lead Nitrate

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Institute of Biology, Pomeranian University in Słupsk, Arciszewski Str. 22b, 76-200 Słupsk, Poland, Tkaczenko, Halina, Lukash, Oleksandr, Kamiński, Piotr, Kurhaluk, Natalia·2024·Cellular Physiology and Biochemistry

Abstract

Background/Aims: Individual resistance to hypoxia is an important feature of the physiological profile of an organism, particularly in relation to lead-induced toxicity. Methods: Our study focused on evaluating parameters of mitochondrial oxygen consumption, microsomal oxidation, intensity of lipoperoxidation processes and antioxidant defences in the liver of rats with low (LR) and high (HR) resistance to hypoxia to elucidate the mechanisms of action of L-arginine and the NO synthase inhibitor L-NNA before or after exposure to lead nitrate. Results: Our study suggests that the redistribution of oxygen-dependent processes towards mitochondrial processes under the influence of the nitric oxide precursor amino acid L-arginine is an important mechanism for maintaining mitochondrial respiratory chain function during per os lead nitrate exposure (3.6 mg lead nitrate/kg bw per day for 30 days). Animals were given L-arginine at a dose of 600 mg/kg bw (i.p., 30 min) before and after exposure to lead nitrate or the NO synthase inhibitor Nω-nitro-L-arginine (L-NNA) at a dose of 35 mg/kg bw (i.p., 30 min) before and after exposure to lead nitrate. Our experiments demonstrated the efficacy of using lead nitrate to simulate lead-related toxic processes via Pb levels in liver tissue; we demonstrated significantly reduced levels of nitrites and nitrates, i.e. stable metabolites of the nitric oxide system, in both LR and HR animals. The effect of the amino acid L-arginine stabilised the negative effects of lead nitrate exposure in both groups of LR and HR rats. We observed the efficiency of mitochondrial energy supply processes and showed a greater vulnerability of NADH-dependent oxidation during lead nitrate exposure in the liver of HR rats. Conclusion: L-arginine initiated the processes of oxidation of NADH-dependent substrates in the LR group, whereas in the HR group this directionality of processes was more effective when the role of the nitric oxide system was reduced (use of L-NNA). Our study of key antioxidant enzyme activities in rat liver tissue during lead nitrate exposure revealed changes in the catalase-peroxidase activity ratio. We found different activities of antioxidant enzymes in the liver tissue of rats treated with lead nitrate and L-arginine or L-NNA, with a significant increase in GPx activity in the LR group when L-arginine was administered both before and after exposure to lead nitrate.

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Crossref · 10.33594/000000716

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Authors
Institute of Biology, P. U. I. S., Tkaczenko, H., Lukash, O., Kamiński, P., & Kurhaluk, N.
Affiliations
  • Uniwersytet Pomorski w Słupsku (PL)
  • Nicolaus Copernicus University (PL)
Corresponding author
Kurhaluk, Natalia
Venue
Cellular Physiology and Biochemistry
Published
2024-07-30
Volume
58
Issue
4
Pages
336-360
ISSN
  • 1015-8987 (ISSN-L)
  • 1421-9778
OpenAlex
W4401113200
Cited by
7
References
74
Citations by year
2026: 1 · 2025: 6
FWCI
1.24
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Cellular Physiology and Biochemistry (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Topics
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Heavy Metal Exposure and Toxicity
  • Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
  • Health Sciences › Nursing › Nutrition and Dietetics › Trace Elements in Health
Keywords
L-arginine, L-NNA, lead nitrate, lead toxicity, hypoxia tolerance, nitric oxide, nitric oxide synthase inhibition, mitochondrial oxygen consumption, microsomal oxidation, lipid peroxidation, antioxidant enzymes, glutathione peroxidase, liver, rats
MeSH terms
Animals, Hypoxia, Arginine, Catalase, Lead, Liver, Male, Mitochondria, Liver, Nitrates, Oxygen Consumption, Lipid Peroxidation, Rats, Wistar, Nitroarginine, Rats

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