THE ROLE OF THE PERIPHERAL SEROTONIN SYSTEM IN THE DEVELOPMENT OF GLUTAMATE-INDUCED OBESITY IN RATS AND ITS CORRECTION BY NANOCRYSTALLINE CERIUM DIOXIDE
M.M. Kondro1, T.I. Halenova2, O.M. Savchuk2, B.M. Vervega1, M.Ya. Spivak3
- Danylo Halytsky Lviv National Medical University
- Taras Shevchenko National University by Kyiv
- D. K. Zabolotny Institute of Microbiology and Virology National Academy of Sciences of Ukraine; Kyiv;
DOI: https://doi.org/10.15407/fz71.04.058

Abstract
Peripheral serotonin is an endocrine regulator of lipid metabo-
lism, as demonstrated in studies on animals with diet-induced
obesity and in observations of obese humans. However, data
on its role in glutamate-induced obesity (GIO) are lacking in
the literature. Therefore, the aim of our work was to study the
functioning of the serotonin system in the blood serum and
duodenal homogenate of rats with GIO, both with and without
treatment with nanocrystalline cerium dioxide (nCeO₂). The
study was carried out on 30 male white rats divided into three
groups: intact, monosodium glutamate (MSG), and MSG +
nCeO₂. Obesity was induced in the MSG and MSG + nCeO₂
groups via neonatal subcutaneous administration of MSG at
a dose of 4 mg/g (dissolved in water for injection, 8 ml/g)
on postnatal days 2, 4, 6, 8, and 10. At one month of age, the
MSG-treated rats were randomly divided into untreated or
nCeO₂-treated groups. The MSG group received water (2.9
ml/kg, orally), while the MSG + nCeO₂ group received a 1
mM solution of nCeO₂ (1 mg/kg, orally). The treatment was
administered over three months in two-week courses (one
course per month). In rats with GIO, blood serum levels of
serotonin and tryptophan were decreased, while monoamine
oxidase (MAO) activity was elevated, contributing to the
М.М. Кондро, Т.І. Галенова, О.М. Савчук, Б.М. Вервега, М.Я. Співак
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reduction in serotonin levels. In the duodenal homogenate,
serotonin content was increased and tryptophan content
was decreased, accompanied by reduced activity of MAO,
tryptophan hydroxylase, and indoleamine 2,3-dioxygenase;
tryptophan decarboxylase activity did not differ significantly
from controls. The course administration of nCeO₂ to MSG-
treated rats had a beneficial effect on these indicators. In
conclusion, the peripheral serotonin system is involved in the
development of obesity regardless of its origin, and nCeO₂
shows potential as a basis for the development of therapeutic
and prophylactic agents.
Keywords:
monosodium glutamate, obesity, serotonin, tryptophan, monoamine oxidase, tryptophan hydroxylase, tryptophan decarboxylase, indoleamine-2,3-dihydrogenase activity
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