The New Synthetic Monophenolic Antioxidant TS-13 Penetrates the Blood–Brain Barrier

TS-13 (sodium 3-(3'-tert-butyl-4'-hydroxyphenyl)propyl thiosulfonate) is a synthetic antioxidant that in numerous studies has demonstrated biological effectiveness in modeling pathological conditions in vivo, in particular, in the model of Parkinson’s disease. To establish whether these effects are indirect or associated with, among other things, the direct effect of TS-13 on the organs and tissues of animals, in this work we determined the concentration of TS-13 in the blood plasma and brain of rats after intragastric administration. After a single intragastric injection of TS-13 solution at a dose of 100 mg/kg to male Sprague Dawley rats (n = 57), biomaterial (blood, brain) was collected over 24 h. To measure the concentration of a substance in samples, a bioanalytical technique using high-performance liquid chromatography with UV detection was developed and validated. The quantitative determination method was developed by us for the first time and validated before the study. It has been established that the calculated values of the calibration samples meet the acceptance criteria (have the required accuracy and precision) in the concentration range from 0.05 to 6 μg/mL, R = 0.9998. The results of determining the concentration of TS-13 in the blood plasma and brain of rats showed that after a single oral administration the compound enters the blood, where it is detected within 15 h (average retention time 7.94 h, half-life 7.59 h, elimination constant 0.13 h–1, total clearance 40.1 L/(kg h)), and also penetrates the blood–brain barrier, quickly entering the brain (maximum concentration is achieved after 1 h). The compound has low affinity for brain tissue (tissue availability 0.32), and, therefore, its concentration does not reach high values; however, slow elimination of the substance is observed—average retention time 6.56 h, half-life 6.43 h, elimination constant 0.11 h–1. After a single intragastric administration to rats, TS-13 enters the blood, where at least part of it is detected unchanged after 30 min, reaching maximum values after 1 h. A similar kinetics of the substance is characteristic of the brain, where it is found in smaller quantities. Thus, as a result of the study, it was shown that TS-13 penetrates the blood–brain barrier and is able to directly affect brain structures, which, however, does not negate the possibility of an indirect effect, mediated by the ability to change the activity of intra- and intercellular signaling systems.

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Publication Details

Journal
Cell and Tissue Biology
Published
2024-08-12
DOI
https://doi.org/10.1134/s1990519x24700457
Primary Topic
Genomics, phytochemicals, and oxidative stress
Type
article
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article

The New Synthetic Monophenolic Antioxidant TS-13 Penetrates the Blood–Brain Barrier

M. V. Khrapova, Yu. G. Zyuz’kova, O. S. Bryushinina, E. B. Menshchikova et al.
Cell and Tissue Biology
Genomics, phytochemicals, and oxidative stress
article

The New Synthetic Monophenolic Antioxidant TS-13 Penetrates the Blood–Brain Barrier

M. V. Khrapova, Yu. G. Zyuz’kova, O. S. Bryushinina, E. B. Menshchikova, Н. В. Кандалинцева
article en

Abstract

TS-13 (sodium 3-(3'-tert-butyl-4'-hydroxyphenyl)propyl thiosulfonate) is a synthetic antioxidant that in numerous studies has demonstrated biological effectiveness in modeling pathological conditions in vivo, in particular, in the model of Parkinson’s disease. To establish whether these effects are indirect or associated with, among other things, the direct effect of TS-13 on the organs and tissues of animals, in this work we determined the concentration of TS-13 in the blood plasma and brain of rats after intragastric administration. After a single intragastric injection of TS-13 solution at a dose of 100 mg/kg to male Sprague Dawley rats (n = 57), biomaterial (blood, brain) was collected over 24 h. To measure the concentration of a substance in samples, a bioanalytical technique using high-performance liquid chromatography with UV detection was developed and validated. The quantitative determination method was developed by us for the first time and validated before the study. It has been established that the calculated values of the calibration samples meet the acceptance criteria (have the required accuracy and precision) in the concentration range from 0.05 to 6 μg/mL, R = 0.9998. The results of determining the concentration of TS-13 in the blood plasma and brain of rats showed that after a single oral administration the compound enters the blood, where it is detected within 15 h (average retention time 7.94 h, half-life 7.59 h, elimination constant 0.13 h–1, total clearance 40.1 L/(kg h)), and also penetrates the blood–brain barrier, quickly entering the brain (maximum concentration is achieved after 1 h). The compound has low affinity for brain tissue (tissue availability 0.32), and, therefore, its concentration does not reach high values; however, slow elimination of the substance is observed—average retention time 6.56 h, half-life 6.43 h, elimination constant 0.11 h–1. After a single intragastric administration to rats, TS-13 enters the blood, where at least part of it is detected unchanged after 30 min, reaching maximum values after 1 h. A similar kinetics of the substance is characteristic of the brain, where it is found in smaller quantities. Thus, as a result of the study, it was shown that TS-13 penetrates the blood–brain barrier and is able to directly affect brain structures, which, however, does not negate the possibility of an indirect effect, mediated by the ability to change the activity of intra- and intercellular signaling systems.

Cell and Tissue BiologyVol. 18(5)
Russian Academy of Sciences (RU), Tomsk National Research Medical Center (RU), Federal Research Center of Fundamental and Translational Medicine (RU), Novosibirsk State Pedagogical University (RU), Research Institute of Pharmacology and Regenerative Medicine named ED Goldberg (RU)
Openalex Percentile: Top 88%
Genomics, phytochemicals, and oxidative stress
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