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Participation of blood valine and L-arginine-NO system in the development of hyperthermia, the formation of thyroid status and prooxidant-antioxidant state under stress due to bacterial endotoxin

https://doi.org/10.29235/1814-6023-2023-20-2-147-157

Abstract

The importance of free amino acids in the processes of vital activity in normal and pathological conditions is well known. At the same time, there are no data on the role of blood plasma valine in the formation of thyroid status, prooxidant-antioxidant state, and in the development of hyperthermia caused by bacterial endotoxin, although its participation in these processes is quite natural, since valine is an inhibitor of arginase, the activity of which affects the level of arginine amino acid and nitric monoxide (NO). This is important in the regulation of body temperature, lipidperoxidation processes, and the level of iodine-containing hormones. 

The aim of the study was to elucidate the significance of blood plasma valine and the L-arginine-NO system in the formation of thyroid status, prooxidant-antioxidant state and the maintenance of body temperature during stress caused by bacterial endotoxin. 

In experiments on rats and rabbits, it was found that under the conditions of E. сoli lipopolysaccharide action in the body of animals, the pituitary-thyroid gland system, lipid peroxidation (LPO) processes in the blood and liver activate, the nitrate/nitrite (NO3–/NO2–) content increases, the level of valine and arginine in the blood plasma decreases, and body temperature increases. Under the conditions of depression of liver arginase with L-valine (100 mg/kg intraperitoneally 30 minutes before endotoxin injection), the LPS action is not accompanied by an increase in body temperature, leads to less pronounced changes in lipid peroxidation processes, as well as to a more significant decrease in the triiodothyronine content and to an increase in the NO3–/NO2– level in blood plasma in rats. Preliminary administration of the NO synthesis inhibitor L-NAME (25 mg/kg intraperitoneally 30 minutes before endotoxin injection) into the animal body not only reduces body temperature rise and NO3–/NO2– level increase in the blood plasma when acted upon by endotoxin, but also exacerbates changes in the LPO processes in the blood plasma and liver, and prevents the activation of the pituitary-thyroid gland system. 

About the Authors

F. I. Vismont
Belarusian State Medical University
Belarus

Frantishek I. Vismont – Corresponding Member, D. Sc. (Med.), Professor, Head of the Department

83, Dzerzhinski Ave., 220116, Minsk



A. F. Vismont
Belarusian State Medical University
Belarus

Arvid F. Vismont – Ph. D. (Med.), Leading Researcher

83, Dzerzhinski Ave., 220116, Minsk



S. A. Zhadan
Belarusian State Medical University
Belarus

Svetlana A. Zhadan – Ph. D. (Biol.), Associate Professor

83, Dzerzhinski Ave., 220116, Minsk



T. V. Abakumova
Belarusian State Medical University
Belarus

Tatyana V. Abakumova – Assistant

83, Dzerzhinski Ave., 220116, Minsk



F. D. Yakovlev
Belarusian State Medical University
Belarus

Fedor D. Yakovlev – Assistant

83, Dzerzhinski Ave., 220116, Minsk



References

1. Sheibak V. M. Leucine, isoleucine, valine: biochemical foundations for the development of new drugs. Grodno, Grodno State Medical University, 2014. 242 p. (in Russian).

2. Syrovaya A. O., Shapoval L. G., Makarov V. A., Petyunina V. N., Grabovetskaya E. R., Andreeva S. V. [et al.]. Amino acids through the eyes of chemists, pharmacists, biologists. Vol. 2. Kharkiv, Shchedra sadiba plyus Publ., 2015. 268 p. (in Russian).

3. Mayanskii D. N. Kupffer cells and liver pathology. Patologicheskaya fiziologiya i eksperimental’naya terapiya [Pathological physiology and experimental medicine], 1985, vol. 29, no. 4, pp. 80−86 (in Russian).

4. Sehic E., Hunter W. C., Ungar A. L., Blatteis C. M. Blokade of Kupffer cells prevents the belrile and preoptic prostaglandin E2 responses to intravenous lipopolysaccharide in guinea pigs. Annals of the New York Academy of Sciences, 1997, vol. 813, pp. 448–452. https://doi.org/10.1111/j.1749-6632.1997.tb51732.x

5. Taylor B. S., Alarcon L. H., Billiar T. R. Inducible nitric oxide synthase in the liver: regulation and function. Biochemistry, 1998, vol. 63, no. 7, pp. 766–781 (in Russian).

6. Suzuki H., Menegazzi M., Carcereri de Prati A., Mariotto S., Armato U. Nitric oxide in the liver: physiopathological roles. Advances in Neuroimmunology, 1995, vol. 5, no. 4, pp. 379–410. https://doi.org/10.1016/0960-5428(95)00024-0

7. Fabri Z. P., Pashchenko A. E., Zayachuk I. P. Functional activity of the thyroid gland and the distribution of its hormones in peripheral tissues in experimental liver damage. Ukrainskii biokhimicheskii zhurnal [Ukrainian biochemical journal], 1985, vol. 57, no. 2, pp. 84–87 (in Russian).

8. Kelly G. S. Peripheral metabolism of thyroid hormones: a review. Alternativ Medical Review, 2000, vol. 5, no. 4, pp. 306–333.

9. Vismont F. I., Glebov M. A. The role of the detoxification function of the liver in the formation of the thyroid status of the body and thermoregulation. Mediko-biologicheskie problemy zhiznedeyatel’nosti [Medico-biological problems of life], 2013, no. 2, pp. 61–65 (in Russian).

10. Morris S. M. (Jr.). Enzymes of arginine metabolism. Journal of Nutrition, 2004, vol. 134, suppl. 10, pp. 2743S–2747S. https://doi.org/10.1093/jn/134.10.2743S

11. Scibior D., Czeczot H. Arginine – metabolism and functions in the human organism. Postępy Higieny i Medycyny Doświadczalnej, 2004, vol. 58, pp. 321–332 (in Polish).

12. Gerstberger R. Nitric oxide and body temperature control. News in Physiological Sciences, 1999, vol. 14, no. 1, pp. 30–36. https://doi.org/10.1152/physiologyonline.1999.14.1.30

13. Moncada C., Torres V., Varghese G., Albano E., Israel Y. Ethanol-derived immunoreactive species formed by free radical mechanisms. Molecular Pharmacology, 1994, vol. 46, no. 2, pp. 786–791.

14. Holowatz L. A., Kenney W. L. Up-regulation of arginase activity contributes to attenuated reflex cutaneous vasodilatation in hypertensive human. Journal of Physiology, 2007, vol. 581, pt. 2, pp. 863–872. https://doi.org/10.1113/jphysiol.2007.128959

15. Vismont A. F., Vismont F. I. The role of liver arginase and blood urea in the processes of heat transfer, detoxification, formation of thyroid status and thermal stability. Vestsі Natsyyanal’nai akademіі navuk Belarusі. Seryya medytsynskіkh navuk = Proceedings of the National Academy of Sciences of Belarus. Medical series, 2014, no. 2, pp. 48–55 (in Russian).

16. Vismont F. I. Endotoxinemia, dysregulation and the pre-illness formation. Vestsі Natsyyanal’nai akademіі navuk Belarusі. Seryya medytsynskіkh navuk = Proceedings of the National Academy of Sciences of Belarus. Medical series, 2018, vol. 15, no. 1, pp. 7–16 (in Russian).

17. Carvajal N., Cederbaum S. D. Kinetics of inhibition of rat liver and kidney arginase by proline and branched chain amino acids. Biochimica et Biophysica Acta, 1986, vol. 870, no. 2, pp. 181–184. https://doi.org/10.1016/0167-4838(86)90219-0

18. Caldwell R. W., Rodriguez P. C., Toque H. A., Narayanan S. P., Caldwell R. B. Arginase: a multifaceted enzyme important in health and disease. Physiological Reviews, 2018, vol. 98, no. 2, pp. 641–665. https://doi.org/10.1152/physrev.00037.2016

19. Boucher J. L., Moali C., Tenu J. P. Nitric oxide biosynthesis, nitric oxide synthase inhibitors and arginase competition for L-arginine utilization. Cellular and Molecular Life Sciences, 1999, vol. 55, no. 8–9, pp. 1015–1028. https://doi.org/10.1007/s000180050352

20. Geyer J. W., Dabich D. Rapid method for determination of arginase activity in tissue homogenates. Analytical Biochemistry, 1971, vol. 39, no. 2, pp. 412–417. https://doi.org/10.1016/0003-2697(71)90431-3

21. Moshage H., Kok B., Huizenga J. R., Jansen P. L. Nitrite and nitrate determinations in plasma: A critical evaluation. Clinical Chemistry, 1995, vol. 41, no. 6, pt. 1, pp. 892–896.

22. Mihara M., Uchiyama T. Determination of malonaldehyde precursor in tissues by thiobarbituric acid test. Analytical Biochemistry, 1978, vol. 86, no. 1, pp. 271–278.https://doi.org/10.1016/0003-2697(78)90342-1

23. Kostyuk V. A., Potapovich A. I., Lunets E. F. Spectrophotometric determination of diene conjugates. Voprosy meditsinskoi khimii [Problems of medical chemistry], 1984, no. 4, pp. 125–127 (in Russian).

24. Fletcher B. L., Dillard C. L., Tappel A. L. Measurement of fluorescent lipid peroxidation products in biological systems and tissues. Analytical Biochemistry, 1973, vol. 52, no. 1, pp. 1–9. https://doi.org/10.1016/0003-2697(73)90327-8

25. Boboriko T. L., Maslova G. T., Leont’ev V. N. Determination of catalase activity in biological material. Moscow, 1988, dep. at VINITI, no. 1512–B88. (in Russian).

26. Chernyauskene R. Ch., Varshkyavichene Z. Z., Gribauskas P. S. Simultaneous fluorometric determination of the concentrations of vitamins E and A in blood serum. Laboratornoye delo [Laboratory business], 1984, no. 6, pp. 362–365 (in Russian).


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For citations:


Vismont F.I., Vismont A.F., Zhadan S.A., Abakumova T.V., Yakovlev F.D. Participation of blood valine and L-arginine-NO system in the development of hyperthermia, the formation of thyroid status and prooxidant-antioxidant state under stress due to bacterial endotoxin. Proceedings of the National Academy of Sciences of Belarus, Medical series. 2023;20(2):147-157. (In Russ.) https://doi.org/10.29235/1814-6023-2023-20-2-147-157

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ISSN 1814-6023 (Print)
ISSN 2524-2350 (Online)