Effect of Beta-Adrenergic Agonist Gynipral on the Radical Activity of Neutrophils in the Blood of Women at Different Stages of Reproduction
DOI:
https://doi.org/10.37482/2687-1491-Z055Keywords:
beta-adrenergic receptors, pregnancy, childbirth, Gynipral, neutrophil respiratory burstAbstract
In recent years, the idea about the physiological significance of neutrophils, including during pregnancy and childbirth, has evolved significantly. There is an opinion that in the course of pregnancy, the activity of non-specific cellular immunity increases, which, in addition to performing a protective function, forms a mode of contractile activity of the uterus that is optimal for child-bearing. In obstetric practice, in order to reduce uterine hypertonicity in the treatment of miscarriage, β-adrenergic agonists are widely used. However, many aspects of their influence on the mother and the foetus remain insufficiently studied. The aim of this paper was to study the effect of Gynipral (selective β2-adrenergic agonist) on the intensity of latex-induced respiratory burst of venous blood neutrophils in women at different stages of reproduction. Using the chemiluminescence method, we showed for the first time that Gynipral, depending on the stage of reproduction, has multidirectional effect on the latex-induced radical activity of neutrophils in the venous blood of women in vitro. At a low level of radical reaction of neutrophils to latex (in the follicular phase of the cycle, during pregnancy and, which is especially important, during childbirth), Gynipral enhances the oxidative activity of cells; at a high level of radical reaction of neutrophils (during the luteal phase of the cycle and after childbirth), Gynipral inhibits it. It can be assumed that in women, catecholamines (adrenaline) during pregnancy through β2- and/or β3-adrenergic receptors increase the ability of neutrophils to produce activated forms of oxygen, while after delivery they reduce this ability. Such changes in receptor activation may be associated with the phenomenon of switching of β-adrenergic receptor coupling from Gs protein to Gi protein, which is important for regulatory mechanisms.
For citation: Polezhaeva T.V., Paturova I.G., Zaytseva O.O., Solomina O.N., Khudyakov A.N., Sergushkina M.I., Dmitrieva S.L., Tsirkin V.I. Effect of Beta-Adrenergic Agonist Gynipral on the Radical Activity of Neutrophils in the Blood of Women at Different Stages of Reproduction. Journal of Medical and Biological Research, 2021, vol. 9, no. 2, pp. 171–181. DOI: 10.37482/2687-1491-Z055
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Shynlova O., Nedd-Roderique T., Li Y., Dorogin A., Lye S.J. Myometrial Immune Cells Contribute to Term Parturition, Preterm Labour and Post-Partum Involution in Mice // J. Cell. Mol. Med. 2013. Vol. 17, № 1. Р. 90–102. DOI: 10.1111/j.1582-4934.2012.01650.x
Schumacher M., Mattern C., Ghoumari A., Oudinet J.P., Liere P., Labombarda F., Sitruk-Ware R., De Nicola A.F., Guennoun R. Revisiting the Roles of Progesterone and Allopregnanolone in the Nervous System: Resurgence of the Progesterone Receptors // Prog. Neurobiol. 2014. Vol. 113. Р. 6–39. DOI: 10.1016/j.pneurobio.2013.09.004
Lampé R., Kövér Á., Szűcs S., Pál L., Árnyas E., Póka R. Phagocytic Index of Neutrophil Granulocytes and Monocytes in Healthy and Preeclamptic Pregnancy // J. Reprod. Immunol. 2015. Vol. 107. Р. 26–30. DOI: 10.1016/j.jri.2014.11.001
Naccasha N., Gervasi M., Chaiworapongsa T., Berman S., Yoon B., Maymon E., Romero R. Phenotypic and Metabolic Characteristics of Monocytes and Granulocytes in Normal Pregnancy and Maternal Infection // Am. J. Obstet. Gynecol. 2001. Vol. 185, № 5. Р. 1118–1123. DOI: 10.1067/mob.2001.117682
Segerer S., Kammerer U., Kapp M., Dietl J., Rieger L. Upregulation of Chemokine and Cytokine Production During Pregnancy // Gynecol. Obstet. Invest. 2009. Vol. 67, № 3. Р. 145–150. DOI: 10.1159/000174291
Luppi P., Irwin T., Simhan H., Deloia J. CD11b Expression on Circulating Leukocytes Increases in Preparation for Parturition // Am. J. Reprod. Immunol. 2004. Vol. 52, № 5. Р. 323–329. DOI: 10.1111/j.1600-0897.2004.00229.x
Yuan M., Jordan F., McInnes I., Harnett M., Norman J. Leukocytes Are Primed in Peripheral Blood for Activation During Term and Preterm Labour // Mol. Hum. Reprod. 2009. Vol. 15, № 11. Р. 713–724. DOI: 10.1093/molehr/gap054
Leathersich S.J., Vogel J.P., Tran T.S., Hofmeyr G.J. Acute Tocolysis for Uterine Tachysystole or Suspected Fetal Distress // Cochrane Database Syst. Rev. 2018. № 7. Art. № CD009770. DOI: 10.1002/14651858.CD009770.pub2
Garmi G., Salim R. Medical Therapy for the Management of Preterm Labor: Is There a First Line Agent? // Harefuah. 2015. Vol. 154, № 10. Р. 657–674.
Haram K., Mortensen J.H., Morrison J.C. Tocolysis for Acute Preterm Labor: Does Anything Work // J. Matern. Fetal Neonatal Med. 2015. Vol. 28, № 4. Р. 371–378. DOI: 10.3109/14767058.2014.918095
Lamont C.D., Jоrgensen J.S., Lamont R.F. The Safety of Tocolytics Used for the Inhibition of Preterm Labour // Expert Opin. Drug Saf. 2016. Vol. 15, № 9. Р. 1163–1173. DOI: 10.1080/14740338.2016.1187128
Carvajal J.A., Zambrano M.J., Theodor N.M., Moreno L.E., Olguín T.R., Vanhauwaert P.S., Rojas N.B., Delpiano A.M. The Synergic in vitro Tocolytic Effect of Nifedipine Plus Ritodrine on Human Myometrial Contractility // Reprod. Sci. 2017. Vol. 24, № 4. P. 635–640. DOI: 10.1177/1933719116667221
Качина И.И., Шилов Д.Ю. Влияние агониста бета-адренорецепторов in vitro на фагоцитарную активность нейтрофилов периферической крови здоровых людей // Вестн. Урал. мед. акад. науки. 2012. № 4. С. 40.
Шилов Д.Ю., Годовалов А.П., Шилов Ю.И., Юркова Е.В. Влияние агониста бета-адренорецепторов гексопреналина сульфата на пролиферативный ответ лимфоцитов и продукцию иммуноглобулинов в присутствии тироксина и дексаметазона фосфата in vitro // Фундам. исследования. 2011. № 6. С. 192–196.
Zabrodskii P.F., Gromov M.S., Maslyakov V.V. Role of β2-Adrenoreceptors in Adrenergic Anti-Inflammatory Mechanism in Sepsis // Bull. Exp. Biol. Med. 2017. Vol. 163, № 6. P. 710–713. DOI: 10.1007/s10517-017-3886-8
Панасенко Л.М., Краснова Е.И., Ефремов А.В. Клиническое значение хемилюминесцентного ответа лейкоцитов крови при коклюше // Бюл. Сиб. отд-ния РАМН. 2005. Т. 25, № 3. С. 44–47.
Алексеев Н.А. Клинические аспекты лейкопений, нейтропений и функциональных нарушений нейтрофилов. СПб.: Фолиант, 2002. 416 с.
Polezhaeva T.V., Paturova I.G., Zaitseva О.О., Khudyakov A.N., Bezmeltseva O.M., Sergushkina M.I., Bratukhina O.A., Tsirkin V.I. Intensity of Latex-Induced Respiratory Burst of Neutrophils in the Venous Blood of Women at Different Stages of Reproduction // Hum. Physiol. 2020. Vol. 46, № 1. P. 80–84. DOI: 10.1134/S0362119719060094
Циркин В.И., Ноздрачев А.Д., Анисимов К.Ю., Сизова Е.Н., Полежаева Т.В., Хлыбова С.В., Морозова М.А., Трухин А.Н., Коротаева Ю.В., Куншин А.А. Механизмы положительной и отрицательной модуляции эффективности активации адренорецепторов и других рецепторов, ассоциированных с G-белком (обзор литературы). Сообщение 1. Десенситизация и эндогенные сенсибилизаторы рецепторов (ЭСААР, ЭСН1ГР и ЭСМХР) // Вестн. Урал. мед. акад. науки. 2016. № 2. С. 147–169. DOI: 10.22138/2500-0918-2016-14-2-147-169
Sakakibara T., Inoue Y., Uzue S., Tsukamoto T., Kobayashi M., Kojima M., Akahane M., Kitamura K., Kawarabayashi T. Diversity of Inhibitory Responses to β2-Stimulants Shown by Term-Pregnant Human Myometria in vitro Is Partly Due to Differences in Receptor Density // Am. J. Obstet. Gynecol. 2002. Vol. 186, № 5. Р. 997–1004. DOI: 10.1067/mob.2002.122412
Chanrachakul B., Broughton Pipkin F., Khan R.N. Contribution of Coupling Between Human Myometrial β2-Adrenoreceptor and the BK(Ca) Channel to Uterine Quiescence // Am. J. Physiol. Cell. Physiol. 2004. Vol. 287, № 6. Р. С1747–С1752. DOI: 10.1152/ajpcell.00236.2004
Bardou M., Rouget C., Breuiller-Fouché M., Loustalot C., Naline E., Sagot P., Frydman R., Morcillo E.J., Advenier C., Leroy M.J., Morrison J.J. Is the Beta3-Adrenoceptor (ADRB3) a Potential Target for Uterorelaxant Drugs? // BMC Pregnancy Childbirth. 2007. Vol. 7, Suppl. 1. Art. № S14. DOI 10.1186/1471-2393-7-S1-S14
Liu R., Ramani B., Soto D., De Arcangelis V., Xiang Y. Agonist Dose Dependent Phosphorylation by Protein Kinase A and G Protein-Coupled Receptor Kinase Regulates β2 Adrenoceptor Coupling to Gi Proteins in Cardiomyocytes // J. Biol. Chem. 2009. Vol. 284, № 47. Р. 32279–32287. DOI: 10.1074/jbc.M109.021428
Woo A.Y.-H., Song Y., Xiao R.-P., Zhu W. Biased β2-Adrenoceptor Signalling in Heart Failure: Pathophysiology and Drug Discovery // Br. J. Pharmacol. 2015. Vol. 172, № 23. Р. 5444–5456. DOI: 10.1111/bph.12965