SEVOFLURANE EFFECT ON HUMAN NEUTROPHILS
https://doi.org/10.34822/2304-9448-2022-1-80-85
Abstract
The study aims to analyze the effect of sevoflurane on human neutrophils under normal and pathological conditions. Materials and methods. In the course of the research, the culture of neutrophils isolated from venous blood of donors was studied. The exposure of neutrophils was carried out with the minimal alveolar concentration of sevoflurane of 0.5, 1.0 and 1.5, evaluating the anesthetic effect on their activation. The apoptosis
intensity was assessed using annexin V and propidium iodide. Neutrophils activation with lipopolysaccharide and chemotaxis peptide N-formyl-methionine-leucine-phenylalanine was determined by the level of expression of neutrophil degranulation markers CD11b and CD66b, interleukin-1β, interleukin-6, interleukin-8 and phosphorylation of glycogen synthase kinase-3β. The statistical processing was carried out using math-and-stats methods of calculation of the basic measures of sampling distribution (arithmetic average, standard deviation, Student criterion, nonparametric methods), using Windows and Statistica 10.0 package. Results. Neutrophils
incubation with lipopolysaccharide (200 ng/ml) and N-formyl-methionine-leucine-phenylalanine (100 nM) statistically doubled the expression of CD11b and CD66b molecules, but the exposure to sevoflurane at the minimal alveolar concentration dose of 1.5 reduced the anti-inflammatory activation of neutrophils under the influence of lipopolysaccharide. Stimulation of neutrophils with lipopolysaccharide was accompanied with dephosphorylation of GSK-3β, and the exposure to the minimal alveolar concentration of sevoflurane of 1.5 contributed to its
phosphorylation. It is noted that phosphorylation of GSK-3β in neutrophils reduces the expression of CD11b and CD66b under the influence of sevoflurane.
About the Authors
D. O. StarostinRussian Federation
Assistant Professor
E-mail: starostin_daniil@mail.ru
V. T. Dolgikh
Russian Federation
Honored Worker of Science of the Russian Federation, Doctor of Sciences (Medicine), Professor
E-mail: prof_dolgih@mail.ru
A. N. Kuzovlev
Russian Federation
Doctor of Sciences (Medicine), Associate Professor
E-mail: artem_kuzovlev@mail.ru
O. A. Grebenchikov
Russian Federation
Doctor of Sciences (Medicine)
E-mail: oleg.grebenchikov@yandex.ru
References
1. Долгих В. Т., Корпачева О. В., Ершов А. В. Патофизиология. В 2 т. Т. 2. Частная патофизиология. М. : Юрайт, 2020. 351 с.
2. Пасечник А. В., Фролов В. А., Моисеева Е. Г., Илларионова Т. С., Мангасаров А. Г., Хоменко А. А., Гасс М. В., Фатхи Н. Ф. Анализ воспалительного процесса в параметрах функции нейтрофилов // Вестник РУДН. Сер.: Медицина. 2001. № 3. C. 33–36.
3. Балабекова М. К. Состояние иммунного статуса интактных крыс с асептическим воспалением: экспериментальное исследование // Вестник КазНМУ. 2010. № 5. С. 278–281.
4. Образцов И. В., Годков М. А., Кулабухов В. В., Владимирова Г. А., Измайлов Д. Ю., Проскурина Е. В. Функциональная активность нейтрофилов при ожоговом сепсисе // Общая реаниматология. 2017. Т. 13, № 2. С. 40–51. DOI 10.15360/1813-9779-2017-2-40-51.
5. Гребенчиков О. А., Касаткина И. С., Каданцева К. К., Мешков М. А., Баева А. А. Влияние лития хлорида на активацию нейтрофилов под действием сыворотки пациентов с септическим шоком // Общая реаниматология. 2020. Т. 16, № 5. С. 45–55. DOI 10.15360/1813-9779-2020-5-45-55.
6. Serhan C. N., Levy B. D. Resolvins in Inflammation: Emergence of the Pro-Resolving Superfamily of Mediators // J Clin Invest. 2018. Vol. 128, Is. 7. P. 2657–2669. DOI 10.1172/JCI97943.
7. Beck-Schimmer B., Baumann L., Restin T. et al. Sevoflurane Attenuates Systemic Inflammation Compared with Propofol, but Does not Modulate Neuro-Inflammation: A Laboratory Rat Study // Eur J Anaesthesiol. 2017. Vol. 34, Is. 11. P. 764–775. DOI 10.1097/ EJA.0000000000000668.
8. Koutsogiannaki S., Hou L., Babazada H. et al. The Volatile Anesthetic Sevoflurane Reduces Neutrophil Apoptosis via Fas Death Domain–Fas-Associated Death Domain Interaction // FASEB J. 2019. Vol. 33, Is. 11. P. 12668–12679. DOI 10.1096/fj.201901360R.
9. Rodríguez-González R., Baluja A., Veiras Del Río S. et al. Effects of Sevoflurane Postconditioning on Cell Death, Inflammation and TLR Expression in Human Endothelial Cells Exposed to LPS // J Transl Med. 2013. Vol. 11, Is. 1. P. 87. DOI 10.1186/1479-5876-11-87.
10. Schilling T., Kozian A., Senturk M. et al. Effects of Volatile and Intravenous Anesthesia on the Alveolar and Systemic Inflammatory Response in Thoracic Surgical Patients // Anesthesiology. 2011. Vol. 115, Is. 1. P. 65–74. DOI 10.1097/ALN.0b013e318214b9de.
11. Hayes J. K., Havaleshko D. M., Plachinta R. V., Rich G. F. Isoflurane Pretreatment Supports Hemodynamics and Leukocyte Rolling Velocities in Rat Mesentery during Lipopolysaccharide-Induced Inflammation // Anesth Analg. 2004. Vol. 98, Is. 4. P. 999–1006. DOI 10.1213/01.ANE.0000104584.91385.1D.
12. Braz M. G., Braz L. G., Barbosa B. S. et al. DNA Damage in Patients who Underwent Minimally Invasive Surgery under Inhalation or Intravenous Anesthesia // Mutat Res. 2011. Vol. 726, Is. 2. P. 251–254. DOI 10.1016/j.mrgentox.2011.09.00.
13. Park D. W., Jiang S., Liu Y. et al. GSK3β-Dependent Inhibition of AMPK Potentiates Activation of Neutrophils and Macrophages and Enhances Severity of Acute Lung Injury // Am J Physiol Lung Cell Mol Physiol. 2014. Vol. 307, Is. 10. P. 735–745. DOI 10.1152/ajplung.00165.2014.
Review
For citations:
Starostin D.O., Dolgikh V.T., Kuzovlev A.N., Grebenchikov O.A. SEVOFLURANE EFFECT ON HUMAN NEUTROPHILS. Vestnik SurGU. Meditsina. 2022;(1 (51)):80-85. (In Russ.) https://doi.org/10.34822/2304-9448-2022-1-80-85