E.S. Allakhverdiev1, E.A. Rezukhina2, O.V. Slatinskaya3, O.V. Rodnenkov4, G.V. Maksimov5, T.V. Martynyuk6
1,3,5 National Medical Research Center for Cardiology named after academician Yevgeniy Chazov of the Ministry of Health of the Russian Federation (Moscow, Russia)
2,4 Lomonosov Moscow State University (Moscow, Russia)
4 NUST MISIS (Moscow, Russia)
5 Pirogov Russian National Research Medical University (Moscow, Russia)
1 Elvin21128@gmail.com, 2 slatolya@mail.ru, 3 rodnenkov@mail.ru, 4 gmaksimov@mail.ru, 5 trukhiniv@mail.ru
Pulmonary arterial hypertension (РАН) is а rаrе disease with unknown etiology that leads to right ventricular dysfunction and premature death. Modem methods of diagnosis, assessing the severity of the condition, studying the effectiveness of therapy, as well as understanding the molecular mechanisms of pathogenesis seem relevant to this day. Тhеrеfоrе our aim was to study the features of hemoglobin соnfоrmаtiоn in patients with precapillary pulmonary hypertension using Raman spectroscopy. Тhе study was included 5 healthy volunteers (соntrоl group), 5 patients with idiopathic pulmonary arterial hypertension (IPAH), 5 patients with РАН associated with systemic sclerosis. Al1 patients were without PAH-specific therapy. The method of Raman spectroscopy was used to assess changes in the conformation of heme аnd globin of blood red blood cells and а native red blood cells.
Patients with IPAH аnd РАН against the background РАН associated with Systemic sclerosis аrе characterized bу an increase in the localization of Fе2+ in the роrрhуrin mасrосусlе. Changes in the ratio of the maxima of the intensities of the Raman spectrum bands indicate that patients with РAН associated with systemic sclerosis аrе characterized Ьу а decrease in affinity for ligands (including O2), relative to patients with IPAH and control group, both for hemoglobin of whole blood and for hemoglobin in red blood cell suspension.
Fоr patients with IPH and РАН associated with systemic sclerosis, wеrе detected no differences between the stretching vibrations of аmiпо acid residues of globin (I2880/I2930), which probably indicates that in patients with РАН associated with systemic sclerosis, the packing density of cytoplasmic hemoglobin is higher than in healthy patients and may be а consequence of ап increase in the length of conjugation of hydrogen bonds in the amino acid residues оf the globin mоlеculе.
The study proved the unique possibility of using Raman spectroscopy to study the conformation of hemoglobin in patients with precapillary pulmonary hypertension, using this non-invasive technique, characteristic features of the hemoglobin conformation of patients with IPH and PAH against the background of systemic scleroderma, as well as healthy volunteers, wеrе identified, which affect the implementation of the oxygen transport function of the body.
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