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1.
J Inorg Biochem ; 244: 112237, 2023 07.
Artigo em Inglês | MEDLINE | ID: mdl-37105009

RESUMO

Lanthanide cations (La3+ and Tb3+) bind to the Ca-binding site of the oxygen-evolving complex in Ca-depleted PSII membranes and irreversibly inhibit the oxygen evolution. Оn the other hand, EPR measurement of Mn2+ concentration in buffer revealed that lanthanide cations inhibit the light-dependent oxidation of Mn2+ cations via the high-affinity Mn-binding site in Mn-depleted PSII membranes, which suggests that they bind to and inhibit the high-affinity Mn-binding site of the oxygen-evolving complex. The inhibition is irreversible, bound Ln3+ cation could not be washed out from the sample. Calcium ion inhibits oxidation of Mn2+ (5 µM) at very high concentration (tens mM) and the inhibition is reversible. In this work we measured the reduction rate of exogenic electron acceptor 2,6-dichlorophenolindophenol during the oxidation of Mn2+ cations in the Ca-depleted PSII and in the Ca-depleted PSII treated with lanthanides after extraction of Mn cluster from these preparations. We found that irreversible binding of the lanthanide cation to the Ca-binding site in the Ca-depleted PSII membranes leads to a partial inhibition of the high-affinity Mn-binding site.


Assuntos
Oxigênio , Complexo de Proteína do Fotossistema II , Complexo de Proteína do Fotossistema II/química , Transporte de Elétrons , Oxirredução , Cátions , Oxigênio/metabolismo , Sítios de Ligação , Cálcio/metabolismo
2.
Bull Exp Biol Med ; 155(2): 233-5, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24130998

RESUMO

Morphology of erythrocytes and conformation of hemoglobin-derived hematoporphyrin were studied in patients with coronary heart disease (CHD) and patients with circulatory failure using laser interference microscopy and Raman spectroscopy. Correlation was revealed (r=0.81) between hemoglobin oxygen saturation and oxyhemoglobin fraction in erythrocytes evaluated by Raman spectroscopy. Patients with CHD and patients with circulatory failure showed reduced oxygen-releasing capacity of hemoglobin and hemoglobin content and increased oxygen-binding capacity of hemoglobin, and hemoglobin affinity for oxygen. Significant differences from the control were observed only in patients with circulatory failure. It was found that hemoglobin content, hematocrit, and the shape of erythrocytes during CHD and circulatory failure did not differ from the control, whereas the area of erythrocytes was increased.


Assuntos
Doença das Coronárias/sangue , Eritrócitos Anormais/fisiologia , Hemoglobinas/química , Oxigênio/sangue , Choque/sangue , Adulto , Hematócrito , Hematoporfirinas , Humanos , Masculino , Pessoa de Meia-Idade , Consumo de Oxigênio
4.
Aviakosm Ekolog Med ; 41(2): 41-4, 2007.
Artigo em Russo | MEDLINE | ID: mdl-17682504

RESUMO

Plasmatic membrane viscosity and permeability and hemoporphyrine conformation in human hemoglobin were studied on completion of long-duration space flight (LSF). Reversible increases in viscosity and selective permeability (Na+/H+ -turnover) of erythrocyte plasmatic membrane were observed immediately after and in the period of recovery from LSF. Viscosity of lipids in both external and internal locations of plasmatic membrane in human erythrocytes was changed after LSF. The reversible rise of the Na+/H+ -turnover is likely to alter intracellular pH and oxygen binding with hemoglobin. The former is confirmed by the concurrent reversible decline in the deoxyhemoglobin ability to bind oxygen and the oxyhemoglobin ability to retain oxygen. In LSF and during readaptation to the normal gravity blood levels of hemoglobin and free iron are known to be reduced and may be answerable for the hypoxic state of human organism.


Assuntos
Viscosidade Sanguínea/fisiologia , Permeabilidade da Membrana Celular/fisiologia , Membrana Eritrocítica/metabolismo , Hemoglobinas/metabolismo , Consumo de Oxigênio/fisiologia , Oxigênio/metabolismo , Voo Espacial , Seguimentos , Humanos , Concentração de Íons de Hidrogênio , Técnicas Imunoenzimáticas , Líquido Intracelular/metabolismo , Transporte de Íons
5.
Pathophysiology ; 14(1): 41-6, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17403600

RESUMO

Tissue hypoxia, which plays a key role in the development of renal and vascular complications of cardiovascular diseases (CVD), might be considered a consequence of vascular remodeling and/or attenuated oxygen (O(2)) delivery by erythrocytes. Using Raman spectroscopy (RS), we observed that erythrocytes from patients with CVD exhibit changes in the conformation of haemoglobin (Hb) haemoporphyrin (HP), reflecting its lower O(2) transport capacity. Hypertriglyceridemia and hypercholesterolemia are well-known hallmarks of CVD. This study examined the role of plasma lipids in the regulation of erythrocyte membrane viscosity, oxy-Hb content as well as Na(+)/H(+) exchange and Ca(2+)-ATPase, whose activities are altered in patients with CVD. HP conformation was assessed by RS of blood samples. Membrane fluidity was estimated at depths of 0.6-0.8 and 2.2nm by electron-paramagnetic resonance spectroscopy of erythrocytes loaded with spin-labeled 5-doxylstearic acid and 16-doxylstearic acid, respectively. Ion-selective electrodes were employed for the study of H(+) and Ca(2+) fluxes. Both oxy-Hb content and erythrocyte membrane fluidity were decreased in essential hypertension and coronary artery disease patients and negatively correlated with plasma cholesterol but not triglyceride content. This observation allows us to assume that decreased oxy-Hb content in patients with CVD is caused by high plasma cholesterol via attenuation of erythrocyte membrane fluidity and its permeability to O(2). Plasma cholesterol level correlated positively and negatively with erythrocyte Na(+)/H(+) exchange and Ca(2+)-ATPase, respectively. However, in contrast to membrane fluidity, the impact of these ion transporters in oxy-Hb regulation under baseline conditions seems to be negligible. We propose that decreased oxy-Hb content contributes to the reduced O(2) tissue supply seen in patients with CVD.

6.
Ter Arkh ; 77(9): 70-3, 2005.
Artigo em Russo | MEDLINE | ID: mdl-16281494

RESUMO

AIM: To study oxygen supply to erythrocytes in patients with chronic cardiac failure as a factor provoking hypoxia. MATERIAL AND METHODS: The trial enrolled 12 men with chronic cardiac failure (CCF) of functional NYHA class II aged 37 to 74 years (group A). Group B--healthy donors (n = 10) aged 20-40 years. Conformation changes of hemoporphirine were detected with degradation spectroscopy, viscosity of plasmatic membrane--with resonance spectroscopy. Degradation spectroscopy estimated content of Hb-ligant complexes as 0.34 +/- 0.013; complexes I Hb-NO 0.73 +/- 0.11, complexes II Hb-NO 0.28 +/- 0.08 (group A). RESULTS: Electronic-paramagnetic spectroscopy has estimated: S--0.716 +/- 0.005 (group A), 0.667 +/- 0.011 (group B). In group B- 0.5 +/- 0.08; 0.41 +/- 0.22; 0.55 +/- 0.12, respectively. CONCLUSION: Patients with CHF have high microviscosity of plasmatic erythrocytic membrane near location of polar lipid groups; subnormal content of oxyhemoglobin and elevation of the number of complexes of nitric hemoglobin-oxide; altered binding of nitric oxide with hemoglobin.


Assuntos
Baixo Débito Cardíaco/complicações , Membrana Eritrocítica/química , Hematoporfirinas/química , Hipóxia/etiologia , Adulto , Idoso , Membrana Celular/química , Doença Crônica , Espectroscopia de Ressonância de Spin Eletrônica , Eritrócitos/citologia , Hemoglobinas/análise , Hemoglobinas/metabolismo , Humanos , Hipóxia/diagnóstico , Ligantes , Masculino , Pessoa de Meia-Idade , Óxido Nítrico/análise , Consumo de Oxigênio , Oxiemoglobinas/análise , Conformação Proteica , Viscosidade
7.
Biofizika ; 50(2): 310-5, 2005.
Artigo em Russo | MEDLINE | ID: mdl-15856990

RESUMO

The method of spin probe and scanning electron microscopy were used to study the effects of some new synthetic antioxidants and bioregulators, the derivatives of 5-hydroxybenzimidazole, on the membrane structure and morphology of erythrocytes. Analysis of EPR spectra and electron micrographs revealed that the derivatives with various side substituents affect the membrane structure and shape of erythrocytes in a concentration-dependent manner, the effect correlating with the hydrophobic properties of the side derivatives. It was shown that all the compounds in the concentration range 1.10(-7) - 1.10(-3) M exhibit the echinocytogenic action, the most profound effect being found in the compound with benzyl- and ethoxygroup in sites 2 and 5, respectively. Our data suggest that nonelectrolytes, the derivatives of 5-hydroxybenzimidazole, are located in the outer monolayer of erythrocyte membrane.


Assuntos
Antioxidantes/farmacologia , Benzimidazóis/farmacologia , Eritrócitos/ultraestrutura , Animais , Forma Celular/efeitos dos fármacos , Espectroscopia de Ressonância de Spin Eletrônica , Membrana Eritrocítica/efeitos dos fármacos , Membrana Eritrocítica/ultraestrutura , Eritrócitos/efeitos dos fármacos , Técnicas In Vitro , Masculino , Microscopia Eletrônica de Varredura , Ratos , Marcadores de Spin
8.
Pathophysiology ; 11(4): 209-213, 2005 May.
Artigo em Inglês | MEDLINE | ID: mdl-15837166

RESUMO

This study examined the possible involvement of abnormal erythrocyte oxygen (O(2)) transport in the pathogenesis of heart failure. Haemoglobin (Hb) haemoporphyrin conformation was assessed by Raman spectroscopy (RS) of blood samples, whereas membrane fluidity was estimated at depths of 0.6-0.8 and 2.2nm by electron-paramagnetic resonance spectroscopy of erythrocytes loaded with spin-labeled 5-doxylstearic acid and 16-doxylstearic acid, respectively. The fluidity of erythrocyte membranes from patients with heart failure was decreased in the area near the membrane surface and remained unchanged in the deeper hydrophobic membrane regions. The same differences were also detected in healthy controls subjected to chronic high-altitude hypoxia. RS demonstrated that in heart failure the total content of Hb-ligand complexes and the relative content of Hb-nitric oxide (NO) complexes with cleaved Fe(2+)-globin bond was decreased, whereas content of Hb-NO complexes with preserved Fe(2+)-globin bond was increased. We propose that this phenomenon contributes to the reduced O(2) tissue supply seen in patients with heart failure.

9.
Bull Exp Biol Med ; 140(5): 510-3, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16758611

RESUMO

Changes in viscosity and permeability of the plasma membrane and conformation of erythrocyte hemoglobin hematoporphyrin were found in patients with diabetes mellitus. The decrease in oxygen binding and increase in deoxyhemoglobin concentration during diabetes mellitus were accompanied by changes in viscosity and permeability of the membrane for Na+, H+, Ca2+, and K+. Our results suggest that oxygen-binding properties of hemoglobin depend on viscosity and permeability of the erythrocyte plasma membrane.


Assuntos
Membrana Celular/metabolismo , Diabetes Mellitus/sangue , Membrana Eritrocítica/metabolismo , Hemoglobinas/metabolismo , Oxigênio/metabolismo , Cálcio/metabolismo , Estudos de Casos e Controles , Colesterol/metabolismo , Eritrócitos/metabolismo , Hematoporfirinas/química , Homeostase , Humanos , Concentração de Íons de Hidrogênio , Íons , Oxigênio/química , Permeabilidade , Ligação Proteica , Protoporfirinas/metabolismo , Viscosidade
11.
J Gravit Physiol ; 11(2): P79-80, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16235423

RESUMO

The investigation of long-term space flight (SF) effect on the blood cells function is of great importance for modern space biology and medicine. We established that the number of discocytes decreased in the period of early rehabilitation after long-term SF. After SF plasma membrane fluidity and phospholipid content decreased and cholesterol content increased. After SF the amount of haemoglobin decreased and the parameters characterizing haemoglobin haemoporyphyrin (HH) conformation changed. We suppose that erythrocyte shape, membrane fluidity and HH conformation are among factors affecting oxygen transfer during and after space flight.


Assuntos
Membrana Eritrocítica/fisiologia , Eritrócitos/fisiologia , Fluidez de Membrana , Voo Espacial , Ausência de Peso , Colesterol/sangue , Deformação Eritrocítica , Hemoglobinas/fisiologia , Humanos , Fosfolipídeos/sangue , Porfirinas/sangue , Porfirinas/fisiologia
12.
Biofizika ; 47(1): 38-44, 2002.
Artigo em Russo | MEDLINE | ID: mdl-11855288

RESUMO

The capacity of erythrocyte membranes for organic nonelectrolytes from different chemical groups of chemical compounds was studied by the spin probe method and scanning electron microscopy. Hydrophobic spin-labeled derivatives of gamma-carbolin and stearic acid and the screened phenol antioxidant fenozan-1 were used as nonelectrolytes. Based on the analysis of electron spin resonance spectra of the hydrophobic spin-labeled nonelectrolytes and electron micrographs of erythrocytes, differences in the capacity of distribution regions in the intramembrane space of the derivative of gamma-carbolin and fenozan-1, on the one hand, and the spin-labeled derivative of fatty acid, on the other hand, were found. The first group has at least two membrane distribution regions, whereas in the second case only one type of distribution was found. The influence of limited membrane capacity on the realization of biological activity of organic nonelectrolytes is discussed.


Assuntos
Membrana Eritrocítica/metabolismo , Compostos Orgânicos/sangue , Eletrólitos/sangue , Espectroscopia de Ressonância de Spin Eletrônica , Humanos
13.
Izv Akad Nauk Ser Biol ; (4): 508-12, 1996.
Artigo em Russo | MEDLINE | ID: mdl-8991534

RESUMO

Scanning electron microscopy revealed changes in erythrocyte morphology induced by the synthetic antioxidant phenozan-1. Phenozan-1 at 10(-7)-10(-5) M acts as an echinocytogen. This effect of the antioxidant is, probably, due to its distribution in the external monolayer of the erythrocyte membrane and associated structural changes.


Assuntos
Antioxidantes/farmacologia , Membrana Eritrocítica/efeitos dos fármacos , Fenilpropionatos/farmacologia , Relação Dose-Resposta a Droga , Membrana Eritrocítica/ultraestrutura , Humanos , Microscopia Eletrônica de Varredura , Propriedades de Superfície
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