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Biomedical subjects

N K Chemeris

Publications and source records attributed to N K Chemeris.

At least 19 recordsLinked to original sources

Lack of direct DNA damage in human blood leukocytes and lymphocytes after in vitro exposure to high power microwave pulses.

Currently, the potential genotoxicity of high power microwave pulses (HPMP) is not clear. Using the alkaline single cell gel electrophoresis assay, also known as the alkaline comet assay, we studied the effects of HPMP (8.8 GHz, 180 ns pulse width, peak power 65 kW, pulse repetition frequency 50 Hz) on DNA of human whole-blood leukocytes and isolated lymphocytes. The cell suspensions were exposed to HPMP for 40 min in a rectangular waveguide. The average SAR calculated from the temperature kinetics was about 1.6 kW/kg (peak SAR was about 300 MW/kg). The steady-state temperature rise in the 50 microl samples exposed to HPMP was 3.5 +/- 0.1 degrees C. In independent experiments, we did not find any statistically significant DNA damage manifested immediately after in vitro HPMP exposure of human blood leukocytes or lymphocytes or after HPMP exposure of leukocytes subsequently incubated at 37 degrees C for 30 min. Our results indicate that HPMP under the given exposure conditions did not induce DNA strand breaks, alkali-labile sites, and incomplete excision repair sites, which could be detected by the alkaline comet assay.

Adult↗

[Aging features in functioning of skin microvascular bed in humans].

The state of skin microcirculation system has been studied in healthy volunteers aged from 20 to 77, using laser Doppler flowmetry. To reveal the reaction of microvascular bed in response to short-term ischemia, occlusive test has been carried out. During experiment the age-induced reduction of microcirculation index has been observed at rest. In response to stopping occlusion the 3.5--4-aliquot increase of microcirculation index has been revealed during reactive post-occlusive hyperemia in all age groups. The data obtained suggest maintenance of high reserve resources of skin microcirculation in ageing in response to ischemia.

Adult↗

[Estimation of age-related changes in the regulation of peripheral blood flow in humans].

The age-dependent features in the state of skin microvascular bed has been studied with laser Doppler flowmetry in healthy volunteers of different age groups. To reveal the reaction of skin blood flow in response to short-term ischemia, the occlusive test has been carried out. To estimate the contribution of rhythmic components to blood flow signal, continuous wavelet-transform spectral analysis was used. Age-dependent increase of pulse-wave amplitude and decrease of respiratory wave amplitude reflecting age-dependent changes in functioning of arteriolar and venular links of microvascular bed have been observed at rest. In response to short-term ischemia the age-dependent reduction of reserve resources has been revealed in functioning of arteriolar link of microvascular bed. The reduction of activity of myogenic, neurogenic and endothelial regulation systems have been shown at rest in ageing.

Adult↗

Effects of low-intensity ultrahigh frequency electromagnetic radiation on inflammatory processes.

Low-intensity ultrahigh frequency electromagnetic radiation (42 GHz, 100 microW/cm(2)) reduces the severity of inflammation and inhibits production of active oxygen forms by inflammatory exudate neutrophils only in mice with inflammatory process. These data suggest that some therapeutic effects of electromagnetic radiation can be explained by its antiinflammatory effect which is realized via modulation of functional activity of neutrophils in the focus of inflammation.

Animals↗

Modulation of the activity of Ca(2+)-activated K+ channels by internal Mg2+ in cultured kidney cells vero.

The inside-out mode of the patch-clamp method was used to study the effects of internal Mg2+ on single large-conductance (193+/-7 pS) Ca(2+)-activated K+ channels in cultured kidney cells. In the absence of Ca2+, Mg2+ (1 to 10 mM) did not activate the channels but modified the activating effect of Ca2+ ions: it decreased the Hill coefficient (n), reduced the apparent dissociation constant (K0.5), and modified the channel open and closed times. K0.5 was found to be a voltage-dependent parameter. In the absence of Mg2+, it averaged 600 microM at -20 mV and 27 microM at +30 mV (22 degrees C, pH 6.8). Mg2+ at saturating concentrations (5 to 10 mM) decreased K0.5 to 50 microM at -20 mV and to 15 microM at +30 mV. Irrespective of the membrane potential, K0.5 tended to its limit value of about 12.6 microM. Thus, the effects of membrane depolarization and Mg2+ exhibited a non-additive, competitive relationship. Mg2+ perturbed the exponential shape of the voltage dependences of K0.5. The Hill coefficient characterizing the interaction of Ca2+ ions with the channels was found to be voltage-dependent. In the absence of Mg2+, it increased rather sharply from approx. 2 to 3.5 when the membrane potential was raised from -10 to 0 mV. Mg2+ increased n in a dose-dependent manner; however, about a twofold increase of n occurred within a narrow concentration range (2 to 3 mM). The action of Mg2+ on n was, apparently, voltage-independent, and the effects of Mg2+ and voltage on n were seemingly additive.

Animals↗

Preliminary microwave irradiation of water solutions changes their channel-modifying activity.

Earlier we have shown that millimetre microwaves (42.25 GHz) of non-thermal power, upon direct admittance into an experiment bath, greatly influence activation characteristics of single Ca(2+)-dependent K+ channels (in particular, the channel open state probability, Po). Here we present new data showing that similar changes in Po arise due to the substitution of a control bath solution for a preliminary microwave irradiated one of the same composition (100 mmol/l KCl with Ca2+ added), with irradiation time being 20-30 min. Therefore, due to the exposure to the field the solution acquires some new properties that are important for the channel activity. The irradiation terminated, the solution retains a new state for at least 10-20 min (solution memory). The data suggest that the effects of the field on the channels are mediated, at least partially, by changes in the solution properties.

Animals↗

Dual effects of microwaves on single Ca(2+)-activated K+ channels in cultured kidney cells Vero.

Using the patch voltage-clamp method, possible effects of millimetre microwaves (42.25 GHz) on single Ca(2+)-activated K+ channels in cultured kidney cells (Vero) were investigated. It was found that exposure to the field of non-thermal power (about 100 microW/cm2) for 20-30 min greatly modifies both the Hill coefficient and an apparent affinity of the channels for Ca2+(i). The data suggest that the field alters both cooperativity and binding characteristics of the channel activation by internal Ca2+. The effects depend on initial sensitivity of the channels to Ca2+ and the Ca2+ concentration applied.

Animals↗

[Effect of the non-hydrolyzable guanosine triphosphate analogue on dopamine modulation of the calcium current in a snail neuron].

Voltage-activated calcium current was recorded in isolated neurons of Lymnaea stagnalis under voltage clamp and intracellular dialysis conditions. Calcium current was modulated by non-hydrolyzable guanine nucleotide analogue, guanosine-5'-0-3-thiotriphosphate (GTP gamma S), in a receptor-mediated manner: effect of 100 microM GTP gamma S was recorded at activation of the dopamine receptor. The results obtained permitted suggesting that the effect of dopamine on calcium channels in these neurons is a GTP-dependent one.

Animals↗

Modulation of calcium current in snail neurones by dopamine: the role of intracellular free calcium.

The inhibition of voltage-gated Ca-current in Limnaea stagnalis (L.) neurones by dopamine cannot be prevented by intracellular administration of the Ca-chelating agent, EGTA. At the same time, substitution of external Ba2+ for Ca2+ substantially weakens the dopamine-induced inhibition. The Ca-ionophore, A23187, also produces an inhibition, but the inhibitory effect of A23187 and of dopamine on Ca-current are non-additive. These findings allow one to suggest that the entry and increase of free Ca concentration presumably in the narrow submembrane space, but not in the bulk of cytoplasm, is important for development of inhibition of neuronal Ca-current by dopamine.

Animals↗

Neurotransmitter-induced modulation of neuronal Ca current is not mediated by intracellular Ca2+ or cAMP.

Dopamine (1 microM) inhibits the Ca component of action potential and corresponding electroexcitable Ca current (ICa) in isolated snail neurons. Adrenaline and serotonin also reduce ICa. The inhibition is not related to changes in intracellular Ca2+ or cAMP concentrations: internal application of 10 mM ethyleneglycoltetraacetic acid or 10 microM cAMP in the mixture with 1 mM Mg-ATP and 2 mM theophylline does not influence the action of neurotransmitters on ICa.

Action Potentials↗

Inhibition of acetylcholine responses by intracellular calcium in Lymnaea stagnalis neurones.

1. Acetylcholine (ACh)-induced currents were studied in completely isolated Lymnaea stagnalis neurones using the voltage-clamp technique. 2. The ACh-activated pathways were shown to be selective for Cl- ions. 3. It was shown that membrane depolarization inhibits ACh-induced conductance. This phenomenon was called 'ACh response inactivation'. 4. Inactivation decreases after lowering the extracellular Ca2+ concentration or after blockade by Mn2+ of the electrically excitable Ca2+ channels. 5. In dialysed neurones an increase of the intracellular Ca2+ concentration inhibits the ACh-induced conductance. 6. The conclusion is made that the inactivation of ACh response by depolarization is initiated by Ca2+ entering the neurone through the electrically excitable Ca channels. 7. The onset and the decay of the ACh response inactivation were studied by analysing the relaxations of the ACh-induced current during and after the application of depolarizing pulses. The most conspicuous relaxation is a slow relaxation observed at the end of a long depolarizing pulse, which appears to reflect the return of the system from the inactivated state to the non-inactivated one. 8. The slow relaxations observed during and after a depolarizing pulse appear correlated with variations of the intracellular Ca2+ concentration, and are distinct from faster relaxations observed in the hyperpolarizing range and attributed to the voltage dependence of the channel open-time.

Acetylcholine↗