Home About us Contact
|
Home About us Contact | ||
|
|
||
Infrared Irradiation (infrared + irradiation)
Selected AbstractsDifferential Long-Term Stimulation of Type I versus Type III Collagen After Infrared IrradiationDERMATOLOGIC SURGERY, Issue 7 2009YOHEI TANAKA MD BACKGROUND The dermis is composed primarily of type I (soft) and type III (rigid scar-like) collagen. Collagen degradation is considered the primary cause of skin aging. Studies have proved the efficacy of infrared irradiation on collagen stimulation but have not investigated the differential long-term effects of infrared irradiation on type I and type III collagen. OBJECTIVE To determine differential long-term stimulation of type I and type III collagen after infrared (1,100,1,800 nm) irradiation. METHODS AND MATERIALS In vivo rat tissue was irradiated using the infrared device. Histology samples were analyzed for type I and III collagen stimulation, visual changes from baseline, and treatment safety up to 90 days post-treatment. RESULTS Infrared irradiation provided long-term stimulation of type I collagen and temporary stimulation of type III collagen. Treatment also created long-term smoothing of the epidermis, with no observed complications. CONCLUSIONS Infrared irradiation provides safe, consistent, long-term stimulation of type I collagen but only short-term stimulation in the more rigid type III collagen. This is preferential for cosmetic patients looking for improvement in laxity and wrinkles while seeking smoother, more youthful skin. [source] Disentangling effects of an experimentally imposed extreme temperature event and naturally associated desiccation on Arctic tundraFUNCTIONAL ECOLOGY, Issue 6 2006F. L. MARCHAND Summary 1Climate projections suggest that extreme events will increase in frequency during this century. As tundra is recognized to be among the most vulnerable biomes, we exposed patches of arctic tundra vegetation to an experimental heatwave (by infrared irradiation), followed by a recovery period. The heating increased the surface temperature with an average of 7·6 °C during 13 days, which slightly exceeded the longest climatic episode with such a temperature deviation since 1961. 2The heatwave decreased stomatal conductance (gs) and PSII maximum efficiency (Fv/Fm), although there were differences in response among the four target species. Salix arctica Pall. (shrub) was affected during the heatwave and could not recover. In Carex bigelowii Tor. ex Schwein (sedge) and Pyrola grandiflora Radius (forb), on the other hand, the effects on gs and Fv/Fm became clear, particularly in the aftermath of the heatwave, whereas Polygonum viviparum L. (forb) was never stressed. 3Effects of the heat on gs were mainly indirect, through increased desiccation, whereas effects on Fv/Fm were more related to leaf temperature (although not in all species). The observed changes can therefore probably be ascribed to a combination of heat and drought causing dysfunctions that ultimately led to senescence. 4Two conclusions of this study, species-specific responses and increased leaf mortality, indicate that more frequent extreme temperature events accompanied by desiccation might alter/endanger tundra communities in a future climate. Predictions of global change effects on arctic ecosystems should therefore take into account the impact of extremes. [source] Species richness and susceptibility to heat and drought extremes in synthesized grassland ecosystems: compositional vs physiological effectsFUNCTIONAL ECOLOGY, Issue 6 2004L. VAN PEER Summary 1We investigated effects of declining plant species richness (S) on resistance to extremes in grassland communities. 2Synthesized model ecosystems of different S, grown outdoors in containers, were exposed to a stress peak combining heat and drought. The heat wave was induced experimentally by infrared irradiation in free air conditions. 3Before the heat wave, the more species-rich communities produced more biomass as a result of a large and positive complementarity effect that outweighed a small negative selection effect. 4Water use during the heat wave was likewise enhanced by S, which could not be attributed to dominance of ,water-wasting' species. Instead, water consumption at high S exceeded that expected from changes in community biomass and biomass composition. The observed enhancement of resource (water) acquisition under stress with increasing S therefore probably originated from complementarity. 5Despite enhanced water use in the more diverse communities, plant survival was significantly less, affecting all species alike. Physiological stress, recorded as photochemical efficiency of photosystem II electron transport, was significantly greater. Before the heat wave, the changes in biomass composition that coincided with increasing S did not favour species that would later prove intrinsically sensitive or insensitive. 6Complementarity in resource use for biomass production had a cost in terms of reduced survival under stress, despite the likelihood of complementarity in water acquisition during exposure. The greater loss of individuals from the more diverse grasslands suggests enhanced risk of local extinction. [source] Performance of High Arctic tundra plants improved during but deteriorated after exposure to a simulated extreme temperature eventGLOBAL CHANGE BIOLOGY, Issue 12 2005Fleur L. Marchand Abstract Arctic ecosystems are known to be extremely vulnerable to climate change. As the Intergovernmental Panel on Climate Change scenarios project extreme climate events to increase in frequency and severity, we exposed High Arctic tundra plots during 8 days in summer to a temperature rise of approximately 9°C, induced by infrared irradiation, followed by a recovery period. Increased plant growth rates during the heat wave, increased green cover at the end of the heat wave and higher chlorophyll concentrations of all four predominating species (Salix arctica Pall., Arctagrostis latifolia Griseb., Carex bigelowii Torr. ex Schwein and Polygonum viviparum L.) after the recovery period, indicated stimulation of vegetative growth. Improved plant performance during the heat wave was confirmed at plant level by higher leaf photochemical efficiency (Fv/Fm) and at ecosystem level by increased gross canopy photosynthesis. However, in the aftermath of the temperature extreme, the heated plants were more stressed than the unheated plants, probably because they acclimated to warmer conditions and experienced the return to (low) ambient as stressful. We also calculated the impact of the heat wave on the carbon balance of this tundra ecosystem. Below- and aboveground respiration were stimulated by the instantaneous warmer soil and canopy, respectively, outweighing the increased gross photosynthesis. As a result, during the heat wave, the heated plots were a smaller sink compared with their unheated counterparts, whereas afterwards the balance was not affected. If other High Arctic tundra ecosystems react similarly, more frequent extreme temperature events in a future climate may shift this biome towards a source. It is uncertain, however, whether these short-term effects will hold when C exchange rates acclimate to higher average temperatures. [source] Non-thermal cytocidal effect of infrared irradiation on cultured cancer cells using specialized deviceCANCER SCIENCE, Issue 6 2010Yohei Tanaka As infrared penetrates the skin, thermal effects of infrared irradiation on cancer cells have been investigated in the field of hyperthermia. We evaluated non-thermal effects of infrared irradiation using a specialized device (1100,18000 nm with filtering of wavelengths between 1400 and 1500 nm and contact cooling) on cancer cells. In in vitro study, five kinds of cultured cancer cell lines (MCF7 breast cancer, HeLa uterine cervical cancer, NUGC-4 gastric cancer, B16F0 melanoma, and MDA-MB435 melanoma) were irradiated using the infrared device, and then the cell proliferation activity was evaluated by 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay. Proliferation of all the cancer cell lines was significantly suppressed by infrared irradiation. Total infrared output appeared to be correlated with cell survival. Increased temperature during infrared irradiation appeared not to play a role in cell survival. The maximum temperature elevation in the wells after each shot in the 20 and 40 J/cm2 culture was 3.8°C and 6.9°C, respectively. In addition, we have shown that infrared irradiation significantly inhibited the tumor growth of MCF7 breast cancer transplanted in severe combined immunodeficiency mice and MDA-MB435 melanoma transplanted in nude mice in vivo. Significant differences between control and irradiated groups were observed in tumor volume and frequencies of TUNEL-positive and Ki-67-positive cells. These results indicate that infrared, independent of thermal energy, can induce cell killing of cancer cells. As this infrared irradiation schedule reduces discomfort and side effects, reaches the deep subcutaneous tissues, and facilitates repeated irradiations, it may have potential as an application for treating various forms of cancer. (Cancer Sci 2010) [source] | |||||||||||||