低能量氦氖激光照射对荷瘤小鼠T淋巴细胞增殖反应的影响

目的：本文研究低能量氦氖激光照射荷瘤小鼠,观察对荷瘤Ｔ淋巴细胞增殖反应的影响。结果：ＢＡＬＢ／Ｃ雄性小鼠腹腔接种Ｓ１８０接种后,进行激光照射小鼠内眼角,测定正常对照组、肿瘤对照组和７．３３、１１．００、１４．６７、２２．００Ｊ／ｃｍ＾２和２９．３３Ｊ／ｃｍ＾２五个剂量激光照射组小鼠的Ｔ淋巴细胞增殖反应,结果表明１１．００Ｊ／ｃｍ＾２、１４．６７Ｊ／ｃｍ＾２、２２．００Ｊ／ｃｍ＾２剂量的氦氖激光照射     

不同剂量的He—Ne激光对Raji细胞膜脂流动性的影响

本文采用荧光偏振法检测了不同剂量的Ｈｅ－Ｎｅ激光照射法对Ｒａｊｉ细胞膜流动性的影响,发现了０．０１Ｊ／ｃｍ＾２和０．５１Ｊ／ｃｍ＾２两剂量可使膜脂微粘度降低（Ｐ〈０．０５）。即其膜脂流动性升高;１．０Ｊ／ｃｍ＾２和２．０Ｊ／ｃｍ＾２的剂量脂微粘度无明显影响,即其膜流动性无明显化（Ｐ〉０．０５）,而６．０２Ｊ／ｃｍ＾２的剂量可使膜微粘度明显上升（Ｐ〈０．０５）。即其膜流动性明显下降。     

低强度HeNe激光辐照人体外周血对淋巴细胞染色体影响的研究

本文通过低强度Ｈｅ－Ｎｅ激光以能量密度分别为１４．３１Ｊ／ｃｍ＾２（辐照５’）、２８．６２Ｊ／ｃｍ＾２（辐照１０）、５７．２４Ｊ／ｃｍ＾２（辐照２０）１１４．５２Ｊ／ｃｍ＾２（辐照４０）燠夫体外周血后,检测其淋染色畸变率（ＣＡ）,激光照射血样（能量密度由低到高）未照射血样ＣＡ分别平均为４．２９‰、３．９６‰、３．８１‰、３．５９０‰、４．１９‰、Ｘ＾检测无显著差异,说明低强度的Ｈｅ－Ｎｅ激光辐照人     

不同剂量的He—Ne激光对Raji细胞膜表面SH的影响

本文以离体培养的Ｒａｊｉ细胞为材料,采用ＥＬＬＭＡＮ方法检测了不同剂量的Ｈｅ－Ｎｅ激光对Ｒａｊｉ细胞膜表面ＳＨ含量的影响。发现０．５Ｊ／ｃｍ＾２Ｈｅ－Ｎｅ激光能量可明显增加膜表面ＳＨ含量（Ｐ〈０．０５）。大于或小于此剂量的Ｈｅ－Ｎｅ激光对膜表面ＳＨ含量的影响均不明显（Ｐ〉０．０５）。提示０．５Ｊ／ｃｍ＾２的激光能量对膜有刺激作用。     

激光对尾草履虫分裂繁殖影响的研究

采用Ｈｅ－Ｎｅ激光辐照经单克隆培养的尾草履虫（Ｐａｒａｍｅｃｉｕｍｃａｕａｔｕｍ）无性繁殖系,观察并分析激光对尾草履虫分裂繁殖产生的影响,结果表明,在本实验条件下,当辐照的能量密度处于５０．９－１０１．９（Ｊ／ｃｍ＾２）范围内,激光对尾草履虫的分裂繁殖产生促进作用,当辐照的能量密度为１０１．９Ｊ／ｃｍ＾２时,草履虫分裂繁殖的个体平均数达最大值。草履虫对激光辐照有很大的耐受范围和很强的耐受能力。本实     

激光照射茶树花药培养及其过氧化物酶同工酶的分析

Ｈｅ－Ｎｅ和ＣＯ２激光对茶树花药培养的药裂率和出愈率的影响,既有促进作用,也有抑制作用。按出愈率和愈伤组织生长状况的序列：Ｈｅ－Ｎｅ：２０Ｊ／ｃｍ＾２〉ＣＫ〉Ｈｅ－Ｎｅ：３０Ｊ／ｃｍ＾２〉ＣＯ２：３５．４Ｊ／ｃｍ＾２。对Ｈｅ－Ｎｅ激光照射花药及其愈伤组织的过氧化物酶同工酶分析,主要表现在弱酶带的变化上,无规律差异。     

氦氖激光对甘蓝种子萌发的生物效应

本试验用氦氖激光辐照甘蓝种子,以探求对其生长发育的影响。结果表明,辐照剂量为１．０８Ｊ／ｃｍ￣２的处理对甘蓝种子萌发期间的一些生理生化指标均有促进作用,而剂量为２．０７Ｊ／ｃｍ￣２的处理却有抑制作用。     

低强度He-Ne激光辐照人体外周血对淋巴细胞染色体影响的研究

本文通过低强度 Ｈｅ Ｎｅ 激光以能量密度分别为 １４３１ Ｊ／ｃｍ ２ （辐照 ５′）、２８６２ Ｊ／ｃｍ ２ （辐照 １０′）、５７２４ Ｊ／ｃｍ ２ （辐照 ２０′）１１４５２ Ｊ／ｃｍ ２ （辐照 ４０′）照射人体外周血后,检测其淋巴细胞染色体畸变率（ Ｃ Ａ）,激光照射血样（能量密度由低到高）及未照射血样 Ｃ Ａ 分别平均为 ４２９‰、３９６‰、３８１‰、３５９‰、４１９‰, Ｘ２ 检验无显著差异（ Ｐ＞ ００５）,说明低强度的 Ｈｅ Ｎｅ 激光辐照人体细胞对细胞染色体无致畸变效应。而且随着能量密度的增大,染色体的畸变率有降低的趋势,因此认为是低强度的 Ｈｅ Ｎｅ 激光促使细胞内分子的相互作用和能量转换,从而使染色体损伤的修复增强,其机理有待于进一步的研究。     

激光诱导杨树花粉单倍体植株的研究

用Ｈｅ－Ｎｅ激光适宜剂量２０Ｊ．ｃｍ＾－２诱导杨树花药培养花粉单倍体植株及其无性系获得成功。     

弱激光对脂质体介导的血管平滑肌细胞基因转染的影响

本研究采用阳离子脂质体介导外源基因转染体外培养的兔血管平滑肌细胞（ＳＭＣ）,在基因转染过程中给予激光照射,用细胞化学染色方法测定基因转染阳性率。结果显示：用５１０．６ｎｍ激光于基因转染前,以功率密度１ｍｗ／ｃｍ２,能量密度２、４、６Ｊ／ｃｍ２和５ｍＷ／ｃｍ２,４、６Ｊ／ｃｍ２;及１０ｍＷ／ｃｍ２,２Ｊ／ｃｍ２进行照射均能显著提高基因转染率（ｐ＜０．０５）;于基因转染后即刻以功率密度１ｍＷ／ｃｍ２、能量密度２Ｊ／ｃｍ２和５ｍＷ／ｃｍ２、６Ｊ／ｃｍ２照射也能提高基因转染率（ｐ＜０．０５）。而用６２７．８ｎｍ激光照射对基因转染率无显著影响     

Molecular aspects of photodynamic therapy: low energy pre-sensitization of hypericin-loaded human endometrial carcinoma cells enhances photo-tolerance, alters gene expression and affects the cell cycle

Photosensitization of HEC1-B cells with a low concentration of hypericin and doses of light below 10 J/cm(2) caused cell death (apoptosis occurred mainly at doses between 2 and 5 J/cm(2), whereas necrosis prevailed above 6 J/cm(2)). However, pre-exposure of cells to innocuous irradiation (2 J/cm(2)) and successive challenge with a light dose that normally induced apoptosis (5 J/cm(2)) altered the expression of the proteins involved in the regulation of apoptosis, stress response and cell cycle. This change resulted in a significant increase in cell photo-tolerance.     

Cytogenetic effects of UV laser radiation with wavelengths of 248, 223 and 193 nm on mammalian cells

Ten hours after irradiation of mouse cornea with doses of 0.09 to 1.5 J/cm2 the incidence of cells with chromosome aberrations increased linearly with dose and amounted to 11.7% at 248 nm, 5.5% at 223 nm and 2.6% at 193 nm per 1 J/cm2. No induced chromosome aberrations occurred 72 hr following irradiation. Within the dose range from 3.0 to 18 J/cm2 the cytogenetic effect of radiation was less manifest than that with the doses mentioned above, the frequency of chromosome aberrations being independent of either wave length or radiation dose and amounted to 2.5 to 3.0%.     

Effects of UV-irradiation of carp sperm and its modification by caffeine

In connection with the development of UV-induced mutagenesis in carp, the effects of UV-irradiation of sperms have been studied in the range of doses 0.3-40 J/m2. The irradiation did not cause reduced fertilization ability and cleavage delay. Small doses of irradiation (0.6 J/m2) produced stimulating effect on embryo survival, the larvae yield decreasing and the amount of aberrant anaphases increasing, as the doses are increased. LD50 is 6.0 J/m2 for embryonal period of carp development, photoreactivation increases it up to 23.5 J/m2. Correlation between embryo viability and their resistance to UV has been found (r = +0.68 +/- 0.20). Modification of the effect of sperms irradiation with caffeine has been also studied. Strengthening of lethal and cytogenetic effects was only observed in case when embryos were placed in the caffeine solution, prior to onset of the first DNA replication in the male pronucleus. This may indicate the existence of caffeine-dependent prereplicative repair in carp embryos.     

Improvement of stored turkey semen quality as a result of He-Ne laser irradiation

Two experiments were carried out to evaluate the effects of He-Ne laser irradiation at various energy doses on the quality of stored turkey semen. Four semen pools were used in Experiment 1. Each pool was divided into 10 aliquots, nine of which were irradiated with energy doses ranging from 0.144 to 10.8 J/cm2 while the tenth one was not irradiated (control). Each sample was evaluated for motility immediately after irradiation, 24 and 48 h later. Energy doses ranging from 3.24 to 5.4 J/cm2 had higher (P <0.01) sperm motility index (SMI) value compared to the control and samples irradiated with lower and higher laser doses. The energy dose of 3.96 J/cm2 was selected for Experiment 2 to obtain further insight on its effects on turkey sperm preservation for up to 60 h. Each pool of four semen was divided into two aliquots: one represented the control and the other one was irradiated with He-Ne laser at an energy dose of 3.96 J/cm2. Each sample was evaluated for motility and viability immediately after irradiation and then at 12 h intervals up to 60 h. The cell energy charge was also measured by HPLC. Exposure to 3.96 J/cm2 increased the SMI and viability of turkey semen stored for 60 h compared to the control (P <0.05). The cell energy charge of irradiated samples was 200% higher than in the control. Laser irradiation increased the longevity of stored turkey spermatozoa, and might be a useful technique to enhance semen quality in long-term storage.     

Effect of copper vapor laser on the microrelief and ultrastructure of gastric mucosal glandulocytes

It was investigated the influence of low intensive irradiation by the copper++ vapor laser (lambda-510.6 nm) on the glandulocytes of gastric mucosa of 28 white rats. The doses of endogastric irradiation were 6.78, 20.34 and 33.90 J/cm2. It has been shown that after irradiation of gastric mucosa with the copper++ vapor laser the microrelief and ultrastructure of glandulocytes changes testified to stimulation of specific secret function. This changes took place under irradiation doses from 6.78 to 20.34 J/cm2. The doses exceeded 20.34 J/cm2 caused the alterations of the epitheliocytes. Thus it is necessary to take into account that during laser therapy of the ulcers with copper++ vapor laser, doses of 20.34 J/cm2 caused the alterative effect on the epitheliocytes.     

Photobiological and thermal effects of photoactivating UVA light doses on cell cultures.

While near-ultraviolet light has been widely used to photoactivate fluorophores and caged compounds in cells, little is known of the long-term biological effects of this light. UVA (315-400 nm) photoactivating light has been well characterized in short-term cell studies and is now being employed in higher doses to control longer-duration phenomena (e.g. gene expression). Annexin V-Cy5/propidium iodide apoptosis flow cytometry assays were used to determine responses of HeLa cells to doses of UVA light up to 23.85 J cm(-2). Cells seeded at low densities had higher percentages of apoptosis and necrosis and were also more susceptible to UVA damage than cells seeded at higher densities. The dose to induce apoptosis and death in 50% of the cells (dose(1/2)) was determined for two different commercially available UVA light sources: 7.6 J cm(-2) for the GreenSpot photocuring system and 2.52 J cm(-2) for the BlakRay lamp. All BlakRay doses tested had significant cellular responses, whereas no significant cellular responses were found for doses below 1.6 J cm(-2) from the GreenSpot light source. A temperature control and measurement system was used to determine direct heating from the UVA sources and also the effect that cooling cell cultures during photoexposure has on minimizing cell damage. Cooling during the BlakRay photoexposure significantly reduced the percentage of necrotic cells, but there was no significant difference for cooling during photoactivation with the GreenSpot. Differences in cell responses to similar UVA doses of different intensities suggest that photoduration should be considered along with total dose and thermal conditions in photoactivation studies.     

Dose-dependent metabolic response of mammary carcinoma to photodynamic therapy

The metabolic response of mammary carcinoma in the C3H mouse to photodynamic therapy (PDT) was measured using in vivo 31P nuclear magnetic resonance (31P-NMR) spectroscopy and pH microelectrodes. Twenty-four hours after administration of Photofrin II (12.5 mg/kg), the tumor was subjected to photoactivation using an argon dye laser. Optical treatment doses were 200, 400, and 600 J/cm2 and corresponded to the following tumor control doses: TCD10/30, TCD50/30, and TCD90/30, respectively. In vivo 31P-NMR spectra and pH micro-electrode measurements were obtained prior to treatment and at 4, 24, 48, and 72 h and 1 week post-treatment. The data revealed a significant (P less than 0.0002) alkalosis as indicated by the pH measured by NMR compared to pH measured by microelectrodes at all treatment levels and time points. Spectral differences between treatment groups were apparent as early as 4 h after treatment. The ratio of beta-nucleoside triphosphate to inorganic phosphate at 4 h after treatment was significantly (P less than 0.01) smaller for 600 J/cm2 treatment than for 200 J/cm2 treatment. At curative (600 J/cm2) levels, from 48 h on, no phosphate resonances were detected in the spectra. The pH measured by NMR transiently decreased from pretreatment levels after 200 and 400 J/cm2 treatment (P less than 0.002, P less than 0.009, respectively), while no change in pH from pretreatment values was found after 600 J/cm2 treatment. The data suggest that the early metabolic response of mammary carcinoma to PDT, as indicated by 31P-NMR spectroscopy, is dose dependent, and may be a sensitive indicator of biological outcome to treatment.     

氦氖激光对离体小鼠腹腔巨噬细胞功能的影响

为探索低功率激光照射治疗的机理,本实验用氦氖激光照射离体小白鼠腹腔巨噬细胞观察其吞噬鸡红细胞折功能。当照射１５分钟时,巨噬细胞蚕噬功能达到最大值,以后开始下降,照射至４０分时,巨噬细胞吞噬功能下降至对照组以下,出现抑制现象。     

氦氖激光对大鼠心肌超微结构、SOD和MDA影响的观察

为了解低强度氦氖激光对心肌细胞超微结构、超氧化物歧化酶（SOD）和丙二醛（MDA）的影响,采用2．87J／cm^2,7.17J/cm^2和28.66J/cm^2三种剂量氦氖激光照射大鼠心前区,电镜观察心肌超微结构,测定心肌组织SOD和MDA的含量。结果发现心肌线粒体有轻微损伤,心肌组织SOD含量在7．17J／cm^2剂量显著下降（P＜0．05）,而在28．66J／cm^2剂量显著升高（P＜0．05）,心肌组织MDA含量在7．17J／cm^2和28．66J／cm^2两种剂量下降有显著升高（P＜0．01）,在2．87J／cm^2剂量,心肌组织SOD和MDA含量均无显著变化（P＜0．05）。结果提示心肌SOD含量和脂质过氧化随不同的激光剂量而变化。     

578.2 nm激光照射对兔视网膜的损伤效应研究

研究578.2 nm激光照射对兔视网膜的作用特点,以新西兰白兔5只10眼为实验对象,铜蒸汽激光(578.2 nm)通过裂隙灯照射兔视网膜后极部,照射时间为100 s,光斑直径为2 mm,照射剂量分别为60 J/cm2、80 J/cm2、100 J/cm2、120 J/cm2、160 J/cm2、200 J/cm2,每组4个光斑。照后1 h及24 h进行眼底照相及光镜观察。照光后可见,随激光功率密度的增加,兔视网膜的损伤也逐渐加重,并且照后24 h的损伤要重于照后1h。80 J/cm2和60 J/cm2在照后1 h和24 h均未发现明显改变。578.2 nm激光照射白兔后的主要病理学改变位于脉络膜。因此,以578.2 nm激光作为光动力治疗眼底疾病的光源时,照射剂量不宜超过80 J/cm2。