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  • 2000-2004  (1)
  • 1985-1989  (1)
  • Biochemistry and Biotechnology  (1)
  • Keywords: Calcium; Immunological activity; Intravascular low level laser irradiation (ILLLI); Low level laser irradiation (LLLI); Lymphocyte; Neuroglia  (1)
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  • 1
    ISSN: 1435-604X
    Keywords: Keywords: Calcium; Immunological activity; Intravascular low level laser irradiation (ILLLI); Low level laser irradiation (LLLI); Lymphocyte; Neuroglia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Physics , Technology
    Notes: Abstract . The purpose of this study was to determine the wavelength-response effects of low level laser irradiation (LLLI) on immunocompetence of mice in vivo and intracellular free calcium ([Ca2+]i) in human lymphocytes and cultured cortical neurogliocytes (CCN) in vitro. Mice were first immune compromised by cyclophosphamide (CTX) injection, and the immunological activities including the production of interleukin 2 (IL-2), the murine mixed lymphocyte reaction (MLR), the mitogenic response of murine thymocytes (MRT), the proliferation of murine bone marrow cells (BMC) and the natural killer (NK) cells activity, were investigated after intravascular low level laser irradiation (ILLLI) (1 mW, 1.1×104 J/cm2) at wavelengths of 532 nm, 632.8 nm, 650 nm and 1520 nm, respectively. In addition, using Ca2+ sensitive indicator Fura-2 AM with the Spex AR-CM-MIC cation measurement system ([Ca2+]i) in single human lymphocytes and CCN were measured after LLLI (7.5 J/cm2) at wavelengths of 532 nm, 632.8 nm, 650 nm, 810 nm and 1300 nm, respectively. Results showed that the ILLLI at wavelengths of 532 nm, 632.8 nm and 650 nm, produced a significant increase in the proliferation of BMC and the NK activity. The production of IL-2 was greatly promoted after irradiation at 632.8 nm and 650 nm. After irradiation at 532 nm and 650 nm, the murine MLR was evidently enhanced, and MRT was dramatically increased only after irradiation at 632.8 nm. In contrast, no significant effects were found on the above mentioned indexes by irradiation at 1520 nm in comparison to the control. In addition, [Ca2+]i in single human lymphocytes and CCN were increased after LLLI at wavelengths of 532 nm, 632.8 nm and 650 nm, respectively, whereas they were not significantly affected by the wavelengths of 810 nm and 1300 nm. Our results indicated that LLLI could induce significant and different effects on the immunological activities of the mice and cause an increase in [Ca2+]i in single human lymphocytes and CCN. Furthermore, these effects are dependent on the wavelengths, for example, more positive effects produced by the wavelengths of 532 nm, 632.8 nm and 652 nm than those produced by the wavelengths of 810 nm, 1300 nm and 1520 nm.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0952-3499
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The mobility of purified μ opioid binding protein in SDS-polyacrylamide gek electrophoresis is sensitive to the presence of reducing agents. In the presence of increasing concentrations of DTT the apparent molecular weight increases in a stepwise fashion from 53 kDa to 65 kDa. This reduction in mobility is attributed to the successive breakage of disulfide bridges, resulting in an increasingly asymmetric molecule. Treatment of cell membranes from various brain areas with reducing agents, such as DTT, produced a concentration-dependent inhibition of opioid binding. Sensitivity to DTT inhibition varied between receptor types, μ 〉 δ ≫ κ. For μ receptors, agonist binding was considerably more sensitive to DTT than antagonist binding. Inhibition by DTT is readily reversible and is unaffected by Na+ and/or Mg2+ ions. Reversibility may be partially prevented by the inclusion of a low concentration of a reducing reagent such as glutathione which does not inhibit binding but blocks reformation of disulfide bonds. Scatchard analysis of saturation data shows that DTT causes a pronounced decrease in binding affinity with little effect on receptor number. It is suggested that disulfide bonds are essential for ligand binding and that cleavage of one or more of these bonds may play a role in opioid receptor activation by agonists.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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