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The present state of knowledge on the importance of calcium ions and inositol phospholipids in the metabolic changes associated with early stages of platelet activation is outlined, with stress laid in the biochemical mechanisms of intracellular rise of calcium ion concentration. The metabolism of inositol phospholipids is briefly discussed stressing the importance of the metabolites of these phospholipids--1,2-diacylglycerol and 1,4,5-inositol triphosphate which are of key importance in the transfer of information between platelet membrane and intracellular structures.  相似文献   
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Zusammenfassung Die Antirheumatica Prednisolon, Phenylbutazon, Resochin, Natriumgentisinat und Natriumsalicylat hemmen die durch hämolytischen Hammelblutamboceptor und Komplement bewirkte Hammelbluthämolyse.Diese Wirkung der Antirheumatica kommt durch eine Inaktivierung des Amboceptors (Antikörpers) zustande. Das Komplement und die Hammelblutkörperchen werden bei diesen Versuchen von den Antirheumatica nicht beeinflußt.Es besteht eine strenge quantitative Beziehung zwischen Amboceptorkonzentration und Antirheumaticumkonzentration. Je höher die Konzentration des Amboceptors ist, um so stärkere Antirheumaticakonzentrationen sind zu seiner Inaktivierung nötig.Bezogen auf die wirksamen molaren Endkonzentrationen sind Prednisolon 8,5, Phenylbutazon 6,5, Resochin 5,0 und Gentisinsäure 1,5mal stärker wirksam als Salicylsäure.Wird der Amboceptor mit bestimmten Konzentrationen von Phenylbutazon, Natriumgentisinat oder Natriumsalicylat vorbehandelt, so kann mit diesem Amboceptor der Forssman-Schock (invers-anaphylaktischer Schock) nicht mehr beim Meerschweinchen ausgelöst werden. Phenylbutazon und Natriumgentisinat sind dabei etwa gleichstark wirksam, während Natriumsalicylat wesentlich schwächer wirkt als die beiden anderen Substanzen.  相似文献   
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COPD is the most frequent chronic lung disease in Poland. The disease is however under-diagnosed, especially at the early stages. The aim of the study was to assess the efficacy of spirometric screening for COPD in middle aged smokers. Informations on causes and symptoms of COPD were disseminated in mass media in 14 large cities. Subject aged over 39 and with smoking history of > 10 packyears were invited for a free spirometry in local chest clinic. However, everyone attending had the spirometry performed. Spirometry was performed according to ATS recommendations. Airway obstruction (AO) was diagnosed when FEV1/FVC < 85% of N and categorised as mild (FEV1 > 70% of N), moderate (FEV1 50-69% of N) or severe (FEV1 < 50% of N). Spirometry was accompanied by an antismoking advice. RESULTS: 12.781 subjects were screened (mean age 52 +/- 12 years, 57% males). In 8.269 subjects who complied with inclusion criteria AO was diagnosed in 29.8% (mild in 10.9%, moderate in 12% and severe in 6.9%). In smokers < 40 years of age and a history of < 10 packyears AO was found in 8.8% (mild in 6.0%, moderate in 1.8% and severe in 1.0%). CONCLUSION: Mass spirometry is an effective and easy method for early detection of COPD.  相似文献   
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We investigated immune responses against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) among a group of convalescent, potential blood donors in Germany who had PCR-confirmed SARS-CoV-2 infection. Sixty days after onset of symptoms, 13/78 (17%) study participants had borderline or negative results to an ELISA detecting IgG against the S1 protein of SARS-CoV-2. We analyzed participants with PCR-confirmed infection who had strong antibody responses (ratio >3) as positive controls and participants without symptoms of SARS-CoV-2 infection and without household contact with infected patients as negative controls. Using interferon-γ ELISpot, we observed that 78% of PCR-positive volunteers with undetectable antibodies showed T cell immunity against SARS-CoV-2. We observed a similar frequency (80%) of T-cell immunity in convalescent donors with strong antibody responses but did not detect immunity in negative controls. We concluded that, in convalescent patients with undetectable SARS-CoV-2 IgG, immunity may be mediated through T cells.  相似文献   
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Summary Canine distemper, a naturally occurring viral disease of dogs which often terminates in parainfectious demyelination, was used as a model to study the role of acid proteinase, neutral proteinase and beta-glucuronidase in demyelination. These enzymes were higher in cerebella of dogs with distemper-associated demyelination than in age-matched controls. The highest elevations corresponded with the most severely demyelinated cerebella. The source of the increased enzymes activities was apparently unrelated to the lymphocytes present in areas of demyelination.The direct effect of distemper virus and serum on these enzymes was tested in canine glial monolayers. Virus infection resulted in lower enzyme activities in cells concomitant with the appearance of cellular lesions. There was a relative increase of beta glucuronidase activity in the media suggesting that distemper virus released pre-formed lysosomal enzymes. Serum which was obtained from dogs with distemper-associated demyelination and had previously demyelinated cerebellar explants, also decreased activities of all 3 enzymesin vitro.The 3 enzymes were measured in gerbil brains at various time intervals following unilateral cerebral infarction to determine if processes other than demyelination also caused these enzymes to be increased. Uncomplicated ischemic necrosis (24 h post infarction) did not alter the activities of these enzymes. Invasion of macrophages to ingest and digest necrotic tissue 10 days after infarction resulted in greatly increased acid proteinase and beta-glucuronidase, but unchanged neutral proteinase, activities.It was concluded that the increased activities of acid proteinase and beta-glucuronidase in demyelinated tissue probably are derived from macrophages ingesting damaged tissue. Neutral proteinase may be more specifically involved in the demyelinating process since this is partially located within myelin and can degrade the basic protein of myelin.Supported in part by Research grant Nos. GM 1052 and Al-09022 from National Institutes of Health Service, U.S. Public Health Service.  相似文献   
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Altered calcium homeostasis has been demonstrated in human spinal cord motor axon terminals of ALS patients, in spinal motor neurons of mutant SOD transgenic mice and following injection of ALS immunoglobulins. In all three paradigms oculomotor neurons are relatively spared. To explore mechanisms of selective resistance, we applied similar calcium localization techniques to terminals of oculomotor neurons in the two animal models. In both cases large vacuoles, which connect with the extracellular space, accumulated the majority of intracellular calcium, while terminals of vulnerable neurons (e.g. innervating interosseus muscle), which possess no such vacuoles, displayed evenly distributed calcium. These relatively unique membrane enveloped structures may permit neurons to control their cytoplasmic Ca2+ concentration and contribute to selective resistance.  相似文献   
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