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  • 1
    ISSN: 1432-0533
    Keywords: Key words Amyloid β-peptide ; Alzheimer’s disease ; Amyloid deposits ; Tissue transglutaminase ; Protein polymerization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The brain of Alzheimer’s disease patients contains deposits of the 39–42-amino acid (∼ 4 kDa) amyloid β-peptide, which is derived from the β-amyloid precursor protein. These pathological deposits have been shown to consist in part of insoluble 8- and 16-kDa aggregates of the amyloid β-peptide. This report confirms that the amyloid β-peptide is a substrate for tissue transglutaminase (TGase) and demonstrates that human brain preparations from Alzheimer’s disease patients and control patients form cross-linked dimers from added iodinated amyloid β-peptide. Immunohistochemical staining for TGase revealed its presence in tissue sections and isolated amyloid plaque cores obtained from brains of patients diagnosed as having Alzheimer’s disease. These results provide evidence that the previously described insoluble amyloid deposits in Alzheimer’s disease may involve TGase-mediated cross-linked amyloid β-peptide polymers, and suggest a potential role for TGase in the pathogenesis of this disease.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 21 (1982), S. 491-497 
    ISSN: 1432-1041
    Keywords: heparin ; anticoagulant effect ; serine protease inhibitors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The significance of baseline coagulation times and plasma concentrations of serine protease inhibitors as determinants of the relationship between heparin activity and its anticoagulant effect has been investigated in vitro. Citrated plasma was prepared from blood obtained from 20 normal subjects, and heparin added to yield concentrations ranging from 0.05 to 1.5 units/ml. The anticoagulant effect was determined by the activated partial thromboplastin time (APTT) and thrombin time (TT). An excellent linear relationship was observed between the natural logarithms (ln) of the coagulation times and heparin activity. Baseline APTT values ranged from 28.4 to 59.7 s and the slope values for the ln APTT vs heparin curves ranged from 1.488 to 3.427 ml/unit. Similar range was observed in the slope values for the ln TT vs heparin curves. There was a highly significant positive correlation between the ln APTT vs heparin slope values and the baseline APTT values (r: 0.905; p〈0.001). There was also a weak but statistically significant positive correlation between plasma concentrations of α2 macroglobulin and baseline APTT values (0.02〉p〉0.01) and slope values of the ln APTT vs heparin curves (0.02〉p〉0.01). Furthermore, there was a statistically significant positive correlation between plasma concentrations of α1 antitrypsin and baseline TT values (0.05〉p〉0.02) and slope values of the ln TT vs heparin curves (0.02〉p〉0.01). Neither baseline APTT and TT values nor slope values of the ln APTT and TT vs heparin curves were statistically significantly related to plasma concentrations of antithrombin III, fibrinogen, or α1 acid glycoprotein. This study has demonstrated that baseline APTT is a major determinant of the anticoagulant response to heparin in vitro, as determined by that same coagulation test, and it illustrates that there is a wide intersubject variation in the anticoagulant response to heparin in vitro.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 54 (1998), S. 243-247 
    ISSN: 1432-1041
    Keywords: Key words Eptastigmine ; Food ; Absorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Abstract Objective: The aim of the study was to evaluate the effects of food on the rate and extent of eptastigmine absorption in healthy volunteers. Methods: The study was carried out according to a double-blind, randomized, placebo-controlled, three-way cross-over design. On three separate occasions, six young subjects received 30 mg eptastigmine after a 12-h overnight fast (reference treatment), 30 mg eptastigmine 15 min after a standard breakfast (test treatment) and placebo 15 min after a standard breakfast (control treatment). Acetylcholinesterase activity in red blood cells was assayed 24 h after drug administration as a biological marker of eptastigmine plasma concentrations. Results: Mean maximum acetylcholinesterase inhibition (Imax) was 39.9% after eptastigmine without food and 33.1% after eptastigmine with food. Maximum inhibitions occurred at 4.75 h and 4.88 h after eptastigmine without and with food, respectively. Areas under the curve of acetylcholinesterase per cent inhibition from 0 to 8 h after drug administration (AUC0–8) were 198% h after eptastigmine without food and 124% h after eptastigmine with food. Ninety per cent confidence intervals of test/reference ratios for AUC0–8 and Imax exceeded the 0.80 to 1.20 limits, thus indicating that the two eptastigmine treatments cannot be considered bioequivalent. Mild and transient adverse events were recorded in three subjects receiving eptastigmine without food, one subject receiving eptastigmine with food and one subject receiving placebo. Conclusions: The ingestion of food significantly reduces the bioavailability of eptastigmine estimated by the assay of red blood cell acetylcholinesterase activity.
    Type of Medium: Electronic Resource
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