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  • Articles: DFG German National Licenses  (3)
  • 2000-2004  (3)
  • Cilazapril  (1)
  • Cross reactive material-positive  (1)
  • Key words Breast cancer  (1)
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  • Articles: DFG German National Licenses  (3)
Material
Years
  • 2000-2004  (3)
Year
  • 1
    ISSN: 1437-7799
    Keywords: Key words Nitric oxide ; NG-nitro-L-arginine ; Doxazosin ; Cilazapril
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background. We aimed to elucidate the involvement of the renin-angiotensin system (RAS) and sympathetic nervous system in hypertension induced by the long-term inhibition of nitric oxide (NO) production. Methods. We compared the effects of 9-week treatment with an angiotensin-converting enzyme inhibitor (ACEI), cilazapril (10 mg/kg per day), to that with an α1-adrenoceptor antagonist, doxazosin (10 mg/kg per day), on systemic blood pressure and renal histological changes in Sprague-Dawley rats continuously treated with oral NG-nitro-L-arginine (L-NA). Results. L-NA induced renal damage associated with a significant fall in urinary nitrate and nitrite (NOx) excretion and a significant rise in systolic blood pressure. Although cilazapril and doxazosin restored urinary NOx to a similar level, only cilazapril treatment significantly suppressed the hypertensive effect of L-NA. Urinary protein excretion in L-NA-treated rats was also significantly reduced by cilazapril treatment. Histologically, treatment with cilazapril, but not doxazosin, significantly inhibited the glomerular injury of mesangial expansion and glomerular sclerosis induced by L-NA treatment. Furthermore, cilazapril significantly reduced urinary aldosterone level. Conclusion. Our findings indicate that the hypertension and hypertensive glomerular injury induced by long-term L-NA treatment were abrogated by an ACEI but not by an α1-adrenoceptor antagonist, and that the fall in high blood pressure induced by treatment with the ACEI was independent of urinary NOx excretion in this model.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1437-7772
    Keywords: Key words Breast cancer ; Hematogenous recurrence ; PDGF expression of primary tumor ; Survival outcome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background. Many recent studies have found that several angiogenic factors play an important role in primary and metastatic tumor growth. Platelet-derived growth factor (PDGF) is known to induce angiogenesis. In this study, we investigated whether tumor PDGF can reliably predict metastatic potential and survival benefit in patients with breast cancer. Methods. Histoimmunological analysis with two isoforms of PDGF, PDGF-AA and PDGF-BB, was performed on formalin-fixed, paraffin-embedded tissue. This analysis was performed in 83 patients with breast cancer; 30 with hematogenous recurrence, 13 with locoregional recurrence, and 40 surviving without recurrence. Results. Of the 30 patients with hematogenous recurrence, 13 (43.3%) showed PDGF-AA expression [PDGF-AA(+) group] and the remaining 17 (56.7%) showed no expres-sion of tumor PDGF-AA [PDGF-AA(−) group]. In the locoregional recurrence group, 1 patient (7.7%) showed PDGF-AA expression, and 2 of the 40 patients surviving without recurrence (5%) showed PDGF-AA expression in the primary tumor tissue. In contrast, PDGF-BB expression was observed in all 43 patients with recurrence and in 37 of the 40 patients surviving without recurrence. The PDGF-AA(+) and locoregional recurrence groups had almost the same period to recurrence after surgery (25.2 ± 18.5 months and 24.0 ± 11.3 months, respectively), whereas this period in the PDGF-AA(−) group was significantly longer (P 〈 0.0489 and P 〈 0.0400, respectively) than that of these other two groups. The 2-, 5-, and 8-year survival rates for the PDGF-AA(−) group were 70.6%, 47.1%, and 35.3%, respectively, whereas those for the PDGF-AA(+) group were 61.5%, 23.1%, and 15.4%, respectively; those for the locoregional recurrence group were 76.9%, 23.1%, and 7.7%, respectively. The survival rate for the PDGF-AA(−) group tended to be better (P = 0.0907) than that for the PDGF-AA(+) group, and showed no difference (P = 0.148) from that of the locoregional recurrence group. Conclusion. The data on PDGF-BB expression indicate that PDGF-BB is largely concerned with primary tumor growth and is not related to hematogenous metastasis. In contrast, PDGF-AA expression seems to be linked with hematogenous metastasis.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1437-7799
    Keywords: Key words IgA nephropathy ; Factor XI deficiency ; Cross reactive material-positive ; Coagulation nephropathy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A 20-year-old man presented with proteinuria of increasing intensity, and persistent microhematuria. His renal biopsy findings were compatible with the diagnosis of IgA nephropathy, with diffusely increased mesangial matrix in the glomeruli shown on light microscopy and granular IgA deposition in the mesangium shown on immunofluorescence microscopy. Although his bleeding time and platelet counts were normal, he had a prolonged activated partial thromboplastin time (APTT). Coagulation studies showed that factor XI activity was decreased, to 39%. We immunoblotted plasma samples obtained from the patient and from one normal individual with polyclonal anti-human factor XI, and demonstrated that the factor XI antigen level of the patient was comparable to that of the normal control. A family study showed that the father of the patient had a similar coagulation abnormality, with normal factor XI antigen level. These findings suggest that the patient has a congenital factor XI abnormality with cross-reactive material positivity complicating IgA nephropathy. The findings imply the possible importance of clotting disorders in the pathogenesis and/or development of IgA nephropathy.
    Type of Medium: Electronic Resource
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