The Japanese Journal of Nephrology
Online ISSN : 1884-0728
Print ISSN : 0385-2385
ISSN-L : 0385-2385
Volume 17, Issue 4
Displaying 1-13 of 13 articles from this issue
  • Effects of Artron, Clofibrate and Intralipid on plasma lipids, postheparin lipolytic activity (PHLA) and immunoreactive insulin (IRI)
    M. Tsuchiya, J. Kawamura
    1975 Volume 17 Issue 4 Pages 195-207
    Published: April 30, 1975
    Released on J-STAGE: March 01, 2011
    JOURNAL FREE ACCESS
    Artron and clofibrate, which are effective in lowering plasma lipids, and intralipid, which is have an effect of fat load, were administrated to 15 patients undergoing maintenance hemodialysis with 3 months intervals of each drug and plasma lipids, PHLA and IRI were examined. 1) Those parients were stable biochemically by 18-24 hours hemodialysis a week and showed hypertriglyceridemia, increased free fatty acids (FFA), hypocholesterolemia, low level of PHLA and hyperinsulinemia before commencing medications. This kind of hyperlipidemia (high triglyceride, high FFA and low cholesterol) does not belong to the classification of Fredrickson. 2) The administration of artron (3 tablets daily for 56 days) resulted in a statistically significa-nt reduction of total cholesterol. IRI was also elevated by this drug. However, other plasma lipid fractions (β-lipoprotein, phospholipid, FFA) and PHLA were not altered. 3) The administration of clofibrate (750 mg daily for 28 days) resulted in a statistically signifi-cant reductions in total cholesterol, triglyceride and β-lipoprotein. However, there were no effects on phospholipid, FFA, PHLA and IRI. 4) By the fat load (500 ml of intralipid intravenously), total cholesterol, triglyceride and FFA were elevated to statistically significant levels after 8 hours with continuously high levels after 21 hours. Phospholipid, β-lipoprotein and IRI were not altered. It is in interest that PHLA was elev-ated to a statistically significant level after 8 hours and showed a still high level after 21 hours. If intralipid was loaded on the day of hemodialysis, total cholesterol, triglyceride and FFA also incre-ased to a statistically significant levels with lesser extent. 5) From this study, pathogenesis of hyperlipidemia, especially of triglyceride and FFA, was not completely elucidated. PHLA was continously low through the course of chronic hemodialysis and was not altered by drugs which lowered plasma level of triglyceride. It is in interest that the exog-enous elevation of plasma levels of triglyceride and FFA associated the elevation of PHLA. It is assumed that there are several factors which produce abnormalities of lipid metabolism in patients with intermittent hemodialysis. (I) High level of plasma insulin does not facilitate triglyceride synthesis in liver in one to one fashion, but hyperinsulinemia favors this pathway through the longterm hemodialysis. (II) High chlorie diet among patients with chronic hemodialysis resulted in increased utilization of FFA as a calorie source. Metabolic rate of FFA increases in association with increased FFA synthesis, and resynthesis of triglyceride from FFA will probably occur. (III) The possible synthesis mechanism of new acids and there after glycerides, from the exce-ssive amount of glucose and acetate absorbed through the dialysis membrane, should be considered. (IV) Large dosis of heparin is used generally at every hemodialysis and hemodialysis patient may obtain the low responsiveness to exogenous heparin. This leads to low PHLA and delayed clearing of triglyceride from blood.
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  • Toshihiko Nagasawa, Seiichi Shibata
    1975 Volume 17 Issue 4 Pages 209-214
    Published: April 30, 1975
    Released on J-STAGE: July 04, 2011
    JOURNAL FREE ACCESS
    Vascular lesions of small blood vessels in biopsied kidney tissues from 65 patients with SLE under long term steroid treatment were studied by light microscopy and imniunof luorescence. The intimal thickening with proliferation of elastic fibers of intralobular arteries was found in 9 cases, in whom 8 had proteinuria at the time of biopsy. In one case without proteinuria, fibrinoid degeneration was found in arterioles. Necrotizing angitis frequently observed in autopsied kidney of SLE was found in no cases. Clinical symptoms and courses of these patients were similar to those without vascular lesions. The thickening of basement membrane in addition to the proliferative changes was more prominent in these patients than those without vascular changes. All these patients showed granular deposits of IgG and/or β-1C globulin in GBM and/or mesangium. In small blood vessels, however, granular deposits were demonstrated in only one case. These results suggested that we should pay particular attention to such vascular lesions as well as glomerular lesions, when we interpret the light microscopy of kindney biopsies in patients with SLE under the long term control by steroids.
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  • J. Chung
    1975 Volume 17 Issue 4 Pages 215-217
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
    JOURNAL FREE ACCESS
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  • [in Japanese]
    1975 Volume 17 Issue 4 Pages 218-229
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
    JOURNAL FREE ACCESS
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  • [in Japanese]
    1975 Volume 17 Issue 4 Pages 230-236
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
    JOURNAL FREE ACCESS
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  • Kazunari Iidaka, Shigeru Sohtome, Toshiaki Serizawa
    1975 Volume 17 Issue 4 Pages 237-242
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
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  • [in Japanese], [in Japanese]
    1975 Volume 17 Issue 4 Pages 243-248
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
    JOURNAL FREE ACCESS
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  • Nobuyuki Yoshizawa
    1975 Volume 17 Issue 4 Pages 249-261
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
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  • Teruo WATANABE, Hideaki ARIHIRO
    1975 Volume 17 Issue 4 Pages 262-273
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
    JOURNAL FREE ACCESS
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  • [in Japanese]
    1975 Volume 17 Issue 4 Pages 274-275
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
    JOURNAL FREE ACCESS
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  • [in Japanese]
    1975 Volume 17 Issue 4 Pages 276-282
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
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  • [in Japanese]
    1975 Volume 17 Issue 4 Pages 283-286
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
    JOURNAL FREE ACCESS
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  • Itaru Kihara
    1975 Volume 17 Issue 4 Pages 287-291
    Published: April 30, 1975
    Released on J-STAGE: July 05, 2010
    JOURNAL FREE ACCESS
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