川崎 晃一
Kyushu University
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Nippon Eiyo Shokuryo Gakkaishi | 1999
関 英治; 川崎 晃一; 吉田 真弓; 筬島 克裕; 玉屋 圭; 松井 利郎; 筬島 豊
J Jpn Soc Nutr Food Sci 52: 271-277 (1999) The antihypertensive effect of peptides (Y-2) derived from sardine, valyl-tyrosine and -mixture (MIX) of four dipeptides having angiotensin converting enzyme inhibitory activity was studied in spontaneously hypertensive rats (SHR) .1) Single oral administration of Y-2, valy1-tyrosine and MIX lowered the systolic blood pressure in SHR, and its minimum effective doses were 10, 1, and 10 mg/ kg, respectively. These effects lasted for 8 h after administration. The hypotensive potency of valy1-tyrosine was greater than those of Y-2 and MIX. Valy1-tyrosine (1 and 10 mg/kg) lowered the blood pressure dose-dependently. 2) When 1000, 10, and 10 mg of Y-2, valy1-tyrosine and MIX, respectively, were administered orally to the SHR twice a day for 10 consecutive days, any of the regimens decreased systolic blood pressure significantly, and the decrement of systolic blood pressure continued for 5 days thereafter. These results indicate that either Y-2, valy1-tyrosine or MIX can exert a potent and long-lasting antihypertensive effect in SHR.
Folia Endocrinologica Japonica | 1984
川崎 晃一; 中牟田 澄子; 村谷 博美; 尾前 照雄
A method of radioimmunoassay for urinary aldosterone excretion (AER) using 125I-labeled ligand [ALDOCTK-125KIT] is described. The sensitivity, specificity, reproducibility and accuracy of this method were compared with the 3H-RIA method previously reported. Since the extraction method using ALDOCTK-125KIT was considered to be preferable to the direct method, the former method was applied to the present study. An excellent correlation was found between the values determined by the 3H-RIA method and the extraction method (r = 0.935, p less than 0.001, Y = 0.89X + 0.80, n = 146). The within-assay and the between-assay coefficient of variation was 7.7--15.0% and 9.7--12.2%, respectively. As a clinical application, the circadian variation of AER was investigated in 5 control subjects and groups of essential hypertension (EHT), primary aldosteronism (PA), chronic glomerulonephritis (CGN) and Cushings syndrome, each of which consisted of 5 patients, all of which had serum creatinine concentrations of less than 1.2 mg/dl. Under a control diet containing 10 g of salt per day, urine was collected in 4-hour pools starting at 8:00 for the ensuing 24 hours, and AER was determined by means of both 3H-RIA and the extraction method. The difference of the values between the peak and the nadir in each subject was statistically significant, and marked and identical circadian variations of AER with the peak and the nadir at the period of 4:00 to 12:00 and 20:00 to 4:00 were observed in the control, EHT, PA and CGN groups. In the Cushing group, however, the circadian variation of AER was different from the other 4 groups: the peak and the nadir of AER occurred at the period of 20:00 to 24:00 and 4:00 to 8:00, respectively. The circadian variation of AER became more obvious in all groups including the Cushing, when each value was expressed in the percentage of the mean. AER under the control diet was 9.38 +/- 2.04 micrograms/day in the control subjects. In PA and CGN, AER was significantly higher, and in the Cushing group, it was significantly lower than that observed in the control. However, no difference was found in AER between the control and EHT. AERs in both 4-hour and 24-hour urine specimens measured by ALDOCTK-125KIT were consistent with those by the 3H-RIA method.
Journal of Health Science | 1986
川崎 晃一; Kawasaki Terukazu; 上園 慶子; Uezono Keiko; Utsunomiya Hiroko; 宇都宮 弘子; Imamura Kyoko; 今村 京子; Kikkawa Kazutoshi; 吉川 和利; 上野 道雄; Ueno Michio; 藤島 正敏; Fujishima Masatoshi; カワサキ テルカズ; ウエゾノ ケイコ; ウツノミヤ ヒロコ; イマムラ キョウコ; キッカワ カズトシ; ウエノ ミチオ; フジシマ マサトシ
Journal of Health Science | 1984
川崎 晃一; Kawasaki Terukazu; Uezono Keiko; 上園 慶子; Ueno Michio; 上野 道雄; Kikkawa Kazutoshi; 吉川 和利; Komuro Toshie; 小室 史恵; Nakamuta Sumiko; 中牟田 澄子; 川副 信行; Kawazoe Nobuyuki; 村谷 博美; Muratani Hiromi; Omae Teruo; 尾前 照雄; カワサキ テルカズ; ウエゾノ ケイコ; ウエノ ミチオ; キッカワ カズトシ; コムロ トシエ; ナカムタ スミコ; カワゾエ ノブユキ; ムラタニ ヒロミ; オマエ テルオ
Nippon Eiyo Shokuryo Gakkaishi | 1998
伊藤 和枝; 川崎 晃一
Journal of Health Science | 1988
Kawasaki Terukazu; 川崎 晃一; 上園 慶子; Uezono Keiko; 伊藤 和枝; Itoh Kazue; Ueno Michio; 上野 道雄; 藤島 正敏; Fujishima Masatoshi; カワサキ テルカズ; ウエゾノ ケイコ; イトウ カズエ; ウエノ ミチオ; フジシマ マサトシ
Journal of Health Science | 1990
Uezono Keiko; 上園 慶子; 川崎 晃一; Kawasaki Terukazu; 大柿 哲朗; Ogaki Tetsuro; Itoh Kazue; 伊藤 和枝; 小林 茂; Kobayashi Shigeru; 吉水 浩; Yoshimizu Yutaka; 大坂 哲郎; Osaka Tetsuro; 中島 弘二; Nakashima Koji; Dhungel Sanjib; P Acharya Gopal; Sharma Sashi; Shrma Sashi; Upadhya Prakash; Ogata Michihiko; 緒方 道音; ウエゾノ ケイコ; カワサキ テルカズ; オオガキ テツロウ; イトウ カズエ; コバヤシ シゲル; ヨシミズ ユタカ; オオサカ テツロウ
Journal of Health Science | 1998
Kawasaki Terukazu; 川崎 晃一; 伊藤 和枝; Ito Kazue; 大柿 哲朗; Ogaki Tetsuro; 吉水 浩; 小林 茂; 上園 慶子; K Ghimire Pradeep; Sharma Sashi; P Acharya Gopal; Itoh Kazue; Yoshimizu Yutaka; Kobayashi Shigeru; Uezono Keiko; カワサキ テルカズ; イトウ カズエ; オオガキ テツロウ; ヨシミズ ユタカ; コバヤシ シゲル; ウエゾノ ケイコ
Folia Endocrinologica Japonica | 1980
上園 慶子; 川崎 晃一; 上野 道雄; 中牟田 澄子; 尾前 照雄
Journal of Health Science | 1993
伊藤 和枝; Itoh Kazue; Kawasaki Terukazu; 川崎 晃一; 大柿 哲朗; Ogaki Tetsuro; Yoshimizu Yutaka; 吉水 浩; Funatsu Suehiro; 船津 末弘; Shakya Nani Shova; Shankya Nani Shova; K Ghimire Pradeep; P Acharya Gopal; イトウ カズエ; カワサキ テルカズ; オオガキ テツロウ; ヨシミズ ユタカ; フナツ スエヒロ