Reduced glutathione (GSH)의 組織細胞內로의 移動樣相의 一端을 알고져 마우스 大腦의 切片을 作成하고 이것을 1mM, 2mM 및 3mM의 GSH溶液中에 둔後 4C, 25C 및 37C의 溫度下에서 incubate 하고 incubation中 5, ...
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https://www.riss.kr/link?id=A19657340
1973
Korean
510.000
학술저널
245-254(10쪽)
0
상세조회0
다운로드국문 초록 (Abstract)
Reduced glutathione (GSH)의 組織細胞內로의 移動樣相의 一端을 알고져 마우스 大腦의 切片을 作成하고 이것을 1mM, 2mM 및 3mM의 GSH溶液中에 둔後 4C, 25C 및 37C의 溫度下에서 incubate 하고 incubation中 5, ...
Reduced glutathione (GSH)의 組織細胞內로의 移動樣相의 一端을 알고져 마우스 大腦의 切片을 作成하고 이것을 1mM, 2mM 및 3mM의 GSH溶液中에 둔後 4C, 25C 및 37C의 溫度下에서 incubate 하고 incubation中 5, 15, 30, 60 및 120分에서 各各 組織內의 GSH 및 GSSG(oxidized glutathione)을 定量하고 이 兩者의 合計로서 總 SH基(sulfhydryl)의 量으로 하여 正常群 및 對照群의 그것과 比較한 結果 다음과 같은 結果를 얻었다.
1) 正常 마우스 大腦組織의 GSH, GSSG 및 總 SH基의 量은 各各 2.33±0.26, 1.72±0.27, 및 4.05±0.27μmol/gm wet. wt.이었다.
2) 大腦組織이 GSH 및 GSSG의 量은 incubation의 溫度가 4C 및 25C에서는 incubation溶液中의 GSH의 濃度와 無關하게 時間의 經過에 따라 큰 差異가 없었고 正常群 및 名對照群의 그것과 比較해서도 서로 비슷한 傾向을 나타내었다.
3) 37℃에서 incubate 하였을 때의 大腦組織의 GSH, GSSG 및 總 SH基의 量은 incubationd溶液中의 GSH濃度에 比例하여 增加하였고 또한 實驗時間 120分까지 繼續 增加되는 傾向을 나타내었다.
다국어 초록 (Multilingual Abstract)
Glutathione, atripeptide abundantly distributed among the animal and plant world, is known to exert some important physiological actions in the body, il e. ; paticipation in various enzymatic reaction, membrane tarnsport and action mechanism of some p...
Glutathione, atripeptide abundantly distributed among the animal and plant world, is known to exert some important physiological actions in the body, il e. ; paticipation in various enzymatic reaction, membrane tarnsport and action mechanism of some peptide hormones. Also, the effectiveness of reduced glutathione (GSH) ofr radioprotection has recently been established.
However, reports on the transport mechanism of GSH through the cell membrance is scanty, and little is known whether GSH is transported through the cell membrane by active transport or facilitated diffusion, or otherwise.
In the present study, an effort was made to observe the transport mechanism of GSH by using the brain tissue of the mouse as the model.
Whole brain was carefully removed from the normal mouse, and the brain slice of approximately 0.2mm in thickness was prepared manually.
The slice was incubated in the solution of GSH in the concentration of 1mM, 2mM, and 3mM temperature of the incubation was set at 4C, 25C and 37C. At 5, 15, 30, 60 and 120 min of the incubation, the slice was taken out and carefully washed with Krebs-Ringer phosphate buffer (KRP).
GSH level ws measured by Ellman's method and GSSG (oxidized glutathione) was measured by the electrolytic reduction method described by Dohan and Woodward. The total SH (sulfhydryl) group was claculated by the sum of GSH and GSSG. The control was set in each temperature group, in which the experimental procedures were identical as in the experimental groups but the incubation was carried out in the absence of GSH and only in KRP.
Results thus obtained are summarized as follows.
1) Normal value of GSH, GSSG and total SH group of the mouse brain was 2.33±0.26, 1.72±0.27 and 4.05±0.27μmol/gm wet. wt., respectively.
2) When the incubation was carried out at 4C and 25C, GSH and GSSG levels of the mouse brain were similar in all the groups including the normal and control regardless of the concentration of GSH throughout the entire experiment.
3) When the incubation temperature was set at 37C, the levels of GSH, GSG and total SH group increased in proportion to the concentration of GSH, and the increase was continuous till 120 min.
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