Supardjan A.M., Supardjan
Faculty of Pharmacy, Universitas Gadjah Mada. Yogyakarta, Indonesia.

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Effect of aspirin on pi-class of rat kidney glutathione S-transferase activity Yuniarti, Nunung; Martono, Sudibyo; A.M., Supardjan
INDONESIAN JOURNAL OF PHARMACY Vol 16 No 2, 2005
Publisher : Faculty of Pharmacy Universitas Gadjah Mada, Yogyakarta, Skip Utara, 55281, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (171.919 KB) | DOI: 10.14499/indonesianjpharm0iss0pp87-93

Abstract

The nonsteroids antiinflammatory compounds like curcumin and its analogues, indomethacine, and sulfasalazin have been reported to have an inhibitory effect on GST activity on an in vitro study. The aim of this research is to find out the effect of aspirin on pi-class of rat kidney GST activity in vitro using ethacrynic acid (EA) as a specific substrate for its GST class.Glutathione activity can be measured by conjugating GSH and EA catalyzed with GST. The product can be measured spectrophotometrically to result in a rate (Δ absorption/min). With the same method, aspirin was added as an inhibitor. Decreasing conjugation product indicated that there was an inhibitory activity of aspirin.The aspirin inhibitory activity using EA and CDNB (1-chloro-2,4-dinitrobenzene) as substrates are 9,090% (Extrapolated IC50 6665,03 μM) and 14,087% (Extrapolated IC50 4102,0 μM), respectively. These results have shown that aspirin can not inhibit pi-class of rat kidney cytosolic GST activity using EA and CDNB (1-chloro-2,4-dinitrobenzene) as substrates.Key words: aspirin, GSTP, kidney.
PENTAGAMAVUNON-1 MENGHAMBAT SIKLUS SEL T47D TERINDUKSI CASPASE INHIBITOR Z-VAD-Fmk PADA FASE G2-M Da’i, Muhammad; A.M., Supardjan; Jenie, Umar Anggara; M, Kawaichi; Meiyanto, Edy
JFIOnline | Print ISSN 1412-1107 | e-ISSN 2355-696X Vol 5, No 4 (2011)
Publisher : Indonesian Research Gateway

Show Abstract | Download Original | Original Source | Check in Google Scholar

Abstract

Previous experiment indicated Curcumin’s analogue Pentagamavunon-1 (2,5-bis(41-hidroxy-31,51-dimethyl)-benzilidine-cyclopentanone) has inhibitory activity on T47D cell proliferation through induction of apoptosis and cell cycle arrest at G2-M phase. This research was conducted to observe the relationship between the induction of apoptosis and inhibition of cell cycle in T47D cells induced by Pentagamavunon-1 (PGV-1). The T47D cells were treated with 2.5 PGV-1 mM; Z-VAD-Fmk 2.5 mM; (Z-VAD-Fmk 2.5 mM+PGV-1 2.5 mM). Kinetics of cell proliferation was observed with flowcytometer analysis, molecular expression was observed with Western blot methods. The results showed induction of PGV-1 and Z-VAD-Fmk stimulate the accumulation of cells in G2-M phase (39.28%), did not differ significantly with cells that  induced by PGV-1 only (34.19%). Molecular analysis showed that treatment with (PGV-1+Z-VAD-Fmk) could prevent apoptosis through inhibition of activation of Caspase-3, increased the expression of p21 and activated Cdc-2. Overall the study showed inhibition of cell cycle at G2M phase by PGV-1 compound is not affected by the activation of caspase-3. ABSTRAK Analog kurkumin Pentagamavunon-1  (2,5-bis(41-hidroksi-31,51-dimetil)-benzilidinsiklo-pentanon) telah diteliti dapat menghambat proliferasi sel melalui mekanisme induksi apoptosis dan cell cycle arrest pada fase G2-M. Penelitian ini dilakukan untuk mengamati keterkaitan antara proses induksi apoptosis dan penghambatan siklus sel pada sel T47D yang diinduksi senyawa Pentagamavunon-1 (PGV-1). Sel T47D diberi perlakuan PGV-1 2,5 mM; Z-VAD-Fmk 2,5 mM dan (Z-VAD-Fmk 2,5 mM+PGV-1 2,5 mM). Kinetika proliferasi sel diamati dengan analisis flowcytometric, ekspresi molekuler diamati dengan metode Western blot. Hasil pengamatan menunjukkan induksi (PGV-1+Z-VAD-Fmk) memacu akumulasi sel pada fase G2-M (39,28%) tidak berbeda signifikan dengan sel yang hanya diinduksi PGV-1 (34,19%). Pengamatan molekuler menunjukkan perlakuan (PGV-1+Z-VAD-Fmk) mencegah terjadinya apoptosis melalui penghambatan aktivasi Caspase-3. Secara keseluruhan penelitian menunjukkan penghambatan siklus sel pada fase G2-M oleh senyawa PGV-1 tidak tergantung oleh aktivasi Caspase-3.
PENTAGAMAVUNON-1 MENGHAMBAT SIKLUS SEL T47D TERINDUKSI CASPASE INHIBITOR Z-VAD-Fmk PADA FASE G2-M Daâ??i, Muhammad; A.M., Supardjan; Jenie, Umar Anggara; M, Kawaichi; Meiyanto, Edy
Jurnal Farmasi Indonesia Vol 5, No 4 (2011)
Publisher : Jurnal Farmasi Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.35617/jfi.v5i4.54

Abstract

Previous experiment indicated Curcuminâ??s analogue Pentagamavunon-1 (2,5-bis(41-hidroxy-31,51-dimethyl)-benzilidine-cyclopentanone) has inhibitory activity on T47D cell proliferation through induction of apoptosis and cell cycle arrest at G2-M phase. This research was conducted to observe the relationship between the induction of apoptosis and inhibition of cell cycle in T47D cells induced by Pentagamavunon-1 (PGV-1). The T47D cells were treated with 2.5 PGV-1 mM; Z-VAD-Fmk 2.5 mM; (Z-VAD-Fmk 2.5 mM+PGV-1 2.5 mM). Kinetics of cell proliferation was observed with flowcytometer analysis, molecular expression was observed with Western blot methods. The results showed induction of PGV-1 and Z-VAD-Fmk stimulate the accumulation of cells in G2-M phase (39.28%), did not differ significantly with cells that  induced by PGV-1 only (34.19%). Molecular analysis showed that treatment with (PGV-1+Z-VAD-Fmk) could prevent apoptosis through inhibition of activation of Caspase-3, increased the expression of p21 and activated Cdc-2. Overall the study showed inhibition of cell cycle at G2M phase by PGV-1 compound is not affected by the activation of caspase-3. ABSTRAK Analog kurkumin Pentagamavunon-1  (2,5-bis(41-hidroksi-31,51-dimetil)-benzilidinsiklo-pentanon) telah diteliti dapat menghambat proliferasi sel melalui mekanisme induksi apoptosis dan cell cycle arrest pada fase G2-M. Penelitian ini dilakukan untuk mengamati keterkaitan antara proses induksi apoptosis dan penghambatan siklus sel pada sel T47D yang diinduksi senyawa Pentagamavunon-1 (PGV-1). Sel T47D diberi perlakuan PGV-1 2,5 mM; Z-VAD-Fmk 2,5 mM dan (Z-VAD-Fmk 2,5 mM+PGV-1 2,5 mM). Kinetika proliferasi sel diamati dengan analisis flowcytometric, ekspresi molekuler diamati dengan metode Western blot. Hasil pengamatan menunjukkan induksi (PGV-1+Z-VAD-Fmk) memacu akumulasi sel pada fase G2-M (39,28%) tidak berbeda signifikan dengan sel yang hanya diinduksi PGV-1 (34,19%). Pengamatan molekuler menunjukkan perlakuan (PGV-1+Z-VAD-Fmk) mencegah terjadinya apoptosis melalui penghambatan aktivasi Caspase-3. Secara keseluruhan penelitian menunjukkan penghambatan siklus sel pada fase G2-M oleh senyawa PGV-1 tidak tergantung oleh aktivasi Caspase-3.