Efek kurkumin sintesis dan Pentagamavunon-0 terhadap Produksi Progesteron Kultur Sel Luteal dengan Pemberian Forskolin
https://doi.org/10.33476/jky.v15i3.1075
Keywords:
Curcuma longa, progesterone, luteal cell culture, protein kinase AAbstract
Curcumin is one of the common traditional medicines that is often used for fertility regulation. Curcumin analogue, pentagamavunon-0/PGV-0, exerted similar effect with curcumin. Synthetic curcumin and PGV-0 possesses molecular structures similar to prostaglandin. It has been reported that luteal cells are able to produce progesterone in vitro by addition of several hormones such as LH and prostaglandin F2? (PGF2?). Stimulation of luteal cell cultures with LH and/or PGF2? in the presence of synthetic curcumin and PGV-0 will interfere with the progesterone production. Nevertheless, the precise site of action of curcumin remains unknown. The present study aims to determine the effect of synthetic curcumin and PGV-0 on the progesterone production by luteal cell cultures in the presence or absence of several known stimulators or inhibitors sucs as LH, PGF2? and forskolin, respectively. The results indicated that synthetic curcumin reduced the progesterone concentration significantly (p<0,05) in the luteal cell culture treated with solvent, LH and/or PGF2?, in the presence or absence of forskolin. In the groups treated with PGV-0, and induced with LH and/or PGF2?, the concentration of progesterone did not change significantly (p>0,05). Addition of forskolin on the control group resulted in higher progesterone concentration as that of LH. The findings indicated that synthetic curcumin inhibits progesterone production by the luteal cell cultures through the cAMP/PKA/MAP-Kinase signaling cascade, but PGV-0 might have the site of action in the PLC/PKC/MAP-Kinase signaling cascade.
References
Ammon HPT, Wahl MA 1991. Pharmacology of Curcuma longa, Planta Medica 57 :1-7.
Ammon HPT, Safayhi M, Mack T, Sabieraj J 1983. Mechanism of Antiinflamatory Action of Curcumine and Boswellic Acids. J Ethnopharmacol 38 (2-3):113 -9.
Bogan RI, Niswender GD 2007. Constitutive Steroidogenic in Ovine Large Luteal Cells May Be Mediated by Tonocally Active Protein Kinase A. Biol Reprod 77: 000 – 000.
Chin EC, Harris TE, Abayasekara DRE 2004. Changes in cAMP dependent Protein Kinase (PKA) and Progesteron secretion in Luteinizing human granulose cells. J Endocrinol 183: 39-50.
Dewi DA, Abayasekara DRE, Wheeler-Jones PD 2002. Requirement for ERK1/2 Activation in the regulation of Progesteron production in Human Granulosa-Lutein Cells Is Stimulus specific, Endocrinol., 143 (3): 877-888.
Garg SK 1974. Effect of Curcuma longa (Rhizome) on Fertility in Experimental Animals. Planta Medica. 26 : 225 – 227.
Gyles SL, Burns CJ, Whitehouse BJ, Sugden D, Marsh PJ 2001. ERKs Regulate Cyclic AMP induced Steroid Synthesis through Transcription of the Steroidogenic Acute Regulatory (StAR) Gene. J Bio Chem. 276 (14): 34888-34895.
Hasmeda M, Polya GM 1995. Inhibition of Cyclic AMP- dependent Protein Kinase by Curcumin, In: Pramono S., Jenie UA, Sudibyo RS, Gunawan D Ed. Recent Developments in Pharmacochemistry, Proceeding of the International Symposium of Curcumin Pharmacochemistry (ISCP), Aditya Media, Yogyakarta: 117-125.
Huang MT, Ma W, lou JR, Lu YP, Chang R, Newmark H, Conney AH 1995. Inhibitory Effects of curcumin on Tumorogenesis in Mice. In : Pramono S, Jenie UA, Sudibyo RS, Gunawan D Ed., Recent Developments in Curcumin Pharmacochemistry, Proceeding Of The International Symposium on Curcumin Pharmacochemis try (ISCP), Aditya Media. Yogyakarta: 47 – 61.
Khan MI, Rosberg S, Lahav M, Lamprecht SA, Selstam G, Herlitz H, Ahren K 1979. Study of the mechanism of action of the inhibitory effect of PGF2? on cyclic AMP accumulation in rat korpora lutea of various ages. Biol Reprod. 21: 1175.
Meiyanto E 1999. Kurkumin sebagai obat kanker. Menelusuri Mekanisme Aksinya, Majalah Farmasi Indonesia10 (94): 224-236.
Meiyanto E 2004. Efek Anti-Proliferatif dan Anti-Metastatik Tulang Pentagamavunon-0 terhadap kanker payudara. Laporan Akhir Riset Unggulan Terpadu X Bidabf Kesehatan. Lembaga Ilmu Pengetahuan Indonesia.
Mukhopadhyay A, Basu N, Ghatak N, Gujral PK 1982. Anti- Inflammatory and irritant Activities of Curcumin analogues in rat,. Agent and Action., 12 (4) : 508 – 515.
Niswender GD, Juengel JL, Silva PJ, Rollyson MK, Mc Intush EW 2000. Mechanism Controlling the Function and Life Span of the Corpus Luteum. Physiol Rev 80 (1) : 1 – 29.
Niswender GD 2002. Molecular Control of Luteal secretion of Progesterone. Review. Reproduction. 123: 333-339.
Soejono SK, Sutriono, Wiyanto J, Marlina U, Puspitasari S 2000. Sitotoksisitas Kurkumin Molekul Nasional pada Kultur Sel Luteal tikus (Sprague Dawley), Mediagama 2 (13) : 59 – 67.
Soejono SK, Amin SM, Nurcahyo H, Hadi RS 2001. Peran kurkumin Sintesis dan analognya (Pentagamavunon-O) pada produksi progesteron oleh kultur sel luteal Tikus (Sprague Dawley). Mediagama. III (3): 42 -49.
Stocco C, Telleria C, Gibori G 2007. The Molecular Control of Corpus Luteum: Formation, Function and Regression. Endocr Rev 28 (1): 117-149.
Tai CJ, Kang SK, Choi KC, Tzeng CR, Leung PCK 2001. Role of Mitogen Activated Protein Kinase in Prostaglandin F2? Action in Human granulosa-Luteal Cells. J Clin Endocrinol Metab 86: 375-380.
Thomas JP, Dorflinger LJ, Behrman HR 1978. Mechanism of the Rapid Antigonadotropic Action of Prostaglandins in Cultured Luteal Cells, Proc Natl Acad Sci 75 (3): 1344 – 8.
Wettschureek N, Offermanns S 2005. Mammalian G Protein and Their Cell Type Specific Functions. Physiol Rev 85 : 1159- 1204.
Zulkhah N, Soejono SK, Suwono 2000. Pengaruh kurkumin sintetik terhadap Produksi progesteron oleh kultur sel luteal tikus dengan perangsangan hCG dan PGF2?. Sains Kedokteran, Berkala Penelitian Pascasarjana Ilmu –ilmu Kesehatan, Universitas Gadjah Mada, Yogyakarta.