Hepatoprotective Activity of Ethyl Acetate Fraction of Senggugu’s Root Bark (Clerodendrum serratum L.Moon) on Rats Induced by CCl4

Nasrudin Nasrudin, Wahyono Wahyono, Mustofa Mustofa, Ratna Asmah

Abstract


Senggugu is a plant that has long been used to treat syphilis, typhoid, cancer, jaundice, and hypertension. The pharmacological activity of senggugu in Indonesia that have been reported include antifertility activity in leaves, mucolytic activity, anti-inflammatory and tracheospasmolytic, also antioxidant in its root bark. This study aims to determine the hepatoprotective effect of ethyl acetate extract fraction of senggugu’s root bark in rats induced by CCl4. The powder of senggugu’s root bark was extracted by terraced maceration method starts from n-hexane, ethyl acetate, to methanol, thus obtained ethyl acetate extract fraction of senggugu’s root bark (FEAKAS). The ethyl acetate extract fractions were then tested for hepatoproctective activity using doses of 25, 50, and 100 mg/Kg.BW on rats induced by CCl4. FEAKAS hepatoprotective activity was determined from the analysis of blood biochemical and oxidative stress parameters. The blood biochemical parameters included SGOT (serum glutamic oxaloacetic transaminase), SGPT (serum glutamic pyruvic transaminase), ALP (alkaline phosphatase), bilirubin, and total protein were measured with test kit. The oxidative stress parameters were measured from homogenates of liver tissue that were prepared by adding 500 mL of 50 nM Tris buffer (pH 7.4) containing 1 mM EDTA and 10 µg/mL leupeptin. The homogenates were centrifuged to obtain supernatants for measurement of oxidative stress parameters using spectrophotometer method, including MDA (malondialdehyde), GPx (glutathione peroxidase) and CAT (catalase). The results showed that the effect of FEAKAS against CCl4 induction for preventing lipid peroxidation, from both blood chemical and oxidative stress parameters, are shown at a dose of 100 mg/Kg.BW that significantly different compared to CCl4 control (ρ <0.05) on all blood chemical and oxidative stress parameters.


Keywords


Clerodendrum serratum; antioxidant; hepatoprotective effect; carbon tetrachloride

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References


Aebi, H., 1984. [13] Catalase in vitro, dalam: Enzymology, B.-M. in (Ed.), Oxygen Radicals in Biological Systems. Academic Press, hal. 121–126.

Ai, G., Liu, Q., Hua, W., Huang, Z., dan Wang, D., 2013. Hepatoprotective evaluation of the total flavonoids extracted from flowers of Abelmoschus manihot (L.) Medic: In vitro and in vivo studies. Journal of Ethnopharmacology, 146: 794–802.

Arthur, J.R., 2001. The glutathione peroxidases. Cellular and Molecular Life Sciences CMLS, 57: 1825–1835.

Ashok, S.K., Somayaji, S.N., dan Bairy, K.L., 2001. Hepatoprotective effects of GinKgo biloba against carbon tetrachloride induced hepatic injury in rats. Indian Journal of Pharmacology, 33: 260.

Bandaranayake, W.M., 2002. Bioactivities, bioactive compounds and chemical constituents of mangrove plants. Wetlands Ecology and Management, 10: 421–452.

Basu, S., 2003. Carbon tetrachloride-induced lipid peroxidation: eicosanoid formation and their regulation by antioxidant nutrients. Toxicology, Environmental and Nutritional Interactions Antioxidant Nutrients and Environmental Health, Part C 189: 113–127.

Brigelius-Flohé, R. dan Flohé, L., 2003. Is there a role of glutathione peroxidases in signaling and differentiation? BioFactors, 17: 93–102.

Del Rio, D., Stewart, A.J., dan Pellegrini, N., 2005. A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stress. Nutrition, Metabolism and Cardiovascular Diseases, 15: 316–328.

Fraschini, F., Demartini, G. dan Esposti, D., 2002. Pharmacology of silymarin . Clinical Drag Investigation, 22: 51 - 65.

Gomes, A., Alam, M.A., Datta, P., Bhattacharya, S., dan Gomes, A., 2011. Hepatoprotective activity of the edible snail (Bellamia bengalensis) flesh extract in carbon tetrachloride induced hepatotoxicity in rats. Journal of Ethnopharmacology, 138: 228–232.

Heyne, K. 1950, Tumbuhan Berguna Indonesia (diterjemahkan oleh Badan Litbang Kehutanan), Jilid III Ed 1, 1686.

Jayakumar, T., Ramesh, E., dan Geraldine, P., 2006. Antioxidant activity of the oyster mushroom, Pleurotus ostreatus, on CCl4-induced liver injury in rats. Food and Chemical Toxicology, 44: 1989–1996.

Julaeha, E., Malini, D.M., dan Sondang, O.S., 2013. 'Pengaruh pemberian senyawa C30 sterol yang diisolasi dari daun Clerodendrum serratum terhadap kualitas sperma musculus secara in vivo'. URL: https://scholar.google.co.id/scholaro&btnG=&hl=id&as_

sdt=0%2C (diakses tanggal 17/8/2016).

Narayanan, N., Thirugnanasambantham, P., Viswanathan, S., Vijayasekaran, V., dan Sukumar, E., 1999. Antinociceptive, anti-inflammatory and antipyretic effects of ethanol extract of Clerodendron serratum roots in experimental animals. Journal of Ethnopharmacology, 65: 237–241.

Nasrudin, N., 2015. Uji aktivitas antioksidan ekstrak etil asetat kulit akar senggugu (Clerodendrum serratum) asal Imogiri, Yogyakarta. e-Publikasi Ilmiah Fakultas Farmasi Unwahas Semarang, 0: 112–117.

Pareek, A., Godavarthi, A., Issarani, R., dan Nagori, B.P., 2013. Antioxidant and hepatoprotective activity of Fagonia schweinfurthii (Hadidi) Hadidi extract in carbon tetrachloride induced hepatotoxicity in HepG2 cell line and rats. Journal of Ethnopharmacology, 150: 973–981.

Prasad, M. P., Sushant, S., dan Chikkaswamy, B.K., 2012. 'Phytochemical analysis, antioksidant potential, antibakterialactivity ang molecular characterization of Clerodendrum species'. URL: https://www.researchgate.net/profile/Sushant_Shekhar/publication/260293845_

Phytochemical_analysis_antioxidant_potential_antibacterial_activity_and_molecular_characterization_of_Clerodendrum_species/links/00b7d530a741141b0b000000.pdf (diakses tanggal 17/8/2016).

Recknagel, R.O., Glende, E.A., Dolak, J.A., dan Waller, R.L., 1989. Mechanisms of carbon tetrachloride toxicity. Pharmacology & Therapeutics, 43: 139–154.

Ryder, S.D., Clinical assessment of liver disease. Medicine 2006;35(suppl. 1): 1 - 4.

Sacher, R. A., & McPherson, R. A., 2004. Tinjauan Klinis Hasil Pemeriksaan, Laboratorium. Edisi 11, diterjemahkan oleh Pandit, Wulandari, EGC, Jakarta.

Shenoy, K.A., Somayaji, S.N. dan Bairy, K.L, 2001. Hepatoprotective effects of GinKgo biloba against carbon tetrachloride induced hepatic injury in rats. Indian Journal Pharmacology, 33: 260-266.

Shrivastava, N. dan Patel, T., 2007. 'Clerodendrum and Heathcare: An Overciew'. URL: file:///C:/Users/Nasrudin/Downloads/Documents/MAPSB_1(1)142-150o.pdf (diakses tanggal 17/8/2016).

Singh, N., Kamath, V., Narasimhamurthy, K., dan Rajini, P.S., 2008. Protective effect of potato peel extract against carbon tetrachloride-induced liver injury in rats. Environmental Toxicology and Pharmacology, 26: 241–246.

Vidya, S.M., Krishna, V., Manjunatha, B.K., Mankani, K.L., Ahmed, M., dan Singh, S.D.J., 2007. Evaluation of hepatoprotective activity of Clerodendrum serratum L. IJEB Vol.45(06) [June 2007], .

Zhou, G., Chen, Y., Liu, S., Yao, X., dan Wang, Y., 2013. In vitro and in vivo hepatoprotective and antioxidant activity of ethanolic extract from Meconopsis integrifolia (Maxim.) Franch. Journal of Ethnopharmacology, 148: 664–670.

Wahyono, 1998, Isolasi Senyawa Aktif dari Kulit Akar dan Kulit Batang Clerodendron serratum Spreng. yang Berkhasiat sebagai Mukolitik, Laporan Penelitian, Majalah Farmasi Indonesia, Lembaga Penelitian UGM, Yogyakarta.

Wahyono, 2001, Isolasi Senyawa Aktif dari Kulit Akar Clerodendron serratum Spreng. yang Berkhasiat sebagai Anti-inflamasi, Laporan Penelitian, Majalah Farmasi Indonesia, Lembaga Penelitian UGM,Yogyakarta.

Wahyono, 2004, Isolasi dan Karakterisasi Senyawa yang Berkhasiat Trakeospasmolitik dan Kulit Akar Senggugu (Clerodendron serratum Spreng.), Laporan Penelitian, Grant Que Proyect-Fakultas Farmasi UGM, Yogyakarta.

Walton, P.A. dan Pizzitelli, M. 2012. Effects of peroxisomal catalase inhibition on mitochondrial function. Frontiers in Physiology 3. 108.




DOI: http://dx.doi.org/10.14499/indonesianjpharm28iss1pp10

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