Acute toxicity test of standardized ethanolic extract of Senggugu (Clerodendrum serratum L. Moon) root bark

Wahyono ., Lukman Hakim, Nurlaila ., Marlin Sulistio, Rosmulyati Ilyas


The goal of this research was to assess the potency of acute toxicity, evaluate clinical symptoms, spectrum of toxic effect and mechanism that caused the death of animal test after administration of standardized ethanolic extract of senggugu (Clerodendrum serratum L.Moon) root bark to Balb/C male mice.

The research used completely randomized design. The animal test was Balb/C male mice, healthy, age 2-3 months with uniform body weight. Twenty-five mice were grouped into 5 groups, including 1 control group with administration of 0.5 % CMC Na and 4 experimental groups. The dosage for each group were 0.73; 1.21 ; 2.03; and 3.38 g/kg of body weight, respectively. Evaluation of the toxic symptoms and death of animal test was done for 24 hours. If the animal test was died before 24 hours then it underwent surgery to take the heart, liver, lung, kidney, gastric, and intestine. In the end of the evaluation, all mice were killed to take the vital organs for histopathologic examination.

The test resulted LD50 of standardized ethanolic extract from senggugu root bark using Balb/C male mice was 1.57 g/kg of body weight. It was categorized as moderately toxic. Administration of the extract caused alterations of animal behaviours including vocalization, passiveness and mucus secretion. Histopathology examination shows infiltration of lymphocyte and neutrophil in intestinal mucous after administration of the extract.

Key words: standardized ethanolic extract, Clerodendrum serratum L.Moon, LD50

Full Text:



Anonim, 2000, Pedoman Pelaksanaan Uji Klinik Obat Tradisional, 1, 5, 14-15, Departemen Kesehatan RI, Jakarta.

Atmodjo, A. P., 1990, Album Patologi Anatomi, 15, 19, 25, 58, Airlangga University Press, Surabaya.

Balazs, T., 1970, Measurement of Acute Toxicity, In Paget, G.E. (Ed), Methods in Toxicology, 50, Blackwell Scientific Publication Oxford.

Glaister, J. R., 1986, Principles of Toxicological Pathology, 62, 64, 74, 81,83,88, 95, 116-117, 122, Taylor & Francis, London.

Greaves, M. B. P., Ch. B., Path, F.R.C., 2000, Histopathology of Preclinical Toxicity Studies, 220, 372, 545, Elsevier, Amsterdam.

Heyne, K., 1950, Tumbuhan Berguna Indonesia, diterjemahkan oleh Badan Litbang Kehutanan, Jilid III, Edisi I, 1686, Departemen Kehutanan, Jakarta.

Loomis, T. A., 1978, Toksikologi Dasar, diterjemahkan oleh Donatus,I.A., Edisi III, 3, 22, 26-27, 225-226, 228, IKIP Semarang Press, Semarang.

Lu, F. C., 1991, Toksikologi Dasar Asas, Organ Sasaran dan Penilaian Risiko, diterjemahkan oleh Nugroho,E., Edisi kedua, 86, 89, 92-93, UI Press, Jakarta.

Wahyono, 1998, Isolasi Senyawa Aktif Dari Kulit Akar Dan Kulit Batang Clerodendron serratum Spreng Yang Berkhasiat Sebagai Mukolitik, Laporan Penelitian, Lembaga Penelitian UGM, Yogyakarta

Wahyono, 2001, Isolasi Senyawa Aktif Dari Kulit Akar Clerodendron serratum Spreng Yang Berkhasiat Sebagai Antiinflamasi, Laporan Penelitian, Lembaga Penelitian UGM, Yogyakarta.

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

Wahyono, Wahyuono, S., Hakim, L., 2006, Pengembangan Akar Tanaman Senggugu (Clerodendrum serratum L. Moon), Sebagai Obat Tradisional Untuk Sesak Napas, Laporan Hasil Penelitian, BPOM RI-Fakultas Farmasi UGM



  • There are currently no refbacks.


Creative Commons License
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.

Indonesian J Pharm indexed by:

analytics View My Stats