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AKTIVITAS ANTIDIABETES KOMBINASI EKSTRAK TERPURIFIKASI HERBA SAMBILOTO (Andrographis paniculata (Burn.F.) NESS.) DAN METFORMIN PADA TIKUS DM TIPE 2 RESISTEN INSULIN Eka Siswanto Syamsul; Agung Endro Nugroho; Suwijiyo Pramono
Majalah Obat Tradisional Vol 16, No 3 (2011)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (682.952 KB) | DOI: 10.22146/tradmedj.8049

Abstract

A. paniculata is a plant that can be used to overcome the disease diabetes. In DM there is a possibility of the use of therapy with oral hypoglycemic drugs, for example: metformin. This research was conducted using a complete random method indirectional pattern. This study aims to determine the potential of the combination of purified extract of sambiloto herbs and enhancement effects of metformin on blood glucose levels decrease in insulin resistant rats. Test animals used were divided 4 groups, group 1: metformin 45 mg / kg (positive control), group 2: purified extract of sambiloto herbs 434.6 mg/ kg, group 3: a combination of metformin 45 mg / kg BW with the extract of 434.6 mg/ kg (combination 1), and group 4: metformin 22.5 mg/ kg body weight with extract 434.6 mg/ kg (combination 2). Test animals are insulin resistant type 2 DM was made by administering 1.8 g fructose / kg body weight and fat diet for 50 days. Assay of glucose using a reagent kit. Observation of GLUT-4 expression in muscle cells by using immunohistochemical techniques. Insulin resistance rats was tested by using three parameters: (1) testing of blood glucose levels preprandial and postprandial (2) the hypoglycaemic activity of glibenclamide, and (3) observations of GLUT-4 protein expression in muscle tissue. Test results show that the animals had insulin resistant. Results, in this research antidiabetic activity assay indicate that the hypoglycaemic for combination 1 and combination 2 lower compared to a single administration of metformin or purified extract (p<0,05). From the above results concluded that the combination of sambiloto extract purified with metformin does not increase the potency of antidiabetic in single use.
AKTIVITAS ANTIINFLAMASI REBUSAN KULIT BATANG JAMBU METE (Anacardium occidentale L.) PADA UDEMA KAKI TIKUS TERINDUKSI KARAGENIN Lini Veriony; Sudarsono Sudarsono; Agung Endro Nugroho
Majalah Obat Tradisional Vol 16, No 3 (2011)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (736.16 KB) | DOI: 10.22146/tradmedj.8052

Abstract

Hot water extract of cashew nut’s stem bark (Anacardium occcidentale L.) traditionally has been used as mouth washer to heal mouth and gum inflammation. Combination of aqueous extract of cashew nut stem bark and grape juice have anti-inflammatory activity. Cashew nut stem bark contains gallic acid and anacardic acid that had anti-inflammatory effect. The aim of this research is to observe anti-inflammatory activity of the hot water extract of Cashew nut’s stem bark compared to Indomethacin Non-Steroid Anti-inflammatory Drug. This research’s process consists of collection of the stem barks, extraction of the stem bark by hot water, qualitative analysis of gallic acid and anacardic acid, measurement total phenolic value, free radical scavenging and antiinflamatory activity assay. The hot water extract of stem bark was used to observe anti-inflammatory activity by 1.25; 2.5; 5g/kgBB and as positive control was indomethacin 10 mg/kgBB. The result of edema volume determination were counted as area under curve value and anti-inflammatory percentage and then the data were analyzed to evaluate the data difference of every group. The anti-inflammatory activity of 1.25; 2.5 and 5g/kgBB were not significantly different compared to 10 mg/kg BB indomethacin. The total phenolic concentration was gradually decreasing with the increasing concentration of the hot water extract of stem bark. The free radical scavenging DPPH activity at 1mg/mL hot water extract of stem bark was poorly than gallic acid 1mg/mL.
EFEK SENYAWA FLAVONOIDS DARI KEMUNING (Murraya paniculata [L.] Jack.) TERHADAP PELEPASAN HISTAMIN DARI KULTUR SEL MAST Agung Endro Nugroho; Sugeng Riyanto; Mohamad Aspollah Sukari; Kazutaka Maeyama
Majalah Obat Tradisional Vol 15, No 1 (2010)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (503.985 KB) | DOI: 10.22146/tradmedj.8066

Abstract

Murraya paniculata [L.] Jack. (Kemuning) is a plant that grows widely in some areas of Indonesia. Studies related to this plant have been widely explored especially isolation of its active compounds. The plant contents several active compounds such as flanovoids. In the study, three flavonoid isolated from M. paniculata were evaluated for their effect on histamine release from mast cells (RBL-2H3 cells). These compounds were 3,3’,4’,5,5’,6,7,8-octamethoxyflavone; 3,3’,4’,5,5’,6,7-heptamethoxyflavone and 3, 3’, 4’, 5, 5’, 7–hexamethoxyflavone. The histamine inducers used in the study were DNP24-BSA dan thapsigargin, inducing the histamine release immunologically and non-immunologically, respectively. In the study, heptamethoxyflavone and hexamethoxyflavone did not influence the histamine release from mast cells significantly. However, octamethoxyflavone could increase the histamine release from RBL-2H3 cells in absence and presence the histamine inducers. The flavanoid could increase the release of histamine up to 50 %. Based on the results, polymethoxy moieties at the structure of flavonoid have a significant role to emerge the histamine-release stimulating effect from mast cells. 
EVALUASI EFEK ANTI-DIABETES MELITUS EKSTRAK TERPURIFIKASI Andrographis paniculata (Burm. f.) Nees DAN ANDROGRAFOLID DENGAN PARAMETER INDEKS HOMA-IR Ignatius Ryan Adriawan; Mohamad Andrie; Rina Susilowati; Suwidjiyo Pramono; Agung Endro Nugroho
Majalah Obat Tradisional Vol 19, No 1 (2014)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (748.432 KB) | DOI: 10.22146/tradmedj.8086

Abstract

Diabetes mellitus type 2 was induced by high fat diet and fructose. The insulin resistance and hyperinsulinemia compensatory can be measured by index homeostatic model assessment – insulin resistance (HOMA-IR). Andrographis paniculata (Burm. f.) Nees is a traditional plant can be used to treat diabetes mellitus and the main active compound of this plant is Andrographolide. The objective of this study is to evaluate the effect of purified extract of Andrographis paniculata (Burm. f.) Nees and andrographolide on HOMA-IR index of High fat diet and fructose induced Wistar Rats. This study is quasi-experimental and data analysis was using Kruskal-Wallis test. The result showed that purified extract of Andrographis paniculata and andrographolide decreased HOMA-IR index. Purified extract of Andrographis paniculata 1303,8 mg/kg decreased HOMA-IR index by 82,05 %.
EFEK PENGHAMBATAN EKSTRAK N-HEKSANA BUAH MENGKUDU (Morinda citrifolia L.) TERHADAP REAKSI ANAFILAKSIS KUTANEUS AKTIF PADA TIKUS WISTAR YANG DIINDUKSI VAKSIN HEPATITIS B Ediati Sasmito; Agung Endro Nugroho; Yose V. Sagala
Majalah Obat Tradisional Vol 19, No 1 (2014)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (896.869 KB) | DOI: 10.22146/tradmedj.8089

Abstract

Noni (Morinda citrifolia L.) is one of medicinal plants that are  commonly known for its medical treatment usage. Noni is reported for the pharmacological effects, including analgesic, antihypertensive and immunomodulator. This research aims to prove that the n-hexane extract of noni fruits can inhibit active cutaneous anaphylaxis reaction in male wistar rats induced hepatitis B vaccine. This research used an active cutaneous anaphylaxis methode followed by hystopathological observation. Active cutaneous anaphylaxis test was done for 2 weeks. Test animals were divided into five groups: untreated control, treatment with n-hexane extract of noni dose of 50mg, 100mg dan 200mg/kgBW rats, and cromolyn treated group with dose of 2. mg/kg BW rats as positive control.  Animals were sensitized 2times (once every week) with hepatitis B vaccine (dose of 145µg/kgBW) subcutaneously on the back. In the second week, random four rats of each groups were sacrificed and the skin tissues and livers were taken. Tissues were created as histopathology preparations with hematoxyllin-eosin coloring. The presence of anaphylaxis reactions, shown by inflammatory cell infiltration, were observed from the histopathology preparations. The result of this research showed that the administration of n-hexane extract of noni fruits treatment dose of 50mg, 100mg, and 200mg/kgBW on male Wistar rats induced hepatitis B vaccine can inhibit active cutaneous anaphylaxis reaction.
PENGARUH KOMBINASI EKSTRAK TERPURIFIKASI HERBA SAMBILOTO (Andrographis paniculata (Burm.f.) Nees) DAN HERBA PEGAGAN (Centella asiatica (L.) Urban) TERHADAP TRANSLOKASI PROTEIN GLUT-4 PADA TIKUS DIABETES MELLITUS TIPE 2 RESISTEN INSULIN Novena Yety Lindawati; Agung Endro Nugroho; Suwijiyo Pramono
Majalah Obat Tradisional Vol 19, No 2 (2014)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (929.168 KB) | DOI: 10.22146/tradmedj.8142

Abstract

Sambiloto herb (Andrographis paniculata (Burm. f.) Nees.) and pegagan herb (Centella asiatica (L.) Urban) are excellent medicinal plants which are being developed as traditional for antidiabetic. The research aims to see the effect of combination from purified extract of sambiloto herb and pegagan herb of translocation of GLUT-4 protein in model type 2 diabetes mellitus rats-insulin resistance compared with the use of each purified extract. Test preparations were divided into 8 groups include three from combination purified extract of sambiloto herb and pegagan herb: I (912,1: 300), II (651,5: 500), III (390,9: 700) in mg/kg BW, IV (purified extract of sambiloto herb 1303 mg/kg BW), V (purified extract of pegagan herb 1000 mg/kg BW), VI (positive control metformin 45 mg/kg BW), VII (negative control CMC-Na 0.5%) and VIII (normal control). Parameters measured semi quantitative data translocation of GLUT-4 protein in cells muscles of the thigh (soleus muscle) rats using Immunohistochemistry methods. Test animals are of type 2 diabetes mellitus insulin-resistance was induced by fructose (1,8 g/kg BW) and fat-rich food (95% pellet, 5% egg yolks and 5 mL/ 200 g BW lard) for 70 days. Determination of insulin resistance used 3 parameters such as blood glucose levels, lipid levels (triglycerides, LDL, cholesterol, and HDL), and hypoglikemic tests with glibenklamid compared to normal controls animals. Insulin resistance test results using statistical analysis Independent Samples t-Test showed significant differences (p< 0.05) between normal rats with fat-fructose rats at day-50 and -70. This indicate fat-fructose rats indicated type 2 DM insulin resistance. Group of combination I (combination purified extract of sambiloto herb and pegagan herb (912,1: 300 mg/kg BB) showed effect of translocation of GLUT-4 protein was better than each purified extract with significantly p<0.05 with oneway ANOVA.
PENENTUAN AKTIVITAS ISOLAT ANDROGRAFOLID TERHADAP α-AMILASE DAN α-GLUKOSIDASE MENGGUNAKAN METODE APOSTOLIDIS DAN MAYUR Ichwan Ridwan Rais; Agung Giri Samudra; Sitarina Widyarini; Agung Endro Nugroho
Majalah Obat Tradisional Vol 18, No 3 (2013)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (202.049 KB) | DOI: 10.22146/tradmedj.8219

Abstract

Disorders of carbohydrate metabolism can lead to diabetes mellitus. Carbohydrates  are metabolized in the gastrointestinal tract  into simple glucose and absorbed into the bloodstream and affected blood glucose levels. The absorption process is catalyzed by α- 1 ,4 - glycoside breaking bond  enzyme , namely α - amylase and α -1 ,6 - glycoside breaking bond  enzyme, namely α – glucosidase. They are found in the intestinal cells. Research had been conducted in an effort to develop an alternative treatment of diabetes mellitus by testing the ability of isolates of andrographolide in inhibiting α-amylase activity and α-glucosidase in vitro. Andrographolide isolates showed fairly good activity in inhibiting α-amylase ( IC50 = 1,.49 mg/mL) and weak in inhibiting α-glucosidase (IC50 = 38,86 mg/mL). Inhibition of α-amylase activity is evidence of one mechanism of andrographolide in reducing carbohydrate metabolism that can affect blood glucose levels and indicates that andrographolide is  a potential alternative medicine in addressing diabetes mellitus .
Marmin of Aegle Marmelos Correa Antagonizes AChM3 Receptors: In Silico and In Vitro Studies on Isolated-Guinea Pig Illeum Smooth Muscle Agung Endro Nugroho; Puguh Noviarsito; Sugeng Riyanto
Journal of Mathematical and Fundamental Sciences Vol. 46 No. 3 (2014)
Publisher : Institute for Research and Community Services (LPPM) ITB

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.5614/j.math.fund.sci.2014.46.3.6

Abstract

Marmin is a coumarin derivative compounds isolated from the bark and roots of Aegle Marmelos Correa. Previously, ethanolic extract of leaves of Aegle Marmelos Correa on isolated ileum showed antagonism effect on the contraction induced by histamine. Besides H1 receptor, there is also muscarinic acetylcholine (AChM)receptors involved in the mechanism of ileum contraction. Marmin is predicted to antagonize on AChM3 receptors.This study aimed to determine the effect of marmin on smooth muscle contraction of isolated guinea pig ileum induced by metacholine, an agonist of AChM3 receptor. The method in the study were in vitro (isolated organ) and in silico (docking PLANTS). In the in vitro study, marmin exhibited a competitive antagonists effect at the concentration of 100 μM (pA2 value of 1,728) on the AChM3 receptors. Reversibility assay on AChM3 receptors showed that by washing the ileum with Tyrode buffer every 6 minutes for 30 minutes, the bond of marmin to the receptor was still not completely detached. In the in silico study, marmin was observed to be bound to AchM3 receptors (docking score: -102.086). Marmin bond was weaker than that of native ligand of AChM3 receptor (tiotropium, docking score: -115.107), however, stronger than that of AChM3 receptor agonist and antagonist. Based on the results, we conclude that marmin have a competitive antagonist activity on AChM3 receptor.
Molecular Docking Analysis of Ginger Active Compound on Transient Receptor Potential Cation Channel Subfamily V Member 1 (TRPV1) Fifteen Aprila Fajrin; Agung Endro Nugroho; Rina Susilowati; Arief Nurrochmad
Indonesian Journal of Chemistry Vol 18, No 1 (2018)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (358.623 KB) | DOI: 10.22146/ijc.28172

Abstract

Ginger had been reported to ameliorate painful diabetic neuropathy (PDN) in an animal model. Gingerol and shogaol were active compounds of ginger that potentially act on transient receptor potential cation channel subfamily V member 1 (TRPV1), a key receptor in PDN. This study aims to predict the binding of gingerol and shogaol to TRPV1 using an in silico model. The ligands of the docking study were 3 chemical compounds of each gingerol and shogaol, i.e. 6-shogaol, 8-shogaol, 10-shogaol, 6-gingerol, 8 gingerol and 10-gingerol. Capsaicin, a TRPV1 agonist, was used as a native ligand. The TRPV1 structure was taken from Protein Data Bank (ID 3J9J). The docking analysis was performed using Autodock Vina. The result showed that among the ginger active compounds, 6-shogaol had the strongest binding energy (-7.10 kcal/mol) to TRPV1. The 6-shogaol lacked the potential hydrogen bond to Ile265 of TRPV1 protein, which capsacin had. However, it's binding energy towards TRPV1 was not significantly different compared to capsaicin. Therefore, 6-shogaol had potential to be developed as a treatment for PDN.