Effect of butanol extract of maturated mahkota dewa (Phaleria macrocarpa) fruit on kidney tissue of Mice (Mus musculus)

Mahkota dewa (Phaleria macrocarpa [Scheff.] Boerl.) is an Indonesians traditional medicinal plant used to treat various diseases, such as diabetes mellitus, hemorrhoid, impotency and cancer. Almost all parts of the plants canbe used as traditional medicine, but if directly consumed, it can cause swollen, sprue, numb at tongue, fever, even unconsciousness. This research was carried out to find out recovery of liver tissue damage of mice administered intraperitoneally with subchronic dosage of butanol extract 170 mg/kg body weight. Observation on first week showed that there is light degeneration (vacuolization) which is getting better on second week and apparentlynormal on forth week.

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Microscopic Description of Mus Musculus Kidney Preparation Deparafinized with Olive Oil in Eosin (HE) Hematoxylin (HE) Staining

Jaringan Laboratorium Medis ◽

10.31983/jlm.v3i1.8005 ◽

2021 ◽

Vol 3 (1) ◽

pp. 61-66

Author(s):

Ela Nur Pratiwi ◽

Desy Armalina

Keyword(s):

Olive Oil ◽

Mus Musculus ◽

Visual Fields ◽

Kidney Tissue ◽

Carcinogenic Effect ◽

Microscopic Appearance ◽

Skin Erythema ◽

Acute Neurotoxicity ◽

Descriptive Approach ◽

Hematoxylin Eosin

Deparaffinization is a stage before the staining process to remove/dissolve paraffin so that the absorption of color in tissue preparations is maximized. Deparaffinization is usually carried out using xylol and toluol. Xylol has toxic effects including acute neurotoxicity, heart and kidney damage, hepatotoxicity, fatal blood dyscrasias, skin erythema, dry skin, peeling skin, and also has a carcinogenic effect. The toxicity effect of olive oil is lower than that of xylol. Oils that have non-polar properties can remove the remaining paraffin contained in the tissue. The purpose of this study was to determine the microscopic appearance of the kidney tissue preparations of mice deparaffinized with olive oil on hematoxylin eosin (HE) staining. The type of research used is experimental research which is analyzed with a descriptive approach. The results of the assessment of preparations deparaffinized with xylol in 80 visual fields obtained 100% good preparations and preparations deparaffinized with olive oil in 80 visual fields obtained 0% poor preparations, 11.3% poor preparations, and 88.7% good preparation. So it can be said that better results are found in the microscopic picture of the kidney preparations of mice (Mus musculus) deparaffinized with xylol.

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UJI EFEK ANALGESIK EKSTRAK DAUN MAHKOTA DEWA (Phaleria macrocarpa) PADA MENCIT (Mus musculus)

Jurnal e-Biomedik ◽

10.35790/ebm.1.2.2013.3249 ◽

2014 ◽

Vol 1 (2) ◽

Author(s):

Dinar Salsabila Tone ◽

Christi Mambo

Keyword(s):

Treatment Group ◽

Medicinal Plant ◽

Mus Musculus ◽

Analgesic Effect ◽

Positive Control ◽

Negative Control ◽

Control Group ◽

Male And Female ◽

Average Value ◽

Phaleria Macrocarpa

ABSTRACTThe plant of Mahkota Dewa is a traditional plant which is used as a medicinal plant whose benefits are located in almost parts where it contains flavonoid and saponin compounds that have a variety of effects and one of them is analgesic effect. This research aims to determine the analgesic effect of the extract of Mahkota Dewa leaf (Phaleria macrocarpa) in mices (Mus musculus). This research uses an experimental method using nine male and female mices which are divided into three groups: the positive control group that was given aspirin and the negative control that was given aquades and the treatment group that was given the extract of the Mahkota Dewa leaf. The research is done by giving the stimulus of pain in the form of heat 55o.C and then observes the response of the tested animal such as jumping or licking its legs and at the minute of 0 before treatment, and at the minutes of 30, 60, 90, 120 after the treatment. The average value of the number of respons of mices which were given the extract of the Mahkota Dewa leaf decreases from the 30th minute until the 90th minute. Conclusion. The extract of Mahkota Dewa leaf has an analgesic effect in Mouse.Key Word: Analgesic, Aspirin, Mahkota Dewa leaf (Phaleria macrocarpa)ABSTRAKTanaman mahkota dewa merupakan tumbuhan tradisional yang digunakan sebagai tumbuhan obat yang manfaatnya terletak hampir di seluruh bagian dimana di dalamnya terkandung senyawa-senyawa flavonoid dan saponin yang mempunyai bermacam-macam efek dan salah satunya adalah efek analgesik. Penelitian ini bertujuan untuk mengetahui efek analgesik dari ekstrak daun mahkota dewa (Phaleria macrocarpa) pada mencit (Mus musculus). Penelitian ini menggunakan metode eksperimental dengan menggunakan 9 ekor mencit jantan dan betina yang dibagi atas 3 kelompok yaitu kelompok kontrol positif yang diberi obat aspirin, kontrol negatif yang diberi aquades dan kelompok perlakuan yang diberi ekstrak daun mahkota dewa. Penelitian dilakukan dengan cara memberi rangsangan nyeri berupa suhu panas 55o.C kemudian mengamati respon hewan uji berupa melompat dan atau menjilat kaki pada menit ke-0 sebelum perlakuan, dan pada menit ke-30, 60, 90, 120 setelah perlakuan. Nilai rata-rata jumlah respon mencit yang diberikan ekstrak daun mahkota dewa mengalami penurunan dari menit ke-30 sampai menit ke-90. Kesimpulan. Ekstrak daun mahkota dewa memiliki efek analgesik pada mencit.Kata kunci: Analgesik, Aspirin, Daun Mahkota Dewa (Phaleria macrocarpa)

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Efek Antihiperurisemia Ekstrak Etanol Daun Mahkota Dewa (Phaleria macrocarpa) Scheff. Boerl.) pada Mencit Putih (Mus musculus)

Proceeding of Mulawarman Pharmaceuticals Conferences ◽

10.25026/mpc.v3i2.93 ◽

2016 ◽

Vol 3 ◽

pp. 96-103

Author(s):

Aisyah Anasia Apriani ◽

Wisnu Cahyo Prabowo ◽

Arsyik Ibrahim

Keyword(s):

Mus Musculus ◽

Phaleria Macrocarpa

Salah satu tanaman yang digunakan masyarakat sebagai obat tradisional untuk asam urat adalah daun mahkota dewa (Phaleria macrocarpa) Scheff. Boerl.). Penelitian ini bertujuan untuk mengetahui rendeman dan metabolit sekunder daun mahkota dewa, mengetahui efek ekstrak etanol daun mahkota dewa (Phaleria macrocarpa)Scheff. Boerl.) serta mencari dosis efektifnya sebagai antihiperurisemia pada mencit betina (Mus musculus), Uji ini dilakukan dengan cara membagi 21 ekor mencit dibagi menjadi 7 kelompok. Tiap kelompok mendapat perlakuan sebagai berikut: Kelompok 1: Kontrol Negatif (Na CMC 0,5%), Kelompok II: Kontrol Positif (Allopurinol dosis 100 mg/70Kg BB), Kelompok III-VII: Ekstrak etanol dosis 25, 50, 75, 100 dan 125 mg/Kg BB. Untuk memberikan kondisi Hiperurisemia, hewan coba diinduksi Kalium Oksonat 300 mg/Kg BB secara ip dan diberikan suspensi hati ayam 1,25 g/KgBB. Rendemen ekstrak etanol diperoleh sebesar 20,3 %. Hasil penelitian menunjukkan ekstrak etanol daun mahkota dewa (Phaleria macrocarpa) memiliki efek sabagai penurun asam urat. Analisis statistik dengan uji BNJD menunjukan dosis 50 mg/Kg BB adalah dosis efektif sebagai penurun kadar asam urat.

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Profile Microscopic Profile of Mice (Mus Musculus) Kidney Tissue Fixed with 10% Honey Concentration for 24 Hours

Jaringan Laboratorium Medis ◽

10.31983/jlm.v3i2.8066 ◽

2021 ◽

Vol 3 (2) ◽

Author(s):

Tasya Vita Brilian

Keyword(s):

Mus Musculus ◽

Visual Fields ◽

Kidney Tissue ◽

Chemical Substance ◽

Original Form ◽

Microscopic Image ◽

Study Approach ◽

Long Time ◽

Qualitative Descriptive ◽

Honey Solution

Fixation is used to maintain tissue structure in its original form “life-like state” and can protect proteins and tissue components from degeneration. The solution commonly used is 10% NBF. Formaldehyde is chemical substance that is toxic and not environmentally friendly, several studies have shown alternative substitutes fixation, one of which is the honey solution. The study of Mohammed et al (2020) fixated tissue with honey 10% and 20% shown good coloring properties and similar clarity to fixated with formalin 10%. Honey has acidic and dehydrating properties allow most microorganisms to be killed so that tissues will last for a long time. The research objective is to findout the description of microscopic of mice (Mus musculus) kidney tissue which were fixation using 10% honey solution for 24 hours. The research is included in qualitative descriptive research. The research design used was a non-eksperimental with a purposive sampling study approach. The sample used was 32 preparation with total of microscopic overview is 160. Microscopic image of mice (Mus musculus) kidney tissue fixed using 10% honey solution for 24 hours in 80 visual fields were 12.5% of the preparations is not good and 87.5% is good preparations. The microscopic image of mice (Mus musculus) kidney tissue fixed using 10% NBF is better than of the microscopic image of mice (Mus musculus) kidney tissue fixed with 10% honey for 24 hours.

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Freeze-Etch Crystal-Like Structures in Membranous Glomerulosclerosis

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100063883 ◽

1969 ◽

Vol 27 ◽

pp. 394-395

Author(s):

Burton B. Silver

Keyword(s):

Electron Microscopy ◽

Light Microscopy ◽

Sodium Hypochlorite ◽

Kidney Tissue ◽

Extraction Process ◽

Donor Kidney ◽

Unknown Substance ◽

Etched Surface ◽

Standard Fixation ◽

Diseased Kidney

Tissue from a non-functional kidney affected with chronic membranous glomerulosclerosis was removed at time of trnasplantation. Recipient kidney tissue and donor kidney tissue were simultaneously fixed for electron microscopy. Primary fixation was in phosphate buffered gluteraldehyde followed by infiltration in 20 and then 40% glycerol. The tissues were frozen in liquid Freon and finally in liquid nitrogen. Fracturing and replication of the etched surface was carried out in a Denton freeze-etch device. The etched surface was coated with platinum followed by carbon. These replicas were cleaned in a 50% solution of sodium hypochlorite and mounted on 400 mesh copper grids. They were examined in an Siemens Elmiskop IA. The pictures suggested that the diseased kidney had heavy deposits of an unknown substance which might account for its inoperative state at the time of surgery. Such deposits were not as apparent in light microscopy or in the standard fixation methods used for EM. This might have been due to some extraction process which removed such granular material in the dehydration steps.

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A Comparison Between Sterological Point Counting and Digitizing Tablets

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100120023 ◽

1985 ◽

Vol 43 ◽

pp. 666-667

Author(s):

John M. Basgen ◽

Eileen N. Ellis ◽

S. Michael Mauer ◽

Michael W. Steffes

Keyword(s):

Electron Microscopy ◽

Kidney Tissue ◽

Volume Density ◽

Diabetic Patients ◽

Normal Kidney ◽

Point Counting ◽

Normal Kidney Tissue ◽

Biopsy Specimens ◽

Mitochondrial Volume ◽

Kidney Lesions

To determine the efficiency of methods of quantitation of the volume density of components within kidney biopsies, techniques involving a semi-automatic digitizing tablet and stereological point counting were compared.Volume density (Vv) is a parameter reflecting the volume of a component to the volume that contains the component, e.g., the fraction of cell volume that is made up of mitochondrial volume. The units of Vv are μm3 /μm3.Kidney biopsies from 15 patients were used. Five were donor biopsies performed at the time of kidney transplantation (patients 1-5, TABLE 1) and were considered normal kidney tissue. The remaining biopsies were obtained from diabetic patients with a spectrum of diabetic kidney lesions. The biopsy specimens were fixed and embedded according to routine electron microscogy protocols. Three glomeruli from each patient were selected randomly for electron microscopy. An average of 12 unbiased and systematic micrographs were obtained from each glomerulus and printed at a final magnification of x18,000.

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Electron microscopic study of the membrane glycoproteins in the rat kidney after cisplatin treatment

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100156547 ◽

1989 ◽

Vol 47 ◽

pp. 912-913

Author(s):

S.K. Aggarwal

Keyword(s):

Alkaline Phosphatase ◽

Rat Kidney ◽

Light And Electron Microscopy ◽

Kidney Tissue ◽

Membrane Glycoproteins ◽

Electron Microscopic ◽

Before And After ◽

Interstrand Cross Links ◽

Cross Links

The proposed primary mechanism of action of the anticancer drug cisplatin (Cis-DDP) is through its interaction with DNA, mostly through DNA intrastrand cross-links or DNA interstrand cross-links. DNA repair mechanisms can circumvent this arrest thus permitting replication and transcription to proceed. Various membrane transport enzymes have also been demonstrated to be effected by cisplatin. Glycoprotein alkaline phosphatase was looked at in the proximal tubule cells before and after cisplatin both in vivo and in vitro for its inactivation or its removal from the membrane using light and electron microscopy.Outbred male Swiss Webster (Crl: (WI) BR) rats weighing 150-250g were given ip injections of cisplatin (7mg/kg). Animals were killed on day 3 and day 5. Thick slices (20-50.um) of kidney tissue from treated and untreated animals were fixed in 1% buffered glutaraldehyde and 1% formaldehyde (0.05 M cacodylate buffer, pH 7.3) for 30 min at 4°C. Alkaline phosphatase activity and carbohydrates were demonstrated according to methods described earlier.

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Localization of cell-surface and basement-membrane heparan-sulfate proteoglycans using the malaria circumsporozoite protein

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100169201 ◽

1994 ◽

Vol 52 ◽

pp. 294-295

Author(s):

U. Frevert ◽

S. Sinnis ◽

C. Cerami ◽

V. Nussenzweig

Keyword(s):

Heparan Sulfate ◽

Protein A ◽

Kidney Tissue ◽

Plasmodium Species ◽

Its Region ◽

Basement Membranes ◽

Heparan Sulfate Proteoglycans ◽

Infected Mosquito ◽

Complement Components ◽

Region Ii

Malaria sporozoites, which invade hepatocytes within minutes after transmission by an infected mosquito, are covered with the circumsporozoite (CS) protein, which in all Plasmodium species contains the conserved region II-plus. This region is also found as a cell-adhesive motif in a variety of host proteins like thrombospondin, properdin and the terminal complement components.The CS protein with its region II-plus specifically binds to heparan sulfate proteoglycans (HSPG) on the basolateral surface of hepatocytes in the space of Disse (FIG. 1), to certain basolateral cell membranes and basement membranes of the kidney (FIG. 2) as well as to heparin in the granules of connective tissue mast cells. The distribution of the HSPG receptors for the CS protein was examined by incubation of Lowicryl K4M or LR White sections of liver and kidney tissue with the recombinant CS ligand, whose binding sites were detected with a monoclonal anti-CS antibody and protein A gold.

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