Effect of dental adhesives on the exudative phase of the inflammatory process in subcutaneous tissue of rats

The vascular changes in the subcutaneous connective tissue of rats induced by dentin bonding systems (one step) was studied and compared to those induced by saline solution (negative control) and Furacin (positive control), during the exudative phase of the inflammatory process. Twenty mg/kg of Evan's blue were injected intravenously in the vein of the rats' penises; 0.1 ml of each substance tested was inoculated in the subcutaneous tissue. After a 3 hour period the animals were sacrificed and their skins were excised and punched out with a standard steel 2.5 cm in diameter. The specimens were immediately immersed in 8 ml of formamide and taken to a double boiler for 72 hours at 37ºC, to remove the dye. The liquid containing the overflowed dye was filtered, analyzed in the spectrophotometer (620 nm) and classified according to the criteria established by Nagem-Filho, Pereira (1976). After statistical analysis, the irritative potential of the substances was ranked as follows: Furacin (severe) > Single Bond and Bond 1 (moderate - no significant differences between the dentin bonding systems tested) > saline solution (not significant as regards the irritation degree).

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188 EFFECT OF RABBIT SEMINAL PLASMA IN OVULATING RESPONSE

Reproduction Fertility and Development ◽

10.1071/rdv25n1ab188 ◽

2013 ◽

Vol 25 (1) ◽

pp. 243 ◽

Cited By ~ 4

Author(s):

M. Masdeu ◽

R. M. García-García ◽

P. Millán ◽

L. Revuelta ◽

O. G. Sakr ◽

...

Keyword(s):

Seminal Plasma ◽

Protein Concentration ◽

Saline Solution ◽

Experimental Period ◽

Positive Control ◽

Negative Control ◽

Corpora Lutea ◽

Blood Samples ◽

Equine Chorionic Gonadotropin ◽

Artificial Vagina

The presence of an ovulation-inducing factor (OIF) in the seminal plasma (SP) of several species with spontaneous and induced ovulation, included the rabbit, has been documented. The biochemical identity of OIF in SP remains unknown, but it seems that OIF is a protein (Ratto et al. 2011 Reprod. Biol. Endocrinol. 9, 24). The aim of this study was to determine if the protein present in the rabbit SP could induce ovulation in a dose manner and provoke changes in plasma hormone concentrations [LH and progesterone (P4)]. Semen was collected from 12 male rabbits using an artificial vagina, pooled, centrifugated at 3000g for 30 min twice and analysed by Bradford method to determine protein concentration that was 7 mg protein mL–1 of SP. After storage at –80°C, the SP was lyophilized for use at different concentrations. Twenty-four females were synchronized with an i.m. injection of 25 IU of equine chorionic gonadotropin and randomly assigned to 4 groups (n = 6). Forty-eight hours later (day 0) they were given a single i.m. dose of 1) 1 mL of saline solution (SS; negative control), 2) 20 µg of gonadorelin (GnRH; positive control), 3) 1 mL of lyophilized SP diluted in SS containing 7 mg of protein (SP7), 4) 1 mL of lyophilized SP diluted in SS containing 14 mg of protein (SP14). Blood samples for LH measurement were taken every 30 min from 30 min before injection to 2 h after treatment. Blood samples for P4 measurement were taken every 2 days from Day 0 to Day 6. Hormone determinations were made by enzyme immunoassay. Ovulation rate (OR), number of corpora lutea (CL), follicles higher than 1 mm, and total number of hemorrhagic follicles were determined after euthanasia on Day 7. Statistical analysis was performed by ANOVA. The OR was significantly higher (P < 0.0001) in GnRH than in SS, SP7, and SP14 groups (OR: 100, 0, 0, and 8.3%, respectively). Total number of CL counted in does that ovulated in GnRH and SP14 groups was not different (13.7 ± 0.8 and 9 ± 0.0 CL, respectively; P < 0.0001). No statistical differences were observed between groups on the number of follicles higher than 1 mm (GnRH: 17 ± 2.4; SS: 15 ± 1.6; SP7: 11.7 ± 2.6; SP14: 14.8 ± 0.9) and anovulatory hemorrhagic follicles (GnRH: 2.3 ± 0.9; SS: 0.2 ± 0.2; PS: 1.7 ± 0.8; PS 14: 1.7 ± 1.5). Treatment was followed by a surge in plasma LH concentration beginning 30 min after treatment to 120 min in GnRH group ranging ~75 ng mL–1, whereas in the other groups it remained at basal levels (around 20 ng mL–1; P < 0.0001). Plasma P4 concentrations were significantly increased from Day 2 to 6 (4.7 ± 0.7 to 22.3 ± 3.7 ng mL–1; P < 0.0001) only in rabbits treated with GnRH. Plasma P4 concentrations did not vary throughout the experimental period in all OIF-treated rabbits. The present study failed to demonstrate the effect of 3 different dosages of OIF of the rabbit SP on induction of ovulation. More studies are necessary to elucidate if rabbit SP could induce ovulation in rabbit females. We acknowledge CM and MEC for funding.

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Antibacterial Effect of Curcumin against Clinically Isolated Porphyromonas gingivalis and Connective Tissue Reactions to Curcumin Gel in the Subcutaneous Tissue of Rats

BioMed Research International ◽

10.1155/2019/6810936 ◽

2019 ◽

Vol 2019 ◽

pp. 1-14 ◽

Cited By ~ 2

Author(s):

Aram Mohammed Sha ◽

Balkees Taha Garib

Keyword(s):

Connective Tissue ◽

Porphyromonas Gingivalis ◽

Subcutaneous Tissue ◽

Positive Control ◽

Negative Control ◽

Biochemical Tests ◽

Inflammatory Reactions ◽

Dramatic Decline ◽

Subcutaneous Tissues ◽

Tissue Reactions

The aim of this study was to find the antibacterial potential of curcumin against Porphyromonas gingivalis and connective tissue responses to curcumin gel in the subcutaneous tissue of rats. The sample consisted of subgingival plaque collected from patients with chronic periodontitis. The P. gingivalis clinically isolated strain was confirmed by anaerobic culture, morphology, biochemical tests (Vitek ANC Kit), and PCR (16S rDNA). Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined by incubation of twofold serial dilution of broth media containing curcumin (from 100 to 0.05 µg/ml) for 48 h at 37°C. Fifteen adult Wistar rats (3-4 months old) were used and randomly divided into three groups (negative control, positive control, and experimental groups). Tubes were implanted on the back skin (45 tubes). Rats were euthanized at 7, 30, and 60 days after surgical processes, and then the samples were taken and processed to achieve conventional hematoxylin and eosin-stained slides. The MIC and MBC of curcumin against clinically isolated P. gingivalis were 12 µg/ml. Curcumin gel caused moderate inflammatory reactions at 7 and 30 days, while at 60 days, it caused dramatic decline and resulted in a nonsignificant response. Besides, curcumin gel stimulated quick reepithelialization, fibroblast proliferation, and scarring through the formation of thick bundles of well-organized collagen fibers. Curcumin has an effective antibacterial action against clinically isolated P. gingivalis at low concentration (12 µg/ml), and it was regarded as the biocompatible material in the subcutaneous tissues.

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In vitro cytotoxicity of one-step dentin bonding systems

Journal of Endodontics ◽

10.1016/s0099-2399(99)80003-x ◽

1999 ◽

Vol 25 (2) ◽

pp. 89-92 ◽

Cited By ~ 28

Author(s):

Imad Abou Hashieh ◽

Anne Cosset ◽

Jean Claude Franquin ◽

Jean Camps

Keyword(s):

In Vitro Cytotoxicity ◽

Dentin Bonding ◽

One Step ◽

Bonding Systems

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POTENSI EKSTRAK ETANOL BAWANG MERAH (Allium ascolonicum L.) DAN GARAM NaCl MENURUNKAN LUAS AREA SERTA MENINGKATKAN KONTRAKSI JARINGAN LUKA BAKAR RINGAN

Jurnal Kimia ◽

10.24843/jchem.2019.v13.i01.p09 ◽

2019 ◽

Vol 13 (1) ◽

pp. 53

Author(s):

I M. Sukadana ◽

S. Rahayu ◽

Melli Melli

Keyword(s):

Treatment Group ◽

Subcutaneous Tissue ◽

Healing Process ◽

Positive Control ◽

Negative Control ◽

Control Group ◽

Skin Damage ◽

Control Group Design ◽

Onion Extract ◽

Skin Response

Burns is a skin response and subcutaneous tissue to temperature or thermal trauma that affects skin damage. The weight or severity of tissue damage from burns is influenced by several factors including deep burns, burns area, burn location, general body health, injury mechanism and age. The area of ??burns and the percentage of wound contractions is an indicator of the healing process of minor burns. This study used 25 wistar rats divided into 5 treatment groups with randomized posttest only control group design as follows; K: given vaseline treatment (negative control), Kp: given bioplacenton treatment (positive control), P1: given salt treatment at 7.5% concentration in vaseline, P2: given onion extract treatment at 40% concentration in vaseline, and P3: given a mixture of onion extract 40% and kitchen salt at a concentration of 7,5% in vaseline. The result of One-Way ANOVA and Post Hoc Test LSD using SPSS for Windows version 19 shows P2 treatment group is onion extract of 40% give the best result concentration of onion extract so it is very potential to be developed further as light burning agent compared to P1 and P3 treatment group because of its ability to decrease the area of ??340,79 mm2 on the first day to 11,75 mm2 and increased wound contraction by 81,59% at the end of treatment

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Corrosive Effect of Probiotic And Isotonic Drinks on Dental Archwires

International Journal of Current Pharmaceutical Review and Research ◽

10.25258/ijcprr.v8i03.9211 ◽

2017 ◽

Vol 8 (03) ◽

Author(s):

Fajar Kusuma Dwi Kurniawan ◽

Dini Novita Putri ◽

Tri Nastiti Husna ◽

Eko Suhartono

Keyword(s):

Lactic Acid ◽

Treatment Group ◽

Normal Saline ◽

Saline Solution ◽

Negative Control Group ◽

Positive Control ◽

Negative Control ◽

Positive Control Group ◽

Control Group

The aim of this in vitro study was to investigate the effect of probiotic and isotonic drinks on chromium (Cr) and nickel (Ni) release from dental archwires. The conventional stainless steel dental archwires were used in this study, with 0.8 cm diameter, and 5 cm long from each sample. Total samples are 54 pieces dental archwires. The samples then divided into two major groups: (1) the probiotic (T1); and (2) isotonic (T2) drinks. Each major group consist three subgroups, such as: for the T1: (1) T1,1: as a negative control group (samples were immersed in saline solution); (2) T1,2: as a positive control group (samples were 1% lactic acid); (3) T1,3: as a treatment group (samples were immersed in normal saline + probiotic drink); and for the T2: (1) T2,1: as a negative control group (samples were immersed in saline solution); (2) T2,2: as a positive control group (samples were immersed in 1% lactic acid); (3) T2,3: as a treatment group (samples were immersed in normal saline + isotonic drink). After the immersion testing, there was a significance difference in Cr and Ni release from dental archwires between the subgroup of treatments from both probiotic and isotonic drinks (Kruskal-Wallis test followed by Mann-Whitney test; P > 0.05). In conclusion, the present study demonstrated that both probiotic and isotonic drinks induced the releasing of Cr and Ni from dental archwires.

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Total etch dentin bonding systems: scanning electron microscopy of the resin-dentin hybrid layer

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100130092 ◽

1992 ◽

Vol 50 (2) ◽

pp. 1092-1093

Author(s):

Jorge Perdigao

Keyword(s):

Composite Resin ◽

Mechanical Interlocking ◽

Hybrid Layer ◽

Agent Based ◽

Dentin Bonding ◽

Acid Agent ◽

Bond Strengths ◽

Main Component ◽

Bonding Systems ◽

New Generation

In 1955, Buonocore introduced the etching of enamel with phosphoric acid. Bonding to enamel was created by mechanical interlocking of resin tags with enamel prisms. Enamel is an inert tissue whose main component is hydroxyapatite (98% by weight). Conversely, dentin is a wet living tissue crossed by tubules containing cellular extensions of the dental pulp. Dentin consists of 18% of organic material, primarily collagen. Several generations of dentin bonding systems (DBS) have been studied in the last 20 years. The dentin bond strengths associated with these DBS have been constantly lower than the enamel bond strengths. Recently, a new generation of DBS has been described. They are applied in three steps: an acid agent on enamel and dentin (total etch technique), two mixed primers and a bonding agent based on a methacrylate resin. They are supposed to bond composite resin to wet dentin through dentin organic component, forming a peculiar blended structure that is part tooth and part resin: the hybrid layer.

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Aktivitas Antifungi Air Perasan Bawang Merah (Allium ascalonicum L.) Terhadap Candida albicans Secara In Vitro

Jurnal Ilmu Kedokteran ◽

10.26891/jik.v9i2.2015.71-77 ◽

2017 ◽

Vol 9 (2) ◽

pp. 71

Author(s):

Nurhasanah Nurhasanah ◽

Fauzia Andrini ◽

Yulis Hamidy

Keyword(s):

Candida Albicans ◽

Antifungal Activity ◽

Allium Sativum ◽

Fungicidal Activity ◽

Positive Control ◽

Negative Control ◽

Randomized Design ◽

Significant Difference ◽

Completely Randomized Design

Shallot (Allium ascalonicum L.) has been known as traditional medicine. Shallot which has same genus with garlic(Allium sativum L.) contains allicin that is also found in garlic and has been suspected has fungicidal activity toCandida albicans. It is supported by several researches. Therefore, shallot is suspected has antifungal activity too.The aim of this research was to know antifungal activity of shallot’s water extortion againsts Candida albicans invitro. This was a laboratory experimental research which used completely randomized design, with diffusion method.Shallot’s water extortion was devided into three concentrations, there were 50%, 100% and 200%. Ketoconazole 2%was positive control and aquadest was negative control. The result of this research based on analysis of varians(Anova), there was significant difference between several treatments and was confirmed with Duncan New MultipleRange Test (DNMRT) p<0,05, there was significant difference between 100% shallot’s water extortion with othertreatments, but there was no significant difference between 50% shallot’s water extortion with 200% shallot’s. Theconclusion was shallot’s water extortion had antifungal activity againsts Candida albicans with the best concentration100%, but it was lower than ketoconazole 2%.

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The Comparison of Ostecyte in the Pressure area and Tension area on Tooth Movement Because of Hyperbaric Oxygen Therapy

DENTA ◽

10.30649/denta.v12i1.162 ◽

2018 ◽

Vol 12 (1) ◽

pp. 34

Author(s):

Arya Barahmanta ◽

Muhammad Faizal Winaris ◽

Pambudi Raharjo

Keyword(s):

Hyperbaric Oxygen ◽

Oxygen Therapy ◽

Tooth Movement ◽

Bone Remodelling ◽

Orthodontic Tooth Movement ◽

Negative Control Group ◽

Positive Control ◽

Negative Control ◽

Control Group ◽

Pressure Area

Background: Orthodontic tooth movement is a interaction prosess of resorption and deposition of bone remodeling. Orthodontic tooth movement by mechanical strength causes changes in alveolar bone. Osteocyte is an essential cell to respond bone remodelling. Hyperbaric Oxygen Therapy affects production of osteocyte because it can release Reactive Oxygen Species (ROS) and Nitrid Oxide (NO). Purpose: To determine the difference number of osteocyte in pressure and tension area during tooth movement by adjuvant of Hyperbaric Oxygen 2,4 ATA during 7 days starting on day 8 to day 14. Materials and Methods: This research used Completery Randomized Control Group Post Test Only Design. 36 cavia cobaya (male) were divided into 3 groups randomly : the negative control groups, positive control group, and treatment group. Preparat staining used Hematoxylin Eosin (HE) and calculated on microscop 1000x with 20 field of view. Data analyses used one way ANOVA and LSD test then compared each area by using paired T test. Result: The data showed that the treatment group (P=10,67) tension area has the highest number of osteocyte than negative control group (K-=3,67), positive control (K+=7,42). In the pressure area showed that negative control group (K-=5,00) has the highest than positive control group (K+=3,83) and treatment (P=3,25). Conclusion: Therapy HBO 2,4 ATA 7 days starting on day 8 to day 14 is could increase osteocyte in the tissue to stimulate process of bone remodelling.<pre> </pre>Keywords: Hyperbaric Oxygen, Tooth movement, Bone remodeling, Osteocyte Correspondence: Arya Brahmanta, Department of Orthodonty, Faculty of Dentistry, Hang Tuah University, Arif Rahman Hakim 150, Surabaya, Phone 031-5945864, Email: <a href="mailto:[email protected]">arya.brahmanta@hangtuah.ac.id</a>

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UJI AKTIVITAS HEPATOPROTEKTOR KOMBINASI EKSTRAK ETANOL DAUN PANDAN WANGI (Pandanus amaryllifolius roxb) DAN KAYU MANIS (Cinnamomum burmanii) TERHADAP KADAR MDA YANG DIINDUKSI PARASETAMOL

Jurnal Kesehatan Kusuma Husada ◽

10.34035/jk.v12i1.580 ◽

2020 ◽

pp. 68-73

Author(s):

Yuni Asri Mulatsih Agami ◽

Eka Wisnu Kusuma

Keyword(s):

Oxidative Stress ◽

Ethanol Extract ◽

Optimal Dose ◽

Experimental Methods ◽

Positive Control ◽

Negative Control ◽

Male Rats ◽

Negative Group ◽

Ic50 Value ◽

Dose Combination

Kasus penyakit hati semakin meningkat seiring penggunaan senyawa hepatotoksin salah satunya karena penggunaan parasetamol dengan dosis berlebih. Hal tersebut dapat meningkatkan produksi radikal bebas sehingga memicu terjadinya stress oksidatif yang dapat menimbulkan kerusakan jaringan yang ditandai dengan peningkatan kadar Malondialdehyde (MDA). Stress oksidatif dapat diatasi dengan antioksidan dari berbagai tanaman. Kulit kayu manis memiliki aktivitas antioksidan dengan nilai IC50 53ppm dan daun pandan wangi 39,7% Penelitian ini bertujuan untuk mengetahui aktivitas kombinasi ekstrak etanol daun pandan wangi dan kayu manis dalam menurunkan kadar MDA. tikus yang diinduksi parasetamol. Penelitian menggunakan metode eksperimental, dilakukan selama 9 hari dengan 30 ekor tikus jantan dibagi menjadi 6 Kelompok, yaitu: Normal diberi aquadest, Kontrol Positif diberi silimarin 100 mg/kgBB, Kontrol Negatif diberi CMC-Na 0,05%, serta 3 kelompok lainnya diberi kombinasi ekstrak daun pandan wangi:kayu manis berturut-turut dosis I (25:75), dosis II (50:50), dosis III (75:25). Semua kelompok diinduksi parasetamol 2,5 g/kgBB pada hari ke-7 setelah 30 menit perlakuan, kecuali kelompok normal. Pada hari ke 9 dilakukan pengukuran kadar MDA dengan metode TBARs menggunakan spektrofotometri. Pemberian kombinasi ekstrak etanol daun pandan wangi dan kayu manis dapat menurunkan kadar MDA dengan kombinasi dosis yang paling optimal adalah 75:25 berdasarkan statistik dengan nilai signifikan 0,000<0,05 dibandingkan dengan kelompok negatif. Cases of liver disease have increased with the use of hepatotoxin compounds, one of which is due to the use of paracetamol with excessive doses. This can increase the production of free radicals so that it triggers oxidative stress which can cause tissue damage which is characterized by increased levels of Malondialdehyde (MDA). Oxidative stress can be overcome with antioxidants from various plants. Cinnamomum burmanii has antioxidant activity with IC50 value of 53ppm and Pandanus amarrylifolius 39.7%. This study aims to determine the combined activity of ethanol extract of Pandanus amarrylifolius and Cinnamomum burmanii in reducing MDA levels. Paracetamol-induced rats. Research using experimental methods, conducted for 9 days with 30 male rats divided into 6 groups, namely: Normal given aquadest, Positive Control were given silimarin 100 mg / kgBB, Negative Control was given CMC-Na 0.05%, and 3 other groups were given a combination of Pandanus amarrylifolius extract: Cinnamomum burmanii dose I (25:75), dose II (50:50), dose III (75:25). All groups induced paracetamol 2.5 g / kgBB on the 7th day after 30 minutes of treatment, except the normal group. On the 9th day MDA levels were measured using the TBARs method using spectrophotometry. Giving a combination of Pandanus amarrylifolius and Cinnamomum burmanii ethanol extract can reduce MDA levels with the most optimal dose combination is 75:25 based on statistics with a significant value of 0,000<0.05 compared with the negative group.

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UJI IMUNOMODULATOR DARI EKSTRAK ETANOL DAUN WARU (HIBISCUS TILIACEUS) DENGAN METODE HIPERSENSITIVITAS TIPE LAMBAT

Jurnal Penelitian Farmasi & Herbal ◽

10.36656/jpfh.v1i2.103 ◽

2019 ◽

Vol 1 (2) ◽

pp. 11-16

Author(s):

Yanna Rotua Sihombing ◽

Debi Dinha Sitepu

Keyword(s):

Treatment Group ◽

Leaf Extract ◽

Positive Control ◽

Negative Control ◽

Delayed Type Hypersensitivity ◽

Hypersensitivity Response ◽

Delayed Type Hypersensitivity Response

Immunomodulator is a compound that can increaase the imuno system. One of the plants that have immunomodulator’s activity is Waru Leaf (Hibiscus tiliaceus). the purpose of this research was to test the effect of immunomodulator by extract of Waru Leaf ethanol on rat male. The activity of immunomodulator was determined by using digital pletysmometer by measuring the differences between the last leg swelling’s volume and the first leg swelling’s volume. The treatment group were divided into 5 groups. Each group consistof 5 rats CMC-Na 0,5% (negative control), Stimuno® 32,5 mg/kgBW (positive control), dose of EEDW 50, 100 and 200 mg/kgBW, and bacteria E.coli as antigen. The results slowed that distribution of EEDW dose 200 mg/kgBW can give the effect of immunostimulant by swelling enthancement compared by CMC-Na 0,5 %. EEDW 200 mg/kgBW that have activity comparable with Stimuno® 32,5 mg/kgBW. Thus, it is concluded that of Waru Leaf extract has immunomodulator effects on delayed-type hypersensitivity response of rat male.

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