The in vitro study of anti-leishmanial effect of Naja naja oxiana snake venom on Leishmania major

Author(s):  
Nastaran Fallahi ◽  
Delavar Shahbazzadeh ◽  
Fatemeh Maleki ◽  
Marjaneh Aghdasi ◽  
Fatemeh Tabatabaie ◽  
...  

Background: Although a majority of patients with cutaneous leishmaniasis (CL) are healed with Glucantime chemotherapy, the increased drug resistance rate following its consumption is a concern. In this study , Naja naja oxiana crude venom of cobra snakes was used for the first time as an assembled combination of bioactive pharmaceutical components on Leishmania major (L. major) standard strain . Objective: To evaluate the efficacy of the Naja naja oxiana crude venom of Iranian cobra snakes on Leishmania major standard strain in vitro. Methods: Five concentrations (1.25, 2.5, 5, 10 and 20 µg/mL) of venom were added to Leishmania major cultures at 24, 48 and 72 h. The viability of the parasites and venom toxicity were assessed by MTT test. The apoptosis was determined by flowcytometry, while IC50 was determined by counting parasites compared to that of glucantime. Each test was conducted in triplicate. Results: After exposure the venom at 2.5 µg/mL for 72 h, IC50 value was 0.36 µg/mL and 14.12 µg/mL for promastigotes and amastigotes, respectively. MTT valuation clarified 1.01% promastigotes viability. Furthermore, the results indicated that the venom of Naja naja oxiana induced early and late apoptosis in parasites. Conclusions: The venom of Naja naja oxiana revealed remarkable anti-leishmanial effects as a novel anti-parasitic alternative. Thus the bioactive and effective fractions of this venom may be considered as anti-leishmanial candidates in future studies.

2014 ◽  
Vol 9 (1) ◽  
Author(s):  
K. V. N. Rathnakar Reddi ◽  
Sivarathri Siva Rajesh ◽  
Kumara Narendra ◽  
Swathi Jangala ◽  
Puli Chandra Obul Reddy ◽  
...  

2004 ◽  
Vol 845 ◽  
Author(s):  
Ai Lin Chun ◽  
Hicham Fenniri ◽  
Thomas J. Webster

ABSTRACTOrganic nanotubes called helical rosette nanotubes (HRN) have been synthesized in this study for bone tissue engineering applications. They possess intriguing properties for various bionanotechnology applications since they can be designed to mimic the nanostructured constituent components in bone such as collagen fibers and hydroxyapatite (Ca5(PO4)3(OH)) which bone cells are naturally accustomed to interacting with. This is in contrast to currently used orthopaedic materials such as titanium which do not possess desirable nanometer surface roughness. The objective of this in vitro study was to determine bone-forming cell (osteoblasts) interactions on titanium coated with HRNs. Results of this study showed for the first time increased osteoblast adhesion on titanium coated with HRNs compared to those not coated with HRNs. In this manner, this study provided evidence that HRNs should be further considered for orthopaedic applications.


2016 ◽  
Vol 41 (2) ◽  
pp. 375-379 ◽  
Author(s):  
Mohammad Hossein Motazedian ◽  
Fattaneh Mikaeili ◽  
Mehdi Mohebali ◽  
Ramin Miri ◽  
Parvaneh Habibi ◽  
...  

Author(s):  
Rochmah Kurnijasanti ◽  
Amaq Fadholly

Capsicum annum L. is a potential natural plant that have a lot of various pharmacological effects, including as anticancer agent. This study Aim to analyze Capsicum annum extract (CAE) on T47D cells. CAE (10, 20, 40, 60, 80µg/mL) treated on T47D cells to determined IC50 value by MTT assay. Apoptosis induction is also investigated through caspase-3 expressions (IC50, 2IC50). The present study showed that CAE suppress T47D cells proliferation with IC50 value of 75.81µg/mL. The caspase-3 expression on 2IC50 is higher (67.16%) than IC50 (52.16%). This result indicate that CAE has ability as anticancer agent by inhibiting cell growth and induce apoptosis through caspase-3 expression on T47D cells. Further study of CAE holds potential for novel therapies of cancer prevention and treatment.


2021 ◽  
Vol 13 (2) ◽  
pp. 47-51
Author(s):  
Samaneh Abbasi ◽  
Soodabe Ebrahimi ◽  
Arash Shisheian ◽  
Maryam Farhadian

Background: Acrylic resin teeth wear resistance has an important role in the denture longevity. This study aimed to clarify the effect of glaze coating on wear resistance of three types of artificial acrylic teeth. Methods: In this in vitro study, the wear resistance rate of three of acrylic denture teeth (GENIUS, STON and CLASSIC) was compared with Ivoclar teeth (n=25/group). The wear resistance was measured by estimating the weight loss in pre and post removing glaze coating, following 5000 cycles in the chewing simulator device. Data analysis was made using paired t test, one-way ANOVA and Tukey’s post hoc test. Results: ANOVA test showed that there was no significant difference between the mean amount of wear of GENIUS, CLASSIC, STON and IVOCLAR teeth in the first stage (P <0.061), but this difference was significant (P <0.001) in the second stage. The result of Tukey post hoc test showed that wear rates of GENIUS were significantly lower than other groups (P<0.001). Comparison between the mean wear rates of each dental group at the first and second stages showed a significant difference between average teeth wear resistance of CLASSIC, STON and IVOCLAR in the first and second stages (P <0.001). Conclusions: In conclusion, the teeth wear resistance of STON and CLASSIC were similar to IVOCLAR. Also, after removing the glaze coating, the teeth wear resistance decreased in all groups but was not statistically significant for group GENIUS.


2019 ◽  
Vol 7 (22) ◽  
pp. 3816-3818
Author(s):  
Nadiya Anandita Nasution ◽  
Urip Harahap ◽  
Ginda Haro ◽  
Hari Purnomo ◽  
Denny Satria

AIM: The aim of this study was to determine cytotoxic activity of BornUSU I or Boronhafagama I (1,5-bis(4-hydroxyphenyl)-3-oxa-1,5-diaza-2,4-diboropentane-2,4-diol) as a boron derivate compounds which are boron neutron captured theraphy (BNCT) candidates. METHODS: The T47D cells were treated by BornUSU I, and Tamoxifen as a positive control. The in vitro study was using MTT method with the incubation period for 24h and 48h. All data were determined using viability of cells equation for showing each IC50 value. RESULTS: The IC50 value of BornUSU I and Tamoxifen were 72.61 ± 0.82 µM and 10.62 ± 0.06 µM for 24 h incubation period, and for the 48 h incubation period were 44.63 ± 0.23 µM and 7.79 ± 0.05 µM. The 48 h incubation period results showed the lowest IC50 value. CONCLUSION: The results reveal that BornUSU I provide effective as anticancer, especially for breast cancer treatment.


2008 ◽  
Vol 32 (1) ◽  
pp. 214-222
Author(s):  
S. A.G. Al-Samarrae

This study was carried out to evaluate the ability of Lactobacillusacidophilus to prevent and treat Salmonella typhimurium in puppies. In vitroantibiotic sensitivity test of S. typhimurium was made and the result revealedthat Ciprofloxacin is the most effective.Isolation of L. acidophilus from theintestinal tract of the normal dogs and also revealed that all Lactobacillus strainswere biochemically identical to standard strain. A bacterial strain that had highability to inhibit the growth of S. typhimurium in vitro with high ability toadhere to intestinal epithelial cells and tolerate the low pH and bile salts waschosen for the experimental study.Twenty puppies were divided into four groups and treated in different ways.The clinical, haematological and biochemical parameters were obtained from allanimals at the period of two days before inoculation until the death of animals ofthe first group at the sixth day post infection. The results revealed that , puppiesexperimentally infected with S.typhimurium showed both septicemic andgastrointestinal forms of the disease accompanied with isolation ofS.typhimurium from the blood and stool throughout the experiment. Thestatistical analysis of the results of all parameters among all groups revealed ,forthe first time, that L.acidophilus plays an important role in the prevention ofS.typhimurium infection in puppies . It also has high therapeutic effect againstS.typhimurium, which was almost similar to that of Ciprofloxacin.


2021 ◽  
Vol 7 (2) ◽  
pp. 95-98
Author(s):  
Zakia Jahan ◽  
Masudul Hassan

The Coronavirus disease 2019 (COVID-19) outbreak, forcing us to face unprecedented moments in the world. The huge devastating impact of the world due to the covid-19 attack causes the brink of no return. However, there is no proven and specific treatment for Covid -19. Very few medications have received Emergency Use of Authorization. A recent in vitro study was the first time to find out and to assess the antiviral effect of Ivermectin on COVID-19. The study showed that Ivermectin was active against COVID- 19-infected cells, was able to kill effectively almost all viral particles within 48 h. In these moments of crisis, FDA-approved ivermectin is a ray of hope. Bangladesh Journal of Infectious Diseases 2020;7(2):95-98


2020 ◽  
Vol 12 (2) ◽  
pp. 171-177
Author(s):  
Alisha Akya ◽  
Roya Chegene Lorestani ◽  
Hossein Zhaleh ◽  
Fatemeh Nemati Zargaran ◽  
Keyghobad Ghadiri ◽  
...  

Author(s):  
Jagadish Rajkumaar R ◽  
Anitha Roy ◽  
Lakshmi T

Objective: The aim of the present study was to analyze the effect of the aqueous fruit pulp extract of Tamarindus indica L. (tamarind extract) on cytochrome P 450 isoform CYP3A4.Methods: Tamarind extract at different concentrations from 5 to 100 μg/ml was examined for its inhibitory property toward cytochrome P 450 isoform CYP3A4. The various concentrations of tamarind extract, potassium phosphate buffer, CYP450 reagent, and substrate 7-Benzyloxy-4- trifluoromethylcoumarin were added to a 96-well plate. The mixtures were preincubated for 20 min at room temperature. The reaction was started by a mixture of free constituted substrate and NADP+ and incubated at room temperature for 30–60 min. The reaction was stopped by Tris-HCl buffer, pH 10.5. The fluorescent intensities of the products were measured by PerkinElmer Enspire fluorescence reader using an excitation and emission wavelength of 405 nm and 460 nm, respectively. Inhibitory concentration (IC50) was calculated by plotting concentrations of tamarind extract against the corresponding percentage inhibition.Results: All the tested concentrations of extract except 5 μg/ml showed good inhibition against CYP3A4 in a dose-dependent manner. The IC50 value of tamarind for CYP3A4 inhibitory activity was found to be 27.89 μg/ml.Conclusion: T. indica aqueous fruit pulp extract exhibited an inhibitory effect on CYP34A, thereby indicating the possibilities of herb-drug interaction if these extracts are coadministered with the prescribed drugs that are metabolized by CYP3A4.


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