ISSN 2326-7275
Research Article
International Journal of Anatomy and Physiology ISSN: 2326-7275 Vol. 7 (4), pp. 001-004, April, 2018. © International Scholars Journals
Full Length Research Paper
Volatile constituents and anti candida activity of the aerial parts essential oil of Dittrichia graveolens (L.) Greuter grown in Iran
Nasrin Aghel1*, Ali Zarei Mahmoudabadi2 and Loobat Darvishi1
1Medicinal Plant Research Center, Department of Pharmacognosy, School of Pharmacy, Jundishapour Medical Sciences University, Ahwaz, Iran.
2Infectious and Tropical Diseases Research Center, Department of Medical Mycology, School of Medicine, Jundishapour Medical Sciences University, Ahwaz, Iran.
Accepted 30 May, 2017
Abstract
The aims of present study were to analysis of chemical compositions and evaluate anti-Candida activity of Dittrichia gravolence essential oil. The composition of the hydrodistilled essential oil from aerial parts of D. graveolens (L.) Greuter were grown in Iran investigated by gas chromatography-mass spectroscopy (GC/ MS). The major components, among the identified 22, were 1,8 Cineol (54.89%), P-Cymen (16.2%), [beta]-pinene (6.94%) and Borneol (5.44%) . Anti-Candida activity of the volatile oil of the aerial parts of D. gravolence against different isolates of Candida albicans was studied in vitro. Anti-Candida activity was done using serial dilutions of volatile oil in Sabouraud’s dextrose agar (SDA). Agar well diffusion methods was used for detection minimum inhibitory concentration (MIC). MIC for 10 isolates of tested yeasts was 30.675 mg/ml.
Key words: Dittrichia graveolens, essential oil, 1,8 Cineol, Candida albicans.
Nasrin Aghel*, Ali Zarei Mahmoudabadi and Loobat Darvishi
Research Article
Antifungal, cytotoxic activities and docking studies of 2,5-dimercapto-1,3,4-thiadiazole derivatives
International Journal of Anatomy and Physiology ISSN: 2326-7275 Vol. 7 (4), pp. 001-009, April, 2018. © International Scholars Journals
Full Length Research Paper
Antifungal, cytotoxic activities and docking studies of 2,5-dimercapto-1,3,4-thiadiazole derivatives
Weerasak Samee1* and Opa Vajragupta2
1Department of Pharmaceutical Chemistry and Pharmacognosy, Faculty of Pharmacy, Srinakharinwirot University,
Nakhon-nayok, Thailand.
2Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
Accepted 20 September, 2017
Abstract
A series of 2,5-dimercapto-1,3,4-thiadiazole derivatives (compounds 1 to 10) were prepared by nucleophilic substitution reaction between 2,5-dimercapto-1,3,4-thiadiazole and chloroheterocyclic compounds in methanol and in the presence of potassium carbonate (compounds 1 to 5 and 8) or metallic sodium (compounds 6, 7, 9 and 10) at room temperature. The cytotoxic activity was determined by green fluorescent protein (GFP)-based assay and anti-candida activity was determined by resazurin microplate assay (REMA). Compounds 1 to 4, 8 and 9 showed in vitro cytotoxic activities against Vero cells (African green monkey kidney). Compounds 4 and 10 exhibited anti-candida activities against Candida albicans (ATCC 90028) with IC50 values of 1.94 and 19.10 µg/ml, respectively. Docking studies on the catalytic site of cytochrome P450 14a-demethylase were used to identify the chemical structures in the molecule responsible for cytotoxic and anti-candida activities of the synthesized compounds.
Key words: 2,5-dimercapto-1,3,4-thiadiazol, docking, cytotoxicity, antifungal.
Opa Vajragupta, Weerasak Samee*
Research Article
A systematic review of the adverse effects of tacrolimus in organ transplant patients
International Journal of Anatomy and Physiology ISSN: 2326-7275 Vol. 7 (3), pp. 001-008, March, 2018. © International Scholars Journals
Full Length Research Paper
A systematic review of the adverse effects of tacrolimus in organ transplant patients
L. K. Teh1, S. H. M. Dom1, Z. A. Zakaria2 and M. Z. Salleh1*
1Pharmacogenomics Centre (PROMISE), Level 6, FF3, Faculty of Pharmacy, Universiti Teknologi MARA, 42300 Puncak Alam, Selangor, Malaysia.
2Department of Biomedical Science, Faculty of Medicine and Health Sciences, University Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
Accepted 15 April, 2017
Abstract
Tacrolimus has been the drug of choice for prevention of graft rejection following organ transplantations. This systematic review and meta-analysis [UiTM1] was conducted to evaluate the efficacy of tacrolimus in organ transplantation. Publication in English of randomized clinical trials, which used tacrolimus to prevent graft rejection in adult patients were included in this analysis. Articles were searched from PubMed, Science Direct, Blackwell and Ovid Gateway, which were published since 1980 to 2007. The outcomes measured were biopsy-proven acute rejection at three months; graft survival at one year; post-transplant diabetes mellitus; hypertension and neurotoxicity. Seven reports, which involved 2415 participants showed that tacrolimus was associated with reduced odds of biopsy-proven acute rejections three months of post-transplantation (pooled odds ratio of 0.69; 95% CI 0.49 to 0.96) and improved graft survival at one year (pooled odds ratio of 1.11 and 95% confidence interval 0.72 to 1.71). In terms of adverse effects, tacrolimus-treated patients were significantly at high odds of developing post-transplant diabetes mellitus (pooled odds ratio of 1.90; 95% CI 1.09 to 3.30) and neurotoxicity (pooled odds ratio of 1.61; 95% CI 1.15 to 2.25) but reduced odds of developing hypertension (pooled odds ratio of 0.80; 95% CI 0.65 to 0.98). Low to moderate heterogeneity between trials existed for the incidences of biopsy-proven acute rejections, graft survival, post-transplant diabetes mellitus and incidence of hypertension; but the analysis showed a significant increment of neurotoxicity by tacrolimus.
Key words: Tacrolimus, neurotoxicity, hypertension, diabetes mellitus, efficacy.
S. H. M. Dom, Z. A. Zakaria and M. Z. Salleh*, L. K. Teh
Research Article
Antioxidant activities of phenolic components from various plants of Desmodium species
International Journal of Anatomy and Physiology ISSN: 2326-7275 Vol. 7 (3), pp. 001-010, March, 2018. © International Scholars Journals
Full Length Research Paper
Antioxidant activities of phenolic components from various plants of Desmodium species
Jen-Chieh Tsai1, Guan-Jhong Huang2, Tai-Hui Chiu1, Shyh-Shyun Huang2, Shun-Chieh Huang1, Tai-Hung Huang1, Shang-Chih Lai3 and Chao-Ying Lee1*
1School of Pharmacy, College of Pharmacy, China Medical University, Taichung, Taiwan, Republic of China.
2Graduate Institute of Chinese Pharmaceutical Sciences, College of Pharmacy, China Medical University, Taichung, Taiwan, Republic of China.
3Department of Health and Nutrition Biotechnology, College of Health Science, Asia University, Taichung, Taiwan, Republic of China.
Accepted 10 April, 2017
Abstract
The aim of this study was to examine the antioxidant activities and phenolic components of the crude extracts of 10 Desmodium species from Taiwan. In this study, DPPH free radical scavenging activity, ABTS radical monocation scavenging activity, ferric-reducing antioxidant power (FRAP) and reducing power of the 10 Desmodium species were evaluated for their antioxidant activities. The results showed that, of all the samples, Desmodium sequax was the most active in ABTS, DPPH, FRAP and reducing power assays. The total polyphenol, total flavonoid and total flavonol contents of the crude extract were calculated. The correlation coefficient (R2) values of TEAC with phenolic compounds indicated strong positive correlations, except for total flavonoid content. Furthermore, HPLC chromatographic fingerprints were established, and chlorogenic acid and vitexin in D. sequax were quantified. Chlorogenic acid was confirmed to express strong antioxidant activities in ABTS, DPPH, FRAP and reducing power assays. The present study indicated the antioxidant activities of the 10 Desmodium species were related to their phenolic components. D. sequax is a potent antioxidant medicinal plant, and chlorogenic acid may be an important factor in the antioxidant activity of this plant.
Key words: Desmodium, antioxidant activity, chlorogenic acid, vitexin.
Shyh-Shyun Huang, Shang-Chih Lai and Chao-Ying Lee*, Shun-Chieh Huang, Tai-Hung Huang, Tai-Hui Chiu, Guan-Jhong Huang, Jen-Chieh Tsai
Research Article
International Journal of Anatomy and Physiology ISSN: 2326-7275 Vol. 7 (2), pp. 001-009, February, 2018. © International Scholars Journals
Full Length Research Paper
Preventive effect of Rhododendron arboreum on cardiac markers, lipid peroxides and antioxidants in normal and isoproterenol-induced myocardial necrosis in rats
Manjunatha P. Mudagal*, Sandip Karia and Divakar Goli
Department of Pharmacology, Acharya and B. M. Reddy College of Pharmacy, Soladevanahalli, Chikkabanavara Post, Bangalore- 560090, Karnataka, India.
Accepted 21 April, 2017
Abstract
This study was designed to investigate the preventive effect of ethanolic extract of Rhododendron arboretum (ERA) against isoproterenol-induced myocardial ischemia in rat myocardium. Wister rats were pretreated with ERA (100, 250, 500 mg kg-1) orally for 42 days and then intoxicated with isoproterenol (ISO, 150mg/kg body weight, s.c. for 2 days). MI induced in rats by subcutaneous injection of ISO-(150 mg/kg body weight) at interval of 24 h for 2 days showed significant elevation in serum cardiac marker enzymes like lactate dehydrogenase (LDH), aspartate transaminase (AST) and alanine transaminase (ALT) . Lipid peroxidative product like lipid hydroperoxidase was elevated in tissue and serum, decline in enzymatic antioxidant status (superoxide dismutase, catalase, glutathione peroxidase) and non-enzymatic reduced glutathione antioxidants. Pretreatment with ERA to ISO-treated rats caused a significant protective effect. Administration of ERA in normal rats did not have any significant effect on cardiac markers, lipid peroxidation and antioxidant levels. The results of our study show that ERA possesses protective effect result from suppression of oxidative stress in ISO-induced myocardial infracted rats. Histopathological examination further confirmed the cardioprotective effect of ERA against ischemic insult.
Key words: Myocardial infarction, isoproterenol, antioxidants, Rhododendron arboreum, oxidative stress.
Manjunatha P. Mudagal*, Sandip Karia and Divakar Goli
Research Article
Antioxidant and antibacterial constituents from Morus nigra
International Journal of Anatomy and Physiology ISSN: 2326-7275 Vol. 7 (1), pp. 001-004, January, 2018. © International Scholars Journals
Full Length Research Paper
Antioxidant and antibacterial constituents from Morus nigra
Ofentse Mazimba1*, Runner R. T. Majinda1 and Daniel Motlhanka2
1Department of Chemistry, University of Botswana, Private Bag 00704, Gaborone, Botswana.
2Department of Basic Sciences, Botswana College of Agriculture, Private Bag 0027, Gaborone, Botswana.
Accepted 27 May, 2017
Abstract
The objective of this study was to isolate and characterize the constituents of the local Morus nigra L. (Black mulberry), to compare its constituents with other studied Mulberries and to evaluate its anti-oxidative and anti-bacterial activities. The isolated compounds were identified by comparison of spectral data (UV, IR, MS and NMR) with literature values. The stem bark and wood of M. nigra yielded a stilbenoid oxyresveratrol 1, a 2- arylbenzofuran moracin M2, four isoprenylated flavonoids; cyclomorusin 3, morusin 4, kuwanon C5 and a derivative of kuwanon C6, two tritepenes; betulinic acid 7, -amyrin acetate 8 and a steroidal saponin -sitosterol-3-O- -D- glucoside 9. The phenolic isolates showed moderate DPPH radical scavenging activity (EC50 = 23-135 µgml-1) compared to ascorbic acid (EC50 = 41 µgml-1) after 30 min. Compounds 1, 2 and 4 to 6 showed activities against Staphylococcus aureus, Bacillus subtilis, Micrococus flavus, Streptococcus faecalis, Salmonella abony, Pseudomonas aeruginosa.
Key words: Morus nigra, antioxidant, antibacterial, oxyresveratrol, isoprenylated flavonoids.
Runner R. T. Majinda and Daniel Motlhanka, Ofentse Mazimba*