Vijaya Rathna

Ms. Vijaya Rathna


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 April 2012 in Molecules
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Journal Article
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VRVijaya Rathna
Vijaya Rathna
ZZZuraini Zakaria
Zuraini Zakaria
YCYeng Chen
Yeng Chen
LLLachimanan Yoga Latha
Lachimanan Yoga Latha
JKJagat Kanwar
Jagat Kanwar
SSSreenivasan Sasidharan
Sreenivasan Sasidharan
The urgent need to treat multi-drug resistant pathogenic microorganisms in chronically infected patients has given rise to the development of new antimicrobials from natural resources. We have tested Elaeis guineensis Jacq (Arecaceae) methanol extract against a variety of bacterial, fungal and yeast strains associated with infections. Our studies have demonstrated that E. guineensis exhibits excellent antimicrobial activity in vitro and in vivo against the bacterial and fungal strains tested. A marked inhibitory effect of the E. guineensis extracts was observed against C. albicans whereby E. guineensis extract at ½, 1, or 2 times the MIC significantly inhibited C. albicans growth with a noticeable drop in optical density (OD) of the bacterial culture. This finding confirmed the anticandidal activity of the extract on C. albicans. Imaging using scanning (SEM) and transmission (TEM) electron microscopy was done to determine the major alterations in the microstructure of the extract-treated C. albicans. The main abnormalities noted via SEM and TEM studies were the alteration in morphology of the yeast cells. In vivo antimicrobial activity was studies in mice that had been inoculated with C. albicans and exhibited good anticandidal activity. The authors conclude that the extract may be used as a candidate for the development of anticandidal agent.

1 December 2024 in Non-coding RNA Research
Verified
Journal Article
Open access
SSSumaira Sahreen
Sumaira Sahreen
VRVijaya Rathna
Vijaya Rathna
MHManisekaran Hemagirri
Manisekaran Hemagirri
Mohd AdnanMohd Adnan
Mohd Adnan
Md. Imtaiyaz HassanMd. Imtaiyaz Hassan
Md. Imtaiyaz Hassan
SSSreenivasan Sasidharan
Sreenivasan Sasidharan
Irrespective of medical technology improvements, cancer ranks among the leading causes of mortality worldwide. Although numerous cures and treatments exist, creating alternative cancer therapies with fewer adverse side effects is vital. Since ancient times, plant bioactive compounds have already been used as a remedy to heal cancer. These plant bioactive compounds and their anticancer activity can also deregulate the microRNAs (miRNAs) in the cancerous cells. Therefore, the deregulation of miRNAs in cancer cells by plant bioactive compounds and the usage of the related miRNA could be a promising approach for cancer cure, mainly to prevent cancer and overcome chemotherapeutic side effect problems. Hence, this review highlights the function of plant bioactive compounds as an anticancer agent through the underlying mechanism that alters the miRNA expression in cancer cells, ultimately leading to apoptosis. Moreover, this review provides insight into using plant bioactive compounds -driven miRNAs as an anticancer agent to develop miRNA-based cancer gene therapy. They can be the potential resource for gene therapy and novel strategies targeting cancer therapeutics.

23 November 2012 in Molecules
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Journal Article
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CGChong Grace-Lynn
Chong Grace-Lynn
YCYeng Chen
Yeng Chen
LLLachimanan Yoga Latha
Lachimanan Yoga Latha
JKJagat Kanwar
Jagat Kanwar
SJSubramanion L. Jothy
Subramanion L. Jothy
SSSreenivasan Sasidharan
Sreenivasan Sasidharan
The aim of the present study was to evaluate the hepatoprotective activity of lantadene A against acetaminophen-induced liver toxicity in mice was studied. Activity was measured by monitoring the levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP) and bilirubin, along with histo-pathological analysis. Silymarin was used as positive control. A bimodal pattern of behavioural toxicity was exhibited by the lantadene A-treated group at the beginning of the treatment. However, treatment with lantadene A and silymarin resulted in an increase in the liver weight compared with the acetaminophen treated group. The results of the acetaminophen-induced liver toxicity experiments showed that mice treated with lantadene A (500 mg/kg) showed a significant decrease in the activity of ALT, AST and ALP and the level of bilirubin, which were all elevated in the acetaminophen treated group (p < 0.05). Histological studies supported the biochemical findings and a maximum improvement in the histoarchitecture was seen. The lantadene A-treated group showed remarkable protective effects against histopathological alterations, with comparable results to the silymarin treated group. The current study confirmed the hepatoprotective effects of lantadene A against the model hepatotoxicant acetaminophen, which is likely related to its potent antioxidative activity.

2 September 2015 in Asian Pacific Journal of Cancer Prevention
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Journal Article
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VRVijaya Rathna
Vijaya Rathna
SJSubramanion L Jothy
Subramanion L Jothy
YCYeng Chen
Yeng Chen
JKJagat R Kanwar
Jagat R Kanwar
SSSreenivasan Sasidharan
Sreenivasan Sasidharan
Anti-Cancer Natural Products Inducing Cross-talk between Apoptosis and Autophagy Mutual Proteins to Regulate Cancer Cell Death: Design of Future Green Anticancer Therapies

15 July 2014 in Asian Pacific Journal of Cancer Prevention
Verified
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VRVijaya Rathna
Vijaya Rathna
SSSreenivasan Sasidharan
Sreenivasan Sasidharan
Coaxing Cancer Pro-Apoptoticity: An Approach Blending Therapeutic miRNAs and Dietary Phytochemicals