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Dive into the research topics where Dipak Kumar is active.

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Featured researches published by Dipak Kumar.


Scientific Reports | 2016

Differential responses of Trans -Resveratrol on proliferation of neural progenitor cells and aged rat hippocampal neurogenesis

Vivek Kumar; Ankita Pandey; Sadaf Jahan; Rajendra Kumar Shukla; Dipak Kumar; Shripriya Singh; C. S. Rajpurohit; Sanjay Yadav; Vinay K. Khanna; Aditya Bhushan Pant

The plethora of literature has supported the potential benefits of Resveratrol (RV) as a life-extending as well as an anticancer compound. However, these two functional discrepancies resulted at different concentration ranges. Likewise, the role of Resveratrol on adult neurogenesis still remains controversial and less understood despite its well documented health benefits. To gather insight into the biological effects of RV on neurogenesis, we evaluated the possible effects of the compound on the proliferation and survival of neural progenitor cells (NPCs) in culture, and in the hippocampus of aged rats. Resveratrol exerted biphasic effects on NPCs; low concentrations (10 μM) stimulated cell proliferation mediated by increased phosphorylation of extracellular signal-regulated kinases (ERKs) and p38 kinases, whereas high concentrations (>20 μM) exhibited inhibitory effects. Administration of Resveratrol (20 mg/kg body weight) to adult rats significantly increased the number of newly generated cells in the hippocampus, with upregulation of p-CREB and SIRT1 proteins implicated in neuronal survival and lifespan extension respectively. We have successfully demonstrated that Resveratrol exhibits dose dependent discrepancies and at a lower concentration can have a positive impact on the proliferation, survival of NPCs and aged rat hippocampal neurogenesis implicating its potential as a candidate for restorative therapies against age related disorders.


Annals of Ophthalmology | 2004

Impaired anti-oxidant defense mechanism in central eales disease

Sandeep Saxena; Dipak Kumar; Vinay K. Khanna; Prachi Srivastava; Prahlad K. Seth

A tertiary care center-based, case-control study evaluated the status of oxidative stress, enzymes involved in the antioxidant defense and membrane fluidity in platelets of 6 cases with central Eales disease and 5 healthy controls. Significant differences were observed between malonaldialdehyde, superoxide dismutase and catalase levels in the cases and controls. Enhanced oxidative stress, is consistent with an emerging view that antioxidant defenses decline in association with the disease process.


Annals of Ophthalmology | 2005

The topographic distribution of retinal neovascularization in Eales’ disease

Sandeep Saxena; Dipak Kumar

Topographic distribution of retinal neovascularization in 66 cases of Eales’ disease was studied. Neovascularization of the optic disc (NVD), neovascularization elsewhere (NVE), and combined NVD and NVE were observed in 16 (21.1%), 52 (68.4%), and 8 (10.5%) eyes, respectively. Quadrantic distribution of NVE were superotemporal, 46%; inferotemporal, 24.3%; superonasal, 16.2%; and inferonasal, 13.5%. This information should influence retinopathy monitoring in Eales’ disease.


Scientific Reports | 2018

Discovery of Novel Soluble Epoxide Hydrolase Inhibitors as Potent Vasodilators

Neetika Tripathi; Sarvesh Paliwal; Swapnil Sharma; Kanika Verma; Ritika Gururani; Akanksha Tiwari; Amrita Verma; Monika Chauhan; Aarti Singh; Dipak Kumar; Aditya B. Pant

In view of the role of sEH (soluble epoxide hydrolase) in hypertension, we have developed a rigorously validated pharmacophore model containing one HBA (Hydrogen Bond Acceptor), two HY (Hydrophobic) and one RA (Ring Aromatic) features. The model was used as a query to search the NCI (National Cancer Institute) and Maybridge database leading to retrieval of many compounds which were sorted on the basis of predicted activity, fit value and Lipinski’s violation. The selected compounds were docked into the active site of enzyme soluble epoxide hydrolase. Potential interactions were observed between the features of the identified hits and the amino acids present in the docking site. The three selected compounds were subjected to in vitro evaluation using enzyme- based assay and the isolated rat aortic model followed by cytotoxicity studies. The results demonstrate that the identified compounds are potent, safe and novel soluble epoxide hydrolase inhibitors.


Current Medicinal Chemistry | 2017

Therapeutic Targeting of NLRP3 Inflammasomes by Natural Products and Pharmaceuticals: A Novel Mechanistic Approach for Inflammatory Diseases

Sadaf Jahan; Dipak Kumar; Swati Chaturvedi; Mamunur Rashid; Muhammad Wahajuddin; Yasir A. Khan; Sameer N. Goyal; Chandragouda R. Patil; Rajesh Mohanraj; Sandeep Subramanya; Shreesh Ojha

Inflammasomes are multiprotein complexes having nucleotide-binding domain and leucine-rich repeat consisting members along with pyrin and HIN domain family. An inflammasome mainly consists of cytoplasmic sensor molecule, such as NLRP3, the adaptor apoptosisassociated speck-like protein containing caspase recruitment domain) protein along with effector procaspase-1. The inflammasome regulates caspase-1 activation, resulting in secretion of interleukin- 1β and interleukin-18. The inflammasome activation is linked with infection, stress, or other immunological signals involved in inflammation. The pathophysiological role of NLRP3 inflammasome in immune regulation, inflammatory receptor-ligand interactions, microbial-associated molecular patterns, danger as well as pathogen associated molecular patterns has been demonstrated in last few years. Furthermore, the role of the inflammasome in peripheral and central nervous system involved with cytokine and chemokine inflammatory responses has been demonstrated in preclinical and clinical studies. The understanding of molecular regulation of inflammasome associated pathways is crucial for drug design and delivery. The use of natural product as an alternate therapy is gaining focus because of easy access and cost effectiveness. A number of herbal extracts and its bioactive constituents known as phytochemicals have shown to be effective in inflammatory response mediated by NLRP3 inflammasomes pathways. To understand the interaction of phytochemicals and inflammasome at the molecular level, it is vital to develop effective drugs that can be evaluated further in the clinical settings. Therefore, this review renders an extensive account of all the phytochemicals which are evaluated either in inflammatory experimental animal models or in immortalized human/animal cell lines that modulate NLRP3 inflammasome mediated pathways to mitigate inflammatory responses with the hope that this pathway modulation by phytochemicals may provide a another class of drugs in the armamentarium as well as novel molecular mechanism of natural products targeting NLRP3 inflammasome.


Annals of Ophthalmology | 2001

Enhanced oxidative stress in eales disease

Sandeep Saxena; Vinay K. Khanna; Dipak Kumar; Prachi Srivastava; Prahlad K. Seth


Indian Journal of Ophthalmology | 2000

Management of diabetic retinopathy

Sandeep Saxena; Subhadra Jalali; Travis A. Meredith; Nancy M. Holekamp; Dipak Kumar


Annals of Ophthalmology | 2000

Macular involvement in eales disease

Sandeep Saxena; Dipak Kumar


Molecular Vision | 2005

Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.

Vedam Lakshmi Ramprasad; Sarangapani Sripriya; George Ronnie; Derek J. Nancarrow; Sandeep Saxena; Arvind Hemamalini; Dipak Kumar; Lingam Vijaya; Govindasamy Kumaramanickavel


Annals of Ophthalmology | 2002

C-reactive protein in Eales disease

Sandeep Saxena; Dipak Kumar; Sangeeta Kapoor; Amita Jain

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Vinay K. Khanna

Indian Institute of Toxicology Research

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Prahlad K. Seth

Indian Institute of Toxicology Research

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Sadaf Jahan

Indian Institute of Toxicology Research

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Aditya B. Pant

Indian Institute of Toxicology Research

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Aditya Bhushan Pant

Indian Institute of Toxicology Research

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