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Dive into the research topics where Dev Karan is active.

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Featured researches published by Dev Karan.


Biomedicine & Pharmacotherapy | 2003

Immunomodulatory effects of agents of plant origin

Lilly Ganju; Dev Karan; Sudipta Chanda; K.K. Srivastava; R. C. Sawhney; W. Selvamurthy

The immunomodulatory properties of amla (Emblica officinalis) and shankhpushpi (Evolvulus alsinoides) were evaluated in adjuvant induced arthritic (AIA) rat model. Injecting Complete Freunds Adjuvant (CFA) in right hind paw of the animals induced inflammation. The crude extracts of both the herbs were administered intraperitonially following a repeated treatment profile. The anti-inflammatory response of both the extracts was determined by lymphocyte proliferation activity and histopathological severity of synovial hyperplasia. Both the extracts showed a marked reduction in inflammation and edema. At cellular level immunosuppression occurred during the early phase of the disease. There was mild synovial hyperplasia and infiltration of few mononuclear cells in amla or shankhpushpi treated animals. The induction of nitric oxide synthase (NOS) was significantly decreased in treated animals as compared to controls. These observations suggest that both the herbal extracts caused immunosuppression in AIA rats, indicating that they may provide an alternative approach to the treatment of arthritis.


Phytomedicine | 2008

EFFECT OF HIPPOPHAE RHAMNOIDES LEAF EXTRACT AGAINST DENGUE VIRUS INFECTION IN HUMAN BLOOD-DERIVED MACROPHAGES

Monika Jain; Lilly Ganju; A. Katiyal; Y.S. Padwad; Kshipra Mishra; Sudipta Chanda; Dev Karan; K.M.S. Yogendra; R. C. Sawhney

Dengue virus occurs as four distinct serotypes, called Dengue 1, 2, 3, and 4. Symptomatic dengue virus infection ranges from a self limited febrile illness, dengue fever (DF), to a more severe disease, dengue hemorrhagic fever/dengue shock syndrome (DHF/DSS). The anti-Dengue treatment is severely hampered as no specific therapeutic agents are available. Even present treatment strategies for Dengue are more supportive than curative. In the present study anti-dengue activity of Hippophae rhamnoides (Seabuckthorn, SBT) leaf extract was evaluated in Dengue virus type-2 infected blood-derived human macrophages as macrophages are the primary target of Dengue virus infection. Infected cells were treated with SBT leaf extract and compared with commercially available anti-viral drug, Ribavirin. The extract was able to maintain the cell viability of Dengue-infected cells at par with Ribavirin along with the decrease and increase in TNF-alpha and IFN-gamma respectively. Anti-dengue activity of SBT extract was further determined by the traditional plaque assay. These observations suggest that the SBT leaf extract has a significant anti-dengue activity and has the potential for the treatment of Dengue.


Immunopharmacology and Immunotoxicology | 2006

Aqueous Extract of Rhodiola imbricata Rhizome Stimulates Proinflammatory Mediators via Phosphorylated IκB and Transcription Factor Nuclear Factor-κB

K.P. Mishra; Y.S. Padwad; Monika Jain; Dev Karan; Lilly Ganju; R. C. Sawhney

Modulation of immune response to alleviate diseases has long since been of interest. Plant extracts have been widely investigated for their possible immunomodulatory properties. We have evaluated the immunomodulatory activity of aqueous extract of Rhodiola rhizome in human peripheral blood mononuclear cells (PBMCs) and mouse macrophage cell line RAW 264.7. The Rhodiola extract was found to stimulate production of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) in human PBMCs as well as RAW 264.7 cell line. It also increased production of nitric oxide synergistically in combination with lipopolysaccharide (LPS) in RAW 264.7. Rhodiola at 250 μg/ml increased the p-IκB expression in human PBMCs. Aqueous extract of Rhodiola (250 μg/ml) also activated the nuclear translocation of NF-κB in human PBMCs, which is comparable to the positive stimulant LPS. Thus, our present study suggests that Rhodiola most likely activates proinflammatory mediators via phosphorylated inhibitory kB and transcription factor NF-kB. Our study demonstrates immunostimulatory potential of aqueous extract of Rhodiola rhizome, that can be used for upregulation of immune response in patients with inadequate functioning of the immune system.


Phytotherapy Research | 2008

Effect of Seabuckthorn (Hippophae rhamnoides) flavone on immune system: an in-vitro approach.

K.P. Mishra; Sudipta Chanda; Dev Karan; Lilly Ganju; R. C. Sawhney

There are several reports, which suggest that the consumption of foods rich in flavonoids is associated with a lower incidence of certain degenerative diseases, including cardiovascular disease. Flavones, of Seabuckthorn (SBT) (Hippophae rhamnoides L.) fruit berry can modulate the production and level of several signaling molecules associated with immune function and inflammation in vitro, including several cytokines. We have evaluated the immunomodulatory activity of ethanolic solution of SBT flavone (FLV) in human peripheral blood mononuclear cells (PBMCs). The SBT flavone was found to stimulate production of interleukin‐6 (IL‐6) and tumor necrosis factor‐α (TNF‐α) in PBMCs. However, increased expressions of p‐IκB, NF‐κB, and p‐p38 were found in flavone‐treated human PBMCs with significantly suppressed expression of CD25 (IL‐2R). There was no alteration found in the nitric oxide (NO) production in mouse macrophage cell line RAW 264.7. These observations suggest that stimulation of IL‐6 and TNF‐alpha secretion may contribute to the putative beneficial effects of dietary flavone against microbial infection. Copyright


Immunobiology | 2009

RNA interference mediated silencing of Hsp60 gene in human monocytic myeloma cell line U937 revealed decreased dengue virus multiplication

Y.S. Padwad; Kshipra Mishra; Monika Jain; Sudipta Chanda; Dev Karan; Lilly Ganju

Heat shock proteins (Hsps) or stress proteins are highly conserved molecules and expressed in all cell types under stressful conditions like heat, cold, hypoxia and infections. The objective of the present study was to determine the effect of dengue virus infection on relative expression of stress proteins and their role in the progression of the infection. As macrophages are the primary host for dengue, human promonocytic myeloblastoma U937 cells were infected with dengue virus type 2 New Guinea C strain for the evaluation of Hsps expression. A significant expression of Hsp60 was observed in virally infected U937 cells as compared to controls. In order to determine the correlation between Hsp60 expression and viral multiplication in infected cells, expression of Hsp60 was down regulated by RNA interference. Viral multiplication was determined by quantification of viral RNA copy number using Real Time PCR and plaque formation assay in cellular supernatants of Hsp60 silenced cells. Intracellular quantification of viral load was also determined by flow cytometry. It was observed that down regulation of Hsp60 in virally infected cells resulted into decrease in viral RNA copy number, plaque forming units and intracellular viral load. At the same time down regulation also resulted in increased IFN-alpha level. These observations suggest that, elevated levels of Hsp60 expression in virally infected cells may help in viral multiplication and could be possible therapeutic targets for the management of dengue virus infection.


Immunobiology | 2009

Aqueous extract of Rhodiola imbricata rhizome stimulates Toll-like receptor 4, granzyme-B and Th1 cytokines in vitro

K.P. Mishra; Lilly Ganju; Sudipta Chanda; Dev Karan; R. C. Sawhney

Rhodiola imbricata is a medicinal plant, native to mountainous regions of Asia, parts of Europe, and the Arctic. Traditionally it is recommended to help combat fatigue and restore energy. It exhibits anti-stress, anti-cancer, and immunostimulatory activities. However, the effect of Rhodiola on immunological responses largely remains unknown. In this study, we have investigated the effect of aqueous extract of R. imbricata rhizome (RAE), on Toll-like receptor-4 (TLR-4) and intracellular granzyme-B expression in mouse splenocytes. Furthermore, TH1/TH2 cytokine profile was analyzed in RAE-treated human peripheral blood mononuclear cells (PBMCs) using multiplex flowcytomix kit. Our findings suggest that RAE induces TLR-4 expression and intracellular granzyme-B in treated splenocytes while RAE stimulated IL-1beta, IL-6, and TNF-alpha in human PBMCs. The present study suggests that RAE stimulates the innate immune pathway and has potent immunostimulatory activity, which can be used in modulating the immune system of immunocompromised individuals.


International Immunopharmacology | 2005

Anti-inflammatory activity of Seabuckthorn (Hippophae rhamnoides) leaves

Lilly Ganju; Y.S. Padwad; Richa Singh; Dev Karan; Sudipta Chanda; Mohinder Kumar Chopra; Parul Bhatnagar; Ravi Kashyap; Ramesh Chandra Sawhney


International Immunopharmacology | 2006

Effect of leaf extract of Seabuckthorn on lipopolysaccharide induced inflammatory response in murine macrophages.

Y.S. Padwad; Lilly Ganju; Monika Jain; Sudipta Chanda; Dev Karan; P.K. Banerjee; R. C. Sawhney


International Immunopharmacology | 2005

Anti-inflammatory activity of Seabuckthorn () leaves

Lilly Ganju; Y.S. Padwad; Raj Kumar Singh; Dev Karan; Sudipta Chanda; M. K. Chopra; Parul Bhatnagar; Ravi Kashyap; R. C. Sawhney


Indian Journal of Experimental Biology | 1999

Immunomodulatory effect of laser on whole body exposure

Lilly Ganju; Salhan A; Dev Karan; Sudipta Chanda; Srivastava Kk

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Lilly Ganju

Defence Institute of Physiology and Allied Sciences

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Sudipta Chanda

Defence Institute of Physiology and Allied Sciences

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R. C. Sawhney

Defence Institute of Physiology and Allied Sciences

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Y.S. Padwad

Defence Institute of Physiology and Allied Sciences

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Monika Jain

Defence Institute of Physiology and Allied Sciences

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K.P. Mishra

Defence Institute of Physiology and Allied Sciences

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K.K. Srivastava

Defence Institute of Physiology and Allied Sciences

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Kshipra Mishra

Defence Institute of Physiology and Allied Sciences

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Ravi Kashyap

International Atomic Energy Agency

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