17 results on '"Sarkar, Riya"'
Search Results
2. Immunomodulation of Macrophages in Diabetic Wound Individuals by Structurally Diverse Bioactive Phytochemicals.
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Adhikary, Krishnendu, Sarkar, Riya, Maity, Sriparna, Sadhukhan, Ishani, Ganguly, Krishnendu, Barman, Saurav, Maiti, Rajkumar, Chakraborty, Sanjoy, Chakraborty, Tandra R., Bagchi, Debasis, and Banerjee, Pradipta
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KILLER cells , *NITRIC-oxide synthases , *CHRONIC wounds & injuries , *PHENOLS , *IMMUNOREGULATION , *WOUND healing - Abstract
Diabetes-related ulcers and slow-healing wounds pose a significant health risk to individuals due to their uncertain causes. Mortality rates for diabetes foot ulcers (DFUs) range from 10% after 16 months to 24% after five years. The use of bioactive phytochemicals can play a key role in healing wounds in a predictable time. Recent literature has demonstrated that various natural substances, including flavonoids, saponins, phenolic compounds, and polysaccharides, play key roles at different stages of the wound-healing process through diverse mechanisms. These studies have categorized the compounds according to their characteristics, bioactivities, and modes of action. In this study, we evaluated the role of natural compounds derived from plant sources that have been shown to play a crucial role in immunomodulation. Macrophages are closely involved in immunomodulation within the wound microenvironment and are key players in efferocytosis, inflammation resolution, and tissue regeneration, all of which contribute to successful wound healing. Phytochemicals and their derivatives have shown capabilities in immune regulation, including macrophage migration, nitric oxide synthase inhibition, lymphocyte and T-cell stimulation, cytokine activation, natural killer cell enhancement, and the regulation of NF-κβ, TNF-α, and apoptosis. In this review, we have studied the role of phytochemicals in immunomodulation for the resolution of diabetic wound inflammation. [ABSTRACT FROM AUTHOR]
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- 2024
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3. The underlying causes, treatment options of gut microbiota and food habits in type 2 diabetes mellitus: a narrative review.
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Adhikary, Krishnendu, Sarkar, Riya, Maity, Sriparna, Banerjee, Ipsita, Chatterjee, Prity, Bhattacharya, Koushik, Ahuja, Deepika, Sinha, Nirmalya Kumar, and Maiti, Rajkumar
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CARRIER proteins ,GUT microbiome ,DIABETIC neuropathies ,INSULIN resistance ,HYPERGLYCEMIA ,MEDLINE ,TYPE 2 diabetes ,FOOD habits ,ONLINE information services - Abstract
Type 2 diabetes mellitus is a long-lasting endocrine disorder characterized by persistent hyperglycaemia, which is often triggered by an entire or relative inadequacy of insulin production or insulin resistance. As a result of resistance to insulin (IR) and an overall lack of insulin in the body, type 2 diabetes mellitus (T2DM) is a metabolic illness that is characterized by hyperglycaemia. Notably, the occurrence of vascular complications of diabetes and the advancement of IR in T2DM are accompanied by dysbiosis of the gut microbiota. Due to the difficulties in managing the disease and the dangers of multiple accompanying complications, diabetes is a chronic, progressive immune-mediated condition that plays a significant clinical and health burden on patients. The frequency and incidence of diabetes among young people have been rising worldwide. The relationship between the gut microbiota composition and the physio-pathological characteristics of T2DM proposes a novel way to monitor the condition and enhance the effectiveness of therapies. Our knowledge of the microbiota of the gut and how it affects health and illness has changed over the last 20 years. Species of the genus Eubacterium, which make up a significant portion of the core animal gut microbiome, are some of the recently discovered 'generation' of possibly helpful bacteria. In this article, we have focused on pathogenesis and therapeutic approaches towards T2DM, with a special reference to gut bacteria from ancient times to the present day. [ABSTRACT FROM AUTHOR]
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- 2024
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4. Chapter 17 - An overview on pathophysiology and therapeutic approaches of Alzheimer's disease and Parkinson's disease
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Adhikary, Krishnendu, Sarkar, Riya, Chowdhury, Sumana Roy, and Banerjee, Pradipta
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- 2024
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5. Chapter 53 - Prion diseases: A rare group of neurodegenerative disorders
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Banerjee, Pradipta, Adhikary, Krishnendu, Sarkar, Riya, Chakraborty, Shrabastee, and Jana, Sasmita
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- 2023
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6. Chapter 9 - Digestion and gut microbiome
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Banerjee, Pradipta, Adhikary, Krishnendu, Chatterjee, Aritra, Sarkar, Riya, Bagchi, Debasis, Ghosh, Nandini, and Das, Amitava
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- 2022
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7. Vancomycin and Linezolid-Resistant Enterococcus Isolates from a Tertiary Care Center in India.
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Sengupta, Mallika, Sarkar, Riya, Sarkar, Soma, Sengupta, Manideepa, Ghosh, Sougata, and Banerjee, Parthajit
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ENTEROCOCCUS , *DISC diffusion tests (Microbiology) , *ENTEROCOCCUS faecalis , *TERTIARY care , *MICROBIAL sensitivity tests , *VANCOMYCIN , *ENTEROCOCCUS faecium - Abstract
Introduction: There is increasing development of antibiotic resistance among the Enterococcus species. Objectives: This study was performed to determine prevalence and characterize the vancomycin-resistant and linezolid-resistant enterococcus isolates from a tertiary care center. Moreover, the antimicrobial susceptibility pattern of these isolates was also determined. Materials and Methods: A prospective study was performed in Medical College, Kolkata, India, over a period of two years (from January 2018 to December 2019). After obtaining clearance from the Institutional Ethics Committee, Enterococcus isolates from various samples were included in the present investigation. In addition to the various conventional biochemical tests, the VITEK 2 Compact system was used to identify the Enterococcus species. The isolates were tested for antimicrobial susceptibility to different antibiotics using the Kirby–Bauer disk diffusion method and VITEK 2 Compact to determine the minimum inhibitory concentration (MIC). The Clinical and Laboratory Standards Institute (CLSI) 2017 guidelines were used to interpret susceptibility. Multiplex PCR was performed for genetic characterization of the vancomycin-resistant Enterococcus isolates and sequencing was performed for characterization of the linezolid-resistant Enterococcus isolates. Results: During the period of two years, 371 isolates of Enterococcus spp. were obtained from 4934 clinical isolates showing a prevalence of 7.52%. Among these isolates, 239 (64.42%) were Enterococcus faecalis, 114 (30.72%) Enterococcus faecium, and others were Enterococcus durans, Enterococcus casseliflavus, Enterococcus gallinarum, and Enterococcus avium. Among these, 24 (6.47%) were VRE (Vancomycin-Resistant Enterococcus) of which 18 isolates were Van A type and six isolates of Enterococcus casseliflavus and Enterococcus gallinarum were resistant VanC type. There were two linezolid-resistant Enterococcus, and they were found to have the G2576T mutation. Among the 371 isolates, 252 (67.92%) were multi-drug resistant. Conclusion: This study found an increasing prevalence of vancomycin-resistant Enterococcus isolates. There is also an alarming prevalence of multidrug resistance among these isolates. [ABSTRACT FROM AUTHOR]
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- 2023
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8. List of contributors
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Achur, Rajeshwar, Adhikary, Krishnendu, Ahire, Eknath D., Akhila, A., Alekhya, Kella, Anousakis, Ch., Ansar, Waliza, Aranha, Ivan, Aravind, Vulli, Arora, Naina, Badgaiyan, Rajendra D., Bagchi, Debasis, Bahekar, Triveni Nilkanth, Balekundri, Amruta, Banerjee, Priyanka, Banerjee, Ritam, Banerjee, Pradipta, Banik, Samudra P., Bansal, Suraj, Baral, Tejaswini, Barh, Debmayla, Baron, David, Batabyal, Nandita, Benson, Ruby, Bhattacharya, Subhrajit, Bhattacharyya, Jhimli, Biswas, Ayan, Biswas, Pallabi, Blanco, Tracey, Blum, Kenneth, Bowirrat, Abdalla, Braverman, Eric R., Chatterjee, Ananya, Chaudhry, Anubha, Chaurasia, Rameshwar Nath, Chowdhury, Sumana Roy, Dakshayini, P.N., Damarasingu, Prasanth, Darshan, J.C., Das, Siddhartha, Das, Arpita, Dasari, Rajasekhar, De, Shaoli, Debnath, Anirban, Dennen, Catherine, Dharmamoorthy, G., Dhavale, Raju K., Dhingra, Sameer, Downs, B. William, Ejaz, Laila, Ejaz, Haris, Elman, Igor, Evangelou, E., Favas, T.T., Garg, Ravindra K., Giordano, John, Gogoi, Maya, Gold, Mark S., Gupta, Munesh Kumar, Gupta, Ashim, Gupta, Abhishek Amod, Han, David, Hanumegowda, Sujatha M., Hati, Subrota, Helan, K.P., Hemachudha, Pasin, Hemachudha, Thiravat, Hossain, Ashfaque, Hostert, Alyssa, Iorio, E.L., Jain, Pushpendra Kumar, Jana, Sudipta, Jawed, Junaid Jibran, Johnson, Aieshel Serafin, Kachave, Ramanlal N., Karati, Dipanjan, Keceli, T.M., Keservani, Raj K., Kesharwani, Rajesh K., Kesharwani, Anuradha, Keshri, Anand Kumar, Khalsa, Jag, Khona, Dolly K., Kiritsakis, Apostolos, Krishnamani, Madhu, Kumar, Anand, Kumar, Podilapu Manoj, Kumar, Neeraj, Kumar, Shivam, Kumar, Nitesh, Kumari, Reena, Kurian, Shilia Jacob, Lall, Neha, Llanos, Luis Gomez, Mahajan, Sunil K., Majumder, Rajib, Makwana, Mitali, Malhotra, Hardeep Singh, Malhotra, Kiran Preet, Mandal, Supriya, McLaughlin, Thomas, Meenakshi, Sarasa, Mehra, Parul, Mendes, Odete, Metkus, Jarred D., Mitra, Mousumi, Mitra, Sudeep, Mohan, Aishvaryaa, Muili, Fatima, Mukherjee, Swarupananda, Mukherjee, Priyanka, Murti, Krishna, Nandi, Dilip Kumar, Narapaka, Pavan Kumar, Njie Mbye, Ya Fatou, Oh, Angela, Ohia, Sunny E., Okolie, Anthonia, Opere, Catherine A., Paliwal, Vimal Kumar, Panda, Satyajit, Parihar, Vipan Kumar, Patil, Dhananjay M., Patil, Sharangouda J., Pattanayak, Sudeepta, Prabhu, Vikas Vittal, Prasad, P. Dharani, Prasad, Amit, Preethi, Pakala, Premalatha, S.J., Raina, Hansika Sanjay, Ramírez, Yael Quiles, Rawat, Suraj Singh, Renuka Jyothi, S., Robinson, Conrad, Roy, Uddappanda Bopaiah, Rupreo, Vibeizonuo, S., Theertha, S.S., Kiron, Saha, Rudra P., Saifeddine, Mohamad, Saini, Ankit Kumar, Samanta, Saptadip, Sannaningaiah, Devaraja, Sanyal, Saptarshi, Saranya, K., Sarkar, Riya, Sen, Amartya, Sengar, Pratishtha, Shahidi, F., Sharma, Swati, Shelke, Akshay, Sheth, Meet, Shibu, Shalmy M., Shivaprasad, H.N., Shukla, Kuldeep, Simpatico, Thomas A., Singh, Abhilasha, Singh, Anshul, Singh, Varun Kumar, Singh, Abhishek Kumar, Singh, Manoj Kumar, Singh, Meghna, Soman, Sauparnika, Sonal Sekhar, M., Sonawane, Deepak D., Sonawane, Vijayraj N., Soni, Gaurav, Sravani, T., Srivastava, Nimish, Srivastava, Chhitij, Surana, Khemchand R., Tejan, Nidhi, Thanos, Panayotis K., Tom, Annmaria, Tsitsipas, Ch., Udaya Kumar, V., Uniyal, Ravi, Urs, Vijeth L., Veeranna, S., Venkatappa, Manjula M., Ward, D. Isum, Wozniak, Lucyna A., Yadav, Latika, and Manasa, Goudicherla
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- 2024
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9. Antiapoptotic and antioxidative efficacy of rhizomes of Curcuma amada on the management of diabetes‐induced male infertility in albino rat: An effective fraction selection study.
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Sarkar, Riya, Mitra, Dipanwita, Ghosh, Prabal, and Ghosh, Debidas
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MALE infertility , *CURCUMA , *SYNTHETIC drugs , *INFERTILITY , *STREPTOZOTOCIN , *ETHYL acetate , *MEDICINAL plants - Abstract
Men with diabetes have negative effects on reproduction that causes sexual dysfunction. Medicinal plants are non‐toxic and much safer than synthetic drugs because regular use of synthetic drugs shows long‐term side effects. Curcuma amada (Roxb) is a medicinal plant used in Ayurveda and Unani medicinal systems in India. The goal of this study is to rummage the potential efficiency of the most potent solvent fraction of effective extract of hydro‐methanol 60:40 of C. amada rhizome on male gonadal hypofunction in streptozotocin‐induced diabetic rat. Diabetes‐induced testicular hypofunction was evaluated by glycemic, spermiological, biochemical, genomic, flow cytometric, and histology of testicular tissue. The n‐hexane, chloroform, ethyl‐acetate, and n‐butanol solvent fractions of the said extract were administrated for 4 weeks at 10 mg dose/100 g body weight/day. Among all the used fractions, the ethyl‐acetate solvent fraction‐treated group showed maximum recovery in serum insulin (177.42%), sperm count (92.84%), sperm motility (97.15%), and serum testosterone (164.33%). The diabetic rats treated with ethyl‐acetate solvent fraction also exhibited the maximum resettlement in flow cytometric analysis of sperm viability (55.84%) and sperm mitochondrial integrity (149.79%), gene expression patterns of key markers for androgenesis (Δ5, 3β‐HSD 87.50%, and 17β‐HSD 74.66%) and apoptosis (Bax 44.63%, Bcl‐2 54.03%, and Caspase‐3 35.77%) along with testicular histology. The ethyl‐acetate fraction contains alkaloids, flavonoids, and polyphenols where all of these components are not present in other fractions, may be the most effective cause for the recovery of diabetes‐linked oxidative stress‐mediated testicular hypofunctions. Practical applications: Nowadays worldwide, the use of synthetic drugs are reduced due to their toxic effect. At present, synthetic drugs are replaced by several herbal drugs, the natural source of medicine which has many therapeutic values. C. amada has strong antioxidant activity due to the presence of bio‐active compound(s) that can able to manage streptozotocin‐induced diabetes linked to oxidative damage of male gonadal organs. Therefore, these bio‐active compound(s)‐containing said medicinal plant may use as a good source of antioxidative food in the food industry as nutraceuticals and in pharmaceutical industries for the development of the herbal drug to manage diabetes‐linked male gonadal hypofunctions. At present, WHO also gives emphasis for developing one drug‐multi‐disease therapy. From such a viewpoint, this active fraction‐containing phytomolecules may have corrective efficacy against diabetes as well as oxidative stress‐linked testicular complications. [ABSTRACT FROM AUTHOR]
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- 2022
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10. Contributors
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Adhikary, Krishnendu, Affinati, Brenda, Ahmed, Amany M., Al Saadi, Mahmoud, Alkutbi, Alisar, Al-Shar’i, Nizar A., Ansar, Waliza, Arora, Prachi, Bagchi, Debasis, Bagchi, Manashi, Baheti, Akshay M., Baliga, Vineet, Ballambattu, Vishnu Bhat, Banerjee, Pradipta, Banerjee, Priyanka, Banik, Samudra Prosad, Baral, Tejaswini, Bardaweel, Sanaa K., Barros, Nicolas, Basak, Pijush, Becken, III, Bradford A., Bhagyalakshmi, M., Bhattacharya, Joyeeta, Bhattacharya, Mohini, Bhattacharyya, Jhimli, Bhattacharyya, Maitree, Bhattacherjee, Ashmita, Bhavya, Karanam Sai, Bhutia, Rinchen Doma, Birudala, Geetha, Birudala, Ramadevi, Biswas, Ayan, Biswas, Nabendu, Biswas, Sanchita, Biswas, Shaoli, Borah, Pobitra, Bose, Sayantan, Bula Rudas, Fernando J., Chakrabarty, Subhendu, Chakraborti, Modhurima, Chakraborty, Atreyee, Chakraborty, Sanjoy, Chakraborty, Shrabastee, Chakraborty, Sudipta, Chandrasekar, S.B., Chatterjee, Archana, Chatterjee, Aritra, Chatterjee, Gourab, Chatterjee, Rituparna, Chatterjee, Tanima, Chaurasia, Rameshwar Nath, Chen, Bo-Kai, Chettri, Ashna, Chiu, Hui-Fang, Choudhury, Antara, Chowdhury, Sailee, Chowdhury, Sougata Roy, Collins, Courtney, Colomb, Elaine, Cuevas-Galindo, M. Emilio, Das, Amitava, Das, Amlan, Das, Arpita, Das, Dibya, Das, Mousumi, Deb, Pran Kishore, Deb, Sujoy, Debnath, Anirban, Deka, Satyendra, Delair, Shirley F., Delia, Alyssa, Desai, Karishma, Devaraja, S., Dey, Priyankar, Dolma, Karma Gurmey, Downs, Bernard William, Downs, Jaclyn M., Eguiguren, Lourdes, El Masry, Mohamed S., Estevez-Fregoso, Elizabeth, Farfán-García, Eunice D., Ferdous, Zannatul, Ganesan, Ramakrishnan, García-Coronel, Itzel H., García-Machorro, Jazmín, George, Roseline, Ghosh, Nandini, Ghosh, Rituparna, Ghosh, Santanu, Goswami, Arunava, Gourishetti, Karthik, Guith, Tanner, Gurugubelli, Krishna Rao, Hassan, Dania, Hazarika, Sangeeta, Hegde, Vijay, Hossain, Ashfaque, Hossain, Sheikh Shah, Hurst, Amanda L., Jalilvand, Anahita, Jana, Sasmita, Jawed, Junaid Jibran, Jorge, Miguel, Kacar, Sedat, Kansal, Vikash, Kar, Nabanita, Karim, Muhammad Manjurul, Khandelwal, Bidita, Kilic, Ahmet, Koirala, Prakash, Kubal, Chandrashekhar, Kumar, Abhai, Kumar, Umesh, Kumar, V., Kumari, Leena, Kushner, Steve, Lopez, Santiago M.C., Madhu, Maxima, Maitra, Puja, Maji, Himangshu Sekhar, Maji, Sushomasri, Majumder, Rajib, Mandal, Labonya, Mandal, Supriya, McGwire, Bradford S., Mendes, Odete R., Mennuru, Nagendra Babu, Miraj, Sonal Sekhar, Mitra, Sutanuka, Moludi, Jalal, Mukherjee, Sandipan, Munisamy, Murali, Murti, Krishna, NandyMazumdar, Monali, Nateqi, Masoud, Neemann, Kari A., Nguyen, Andrew, Ovung, Aben, Pal, Kunal, Pawar, Anil T., Potty, Prakash Narayanan Vasudevan, Rana, Megha, Rao, Mahadev, Ray, Sayantan, Ray Dutta, Jayati, Rokop, Zachary P., Roy, Sashwati, Rubio-Velazquez, Brenda A., Saha, Abinit, Saha, Rudra P., Saha, Tiyas, Samanta, Saptadip, Sanyal, Saptarshi, Sarkar, Dipayan, Sarkar, Dipika, Sarkar, Riya, Sato, Alice I., Satoskar, Abhay R., Sen, Abhishek Kumar, Sen, Chandan K., Sengupta, Pracheta, Shah, Aditi, Sharma, Dikshya, Shinu, Pottathil, Shivaprasad, H.N., Shrikar Reddy, B., Sil, Moumita, Singh, Abhilasha, Singh, Kanhaiya, Singh, Manoj Kumar, Singh, Smita, Singh, Varun Kumar, Sirisha Mulukuri, N.V.L., Smith, Jessica, Soriano-Ursúa, Marvin A., Srinivas, Shruthi, Sultana, Shahnaz, Talukdar, Arindam, Tata, Pranathi, Thomas, Levin, Trujillo-Ferrara, Jose G., Uddin, Md. Hafiz, Varma, Muralidhar, Varman, Meera, Venugopala, Katharigatta N., Verma, Priyanka, Vishwanath, Shashidhar, Vyas, Navya, Wang, Chin-Kun, Wisler, Jon, and Yadav, Nilesh
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- 2023
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11. Contributors
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Adhikary, Krishnendu, Agarwal, Amit, Akil Hossain, Md, Fadhlizil Fasihi Mohd Aluwi, Mohd, Ang, Lin, Anusha, Siddaraju, Armine, Jess, Babaria, Radhika, Bagchi, Debasis, Bagchi, Manashi, Banerjee, Bhaskar, Banerjee, Pradipta, Banik, Samudra Prosad, Baral, Tejaswini, Basu, Priyadarshi, Bethapudi, Bharathi, Bhatttacharyya, Jhimli, Biswas, Nabendu, Bukowiecka-Matusiak, Malgorzata, Burzynska-Pedziwiatr, Izabela, Bush, Leah, Chakraborty, Sanjoy, Chatterjee, Ankita, Chatterjee, Aritra, Chatterjee, Sabyasachi, Chawla, Smriti, Das, Amitava, Das, Dolan, Das, Sujit, Devaraja, S., Downs, Bernard W., Downs, Jaclyn, Ghosh, Nandini, Golovinskaia, Oksana, Handa, Osamu, Hati, Subrota, Hip Kam, Annaelle, Jalan, Komal, Kathi, Pradeep Reddy, Kim, Myung-Sunny, Kopeć, Aneta, Kukkupuni, Subrahmanya Kumar, Kurian, Shilia Jacob, Kushner, Steve, Lee, Hye Won, Lee, Myeong Soo, Maji, Himangshu Sekhar, Mandal, Labonya, Mavani, A., Moyeenul Huq, A.K.M., Muili, Fatima, Mundkinajeddu, Deepak, Murugan, Sasi Kumar, Nair, Sreejayan, Naito, Yuji, Neergheen, Vidushi S., Negi, Pradeep Singh, Ngele, Kalu, Nithyanantham, Muruganantham, Njie-Mbye, Ya Fatou, Ohia, Sunny E., Okolie, Anthonia, Opere, Catherine A., Preuss, Harry G., Rao, Mahadev, Ray, Moumita, Rout, Akanksha, Rumman, Marufa, Saji, Hephzibah, Samanta, Saptadip, Sarkar, Riya, Sato, Kenji, Sehgal, Shalini, Sekhar M, Sonal, Sharath kumar, M.N., Shirako, Saki, Singh, Abhilasha, Singh, Vineet Kumar, Smith, Derek, Song, Eunhye, Sowmyashree, G., Takagi, Tomohisa, Uddin, Md Hafiz, Vishnuprasad, Chethala N., Wada, Sayori, Wang, Chin-Kun, Wozniak, Lucyna A., Yoshinari, Orie, and Zawistowski, Jerzy
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- 2022
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12. Antidiabetic and antioxidative properties of the hydro-methanolic extract (60:40) of rhizomes of Curcuma amada roxb. (Zingiberaceae) in streptozotocin-induced diabetic male albino rat: a dose-dependent study through biochemical and genomic approaches.
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Mitra, Dipanwita, Sarkar, Riya, and Ghosh, Debidas
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AMINOGLYCOSIDES ,AMINOTRANSFERASES ,ANIMAL experimentation ,ASPARTATE aminotransferase ,BLOOD sugar ,BODY weight ,CARBOHYDRATE metabolism ,CARBOXYLIC acids ,CELL physiology ,CONVALESCENCE ,DIABETES ,FASTING ,GENE expression ,INSULIN ,ISLANDS of Langerhans ,LIVER ,METHANOL ,ONCOGENES ,RATS ,PLANT roots ,TRADITIONAL medicine ,PLANT extracts ,GENOMICS ,OXIDATIVE stress ,EXCITATORY amino acid agents - Abstract
Background: Curcuma amada is the most popular traditional medicine in India for the treatment of diabetes. The present study aimed to focus the antidiabetic and antioxidative activity of C. amada through the analysis of biochemical and genomic levels in a dose-dependent manner in streptozotocin-induced male adult rat. Method: Streptozotocin-induced diabetic rats were administered orally with hydro-methanolic extract of C. amada at the dose of 10, 20, 40 and 80 mg/100 g body weight of rats for 28 days. The antidiabetic and antioxidative efficacy of the extract on glycemic, enzymatic, genomic and histological sensors along with toxicity study was investigated. Results: The result showed a significant antidiabetic and antioxidative effect of the extract at dose-dependent manner. The significant recovery of fasting blood glucose level, serum insulin, activity of carbohydrate metabolic enzymes and antioxidative enzymes in extract-treated diabetic group as compared to untreated diabetic group were noted. After the extract treatment, the size of pancreatic islet and cell population densities were significantly increased. Activities of glutamate oxaloacetate transaminase and glutamate pyruvate transaminase in liver were significantly recovered along with the correction of Bax and Bcl-2 gene expression in hepatic tissue after the extract treatment in diabetic rats in respect to untreated diabetic group. Out of all the doses, the significant effects were noted at the dose of 20 mg/100 g body weight which has been considered as threshold dose in the concern. Conclusion: It may be concluded that the significant and corrective effect in most of the sensors was noted at the minimum dose of 20 mg/100 g body weight of hydro-methanolic extract of C. amada without producing any toxicity. [ABSTRACT FROM AUTHOR]
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- 2019
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13. Biofilm Producing Enterococcus Isolates from Vaginal Microbiota.
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Sengupta, Mallika, Sarkar, Soma, SenGupta, Manideepa, Ghosh, Sougata, Sarkar, Riya, and Banerjee, Parthajit
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ENTEROCOCCUS ,MICROBIAL sensitivity tests ,BIOFILMS ,ENTEROCOCCUS faecalis ,GRAM'S stain ,ENTEROCOCCUS faecium - Abstract
Background: Enterococcus is an important cause of infection in the hospital as well as in the community. Methods: A prospective study was done in Medical College, Kolkata for a period of 2 years (from January 2018 to December 2019). After obtaining clearance from the Institutional Ethics Committee, Enterococcus isolates from cases of vaginitis were included in the study. Identification of Enterococcus species was done by Gram stain and conventional biochemical tests along with automated identification by VITEK 2 Compact. These isolates were tested for antimicrobial susceptibility to different antibiotics by Kirby Bauer disc diffusion method and minimum inhibitory concentration (MIC) by VITEK 2 Compact. Interpretation of susceptibility was done according to the Clinical and Laboratory Standards Institute (CLSI) 2017 guidelines. Biofilm detection for Enterococcus species was done. Results: During the period of 2 years, 39 isolates of Enterococcus spp. were obtained from vaginitis cases. Among these, 27 were Enterococcus faecalis and 12 Enterococcus faecium. All isolates were highly susceptible to vancomycin, teicoplanin, and linezolid. Biofilm was detected in eight isolates of which five were strong biofilm producer and three moderate biofilm producers. Conclusion: Biofilm production is an important virulence factor in Enterococcus isolates from vaginitis. [ABSTRACT FROM AUTHOR]
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- 2021
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14. Correction of diabetes‐induced testicular dysfunction by a hydro‐methanol (60:40) extract of Curcuma amada rhizomes: A dose‐dependent study.
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Sarkar, Riya, Ghosh, Prabal, Tripathy, Adrija, and Ghosh, Debidas
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CURCUMA , *SPERM motility , *GENE expression , *GENITALIA , *TESTIS injuries , *STREPTOZOTOCIN - Abstract
Diabetes affects the reproductive system. This study was conducted to find out the potent dose of the hydro‐methanol 60:40 extract of Curcuma amada rhizomes for the management of diabetes‐induced testicular dysfunction in albino rats. The extract was administered at the doses of 10, 20, 40, and 80 mg/100 g body weight/day for 28 days. Oxidative stresses, reproductive parameters, histological, and gene expressions of the testicular tissue were assessed. Out of the doses used, the 20‐mg dose showed maximum recovery as the minimum dose (e.g., sperm motility 112.03%, testicular cholesterol 34.86%, Bax gene expression 49.77%), whereas 40‐ and 80‐mg doses did not vary statistically with each other (e.g., sperm motility 95.37% and 89.19%, testicular cholesterol 30.42% and 28.41%, Bax gene expression 47.33% and 46.18%, respectively) as well as with the 20‐mg dose. It may be concluded that the 20‐mg dose is the threshold dose for this purpose. Practical applications: The hydro‐methanol 60:40 extract of rhizomes of Curcuma amada has a strong antioxidant property that can manage diabetes‐induced oxidative injuries in testes which may raise a hope to the pharmaceutical industries to develop a herbal drug for diabetes‐linked testicular hypofunction management. [ABSTRACT FROM AUTHOR]
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- 2019
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15. Japanese encephalitis virus hijacks ER-associated degradation regulators for its replication.
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Sarkar R, Chhabra S, Tanwar M, Agarwal N, and Kalia M
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- Humans, HeLa Cells, Host-Pathogen Interactions, Endoplasmic Reticulum metabolism, Endoplasmic Reticulum virology, Proteins metabolism, Proteins genetics, Antigens, Differentiation, Virus Replication, Encephalitis Virus, Japanese physiology, Encephalitis Virus, Japanese genetics, Endoplasmic Reticulum-Associated Degradation, Ubiquitin-Protein Ligases metabolism, Ubiquitin-Protein Ligases genetics, Membrane Proteins metabolism, Membrane Proteins genetics
- Abstract
Flaviviruses target their replication on membranous structures derived from the ER, where both viral and host proteins play crucial structural and functional roles. Here, we have characterized the involvement of the ER-associated degradation (ERAD) pathway core E3 ligase complex (SEL1L-HRD1) regulator proteins in the replication of Japanese encephalitis virus (JEV). Through high-resolution immunofluorescence imaging of JEV-infected HeLa cells, we observe that the virus replication complexes marked by NS1 strongly colocalize with the ERAD adapter SEL1L, lectin OS9, ER-membrane shuttle factor HERPUD1, E3 ubiquitin ligase HRD1 and rhomboid superfamily member DERLIN1. NS5 positive structures also show strong overlap with SEL1L. While these effectors show significant transcriptional upregulation, their protein levels remain largely stable in infected cells. siRNA mediated depletion of OS9, SEL1L, HERPUD1 and HRD1 significantly inhibit viral RNA replication and titres, with SEL1L depletion showing the maximum attenuation of replication. By performing protein translation arrest experiments, we show that SEL1L, and OS9 are stabilised upon JEV infection. Overall results from this study suggest that these ERAD effector proteins are crucial host-factors for JEV replication.
- Published
- 2024
- Full Text
- View/download PDF
16. Japanese encephalitis virus capsid protein interacts with non-lipidated MAP1LC3 on replication membranes and lipid droplets.
- Author
-
Sarkar R, Sharma KB, Kumari A, Asthana S, and Kalia M
- Subjects
- Amino Acid Sequence, Animals, Capsid chemistry, Capsid metabolism, Capsid Proteins chemistry, Cell Line, Encephalitis Virus, Japanese metabolism, Host-Pathogen Interactions, Humans, Mice, Molecular Docking Simulation, Protein Interaction Domains and Motifs, Virus Replication, Capsid Proteins metabolism, Encephalitis Virus, Japanese physiology, Lipid Droplets metabolism, Microtubule-Associated Proteins metabolism, Viral Replication Compartments metabolism
- Abstract
Microtubule-associated protein 1 light chain 3 (MAP1LC3) is a protein with a well-defined function in autophagy, but still incompletely understood roles in several other autophagy-independent processess. Studies have shown MAP1LC3 is a host-dependency factor for the replication of several viruses. Japanese encephalitis virus (JEV), a neurotropic flavivirus, replicates on ER-derived membranes that are marked by autophagosome-negative non-lipidated MAP1LC3 (LC3-I). Depletion of LC3 exerts a profound inhibition on virus replication and egress. Here, we further characterize the role of LC3 in JEV replication, and through immunofluorescence and immunoprecipitation show that LC3-I interacts with the virus capsid protein in infected cells. This association was observed on capsid localized to both the replication complex and lipid droplets (LDs). JEV infection decreased the number of LDs per cell indicating a link between lipid metabolism and virus replication. This capsid-LC3 interaction was independent of the autophagy adaptor protein p62/Sequestosome 1 (SQSTM1). Further, no association of capsid was seen with the Gamma-aminobutyric acid receptor-associated protein family, suggesting that this interaction was specific for LC3. High-resolution protein-protein docking studies identified a putative LC3-interacting region in capsid,
56 FTAL59, and other key residues that could mediate a direct interaction between the two proteins.- Published
- 2021
- Full Text
- View/download PDF
17. Seroprevalence and Co-infection of Hepatitis B and Hepatitis C among Patients in a Tertiary Care Hospital in Eastern India.
- Author
-
Rahaman J, Sengupta M, Barik G, Sarkar S, Sarkar R, and Sengupta M
- Subjects
- Humans, India epidemiology, Male, Seroepidemiologic Studies, Tertiary Care Centers, Coinfection, HIV Infections epidemiology, Hepatitis B epidemiology, Hepatitis C epidemiology
- Abstract
Introduction: Hepatitis B (HBV) and Hepatitis C (HCV) are two common viral infections causing cirrhosis., Aim: The aim of this study was to find the seroprevalence of HBV and HCV along with occurrence of co-infection of HBV and HCV in patients attending a tertiary care hospital., Materials and Methods: The study was done for a period of one year (January to December 2016) in the Department of Microbiology, Medical College, Kolkata. After obtaining ethical clearance and informed consent from the patients, serum samples were collected from all patients referred to Department of Microbiology for antibody to HCV and Hepatitis B surface antigen (HBsAg) screening. ELISA was performed for anti HCV antibody and HBsAg. The results and relevant clinical information were noted and analysis was done., Results: A total of 10802 samples were received, of which 316 (2.92 %) were HBsAg positive, 115 (1.06%) were HCV antibody positive and a total of 7 (0.07%) patients were positive both for HBsAg and Anti HCV antibody. There was male preponderance. Anti HCV antibody was more common in age below 10 years and in thalassemia patients. Out of 7 patients positive for both, 5 patients were on regular blood transfusion due to beta thalassemia and 2 patients had history of chronic liver disease., Conclusion: In this study, it was found that there was seroprevalence of 2.92 % of HBsAg, 1.06% of HCV antibody and 0.07% positive both for HBsAg and HCV antibody among the patients of a tertiary care centre in Eastern India., (© Journal of the Association of Physicians of India 2011.)
- Published
- 2019
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