Saptadip Samanta
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Saptadip Samanta has a total of 214 co-authors. Here are the top co-authors by number of shared publications:
- Debasis Bagchi
Department of Biology, College of Arts and Sciences, Adelphi University, Garden City, NY 11530, USA
3 shared publications Debasis Bagchi
Department of Biology, College of Arts and Sciences, Adelphi University, Garden City, USA
2 shared publicationsDilip Kumar Nandi
Department of Physiology, Raja N.L. Khan Women’s College (Autonomous)
2 shared publicationsSomnath Gangopadhyay
Department of Physiology, Occupational Ergonomics Laboratory, University College of Science and Technology, University of Calcutta
2 shared publicationsA. Akhila
1 shared publicationAbdalla Bowirrat
1 shared publication
Latest Publications
- 24 April 2025
- Published by Taylor & Francis in Archives of Physiology and Biochemistry
- Vol. 131 (5) , 728-735
Protective role of butylated hydroxyanisole (BHA) and hydroxytoluene (BHT) against oxidative stress-induced inflammatory response in carbon tetrachloride-induced acute hepatorenal toxicity
Any toxicity initially damages the hepatic system, followed by renal dysfunction. Previously, it was established that carbon tetrachloride (CCl4) intoxication severely damaged hepatocytes. Moreover, CCl4-mediated toxicity significantly impacted immune functions and influenced the inflammatory response, with mitochondrial dysfunction. The present study focused on the levels of inflammatory markers and mitochondrial dysfunction, as well as the protective role of BHA and BHT. In the present study, hepatorenal dysfunction was developed in experimental rats by applying a subcutaneous injection of CCl4 with a dose of 230 mg/kg bwt/rat/day. The level of immune toxicity was determined by measuring C-reactive protein (CRP), IL-6, 12, TNF-α, IL-10, and TGF-β in CCl4 intoxicated group and pretreated BHA and BHT groups. ROS generation and MMP were also measured in hepatic and renal cells using flow cytometric technique. The level of toxicity was determined by a significant increase of CRP (407.29%), IL-6 (525.65%), IL-12 (1026.54%), and TNF-α (1007.33%) in CCl4 intoxicated group, while IL-10 and TGF-β were significantly decreased 84.65% and 66.36%, respectively. CCl4 intoxication caused decreased mitochondrial membrane potential and high levels of intracellular ROS generation. Pretreatment with BHA (0.5 mg/kg/bwt) and BHT (0.8 mg/kg/bwt) significantly (pp<0.05) reduced inflammatory markers in the CCl4-treated group, restored mitochondrial membrane potential and decreased intracellular ROS levels. BHA and BHT treatment could restrict the higher concentration of pro-inflammatory markers by scavenging ROS. Therefore, the study suggested that supplementation of BHA and BHT could be an alternative treatment for preventing hepatorenal dysfunctions.
- 24 April 2025
- Published by Taylor & Francis in Archives of Physiology and Biochemistry
- Vol. 131 (5) , 728-735
Protective role of butylated hydroxyanisole (BHA) and hydroxytoluene (BHT) against oxidative stress-induced inflammatory response in carbon tetrachloride-induced acute hepatorenal toxicity
Any toxicity initially damages the hepatic system, followed by renal dysfunction. Previously, it was established that carbon tetrachloride (CCl4) intoxication severely damaged hepatocytes. Moreover, CCl4-mediated toxicity significantly impacted immune functions and influenced the inflammatory response, with mitochondrial dysfunction. The present study focused on the levels of inflammatory markers and mitochondrial dysfunction, as well as the protective role of BHA and BHT. In the present study, hepatorenal dysfunction was developed in experimental rats by applying a subcutaneous injection of CCl4 with a dose of 230 mg/kg bwt/rat/day. The level of immune toxicity was determined by measuring C-reactive protein (CRP), IL-6, 12, TNF-α, IL-10, and TGF-β in CCl4 intoxicated group and pretreated BHA and BHT groups. ROS generation and MMP were also measured in hepatic and renal cells using flow cytometric technique. The level of toxicity was determined by a significant increase of CRP (407.29%), IL-6 (525.65%), IL-12 (1026.54%), and TNF-α (1007.33%) in CCl4 intoxicated group, while IL-10 and TGF-β were significantly decreased 84.65% and 66.36%, respectively. CCl4 intoxication caused decreased mitochondrial membrane potential and high levels of intracellular ROS generation. Pretreatment with BHA (0.5 mg/kg/bwt) and BHT (0.8 mg/kg/bwt) significantly (pp<0.05) reduced inflammatory markers in the CCl4-treated group, restored mitochondrial membrane potential and decreased intracellular ROS levels. BHA and BHT treatment could restrict the higher concentration of pro-inflammatory markers by scavenging ROS. Therefore, the study suggested that supplementation of BHA and BHT could be an alternative treatment for preventing hepatorenal dysfunctions.
- Open Access
- 1 October 2024
- Published by Taylor & Francis in Psychology Research and Behavior Management
- Vol. ume 17, 3485-3501
A Complex Relationship Among the Circadian Rhythm, Reward Circuit and Substance Use Disorder (SUD)
Dove Press is a member of the Open Access Initiative, specializing in peer reviewed Medical Journals. View articlesor submit your research for publishing
- 1 October 2024
- Published by Taylor & Francis in Psychology Research and Behavior Management
- Vol. ume 17, 3485-3501
Open AccessA Complex Relationship Among the Circadian Rhythm, Reward Circuit and Substance Use Disorder (SUD)
Dove Press is a member of the Open Access Initiative, specializing in peer reviewed Medical Journals. View articlesor submit your research for publishing
- Open Access
- 31 August 2024
- Published by ACS Publisher in The Indian Journal of Animal Reproduction
- Vol. 45 (2) , 22-35
Quality and Biochemical Characteristics of Frozen Semen of Purebred and Crossbred Bulls
In the present study, frozen semen straw were collected from the bull semen bank and performed routine semen analysis. We also studied different biochemical parameters of seminal fluid, including ROS generation and DNA fragmentation. Average viability and motility of sperm showed within 77% and 27%, respectively, which is not satisfactory. Biochemical constituents like glucose, fructose, total protein, cholesterol, and others varied among the different breeds, and there was no superiority among the breeds. The results of different electrolyte concentrations were closely associated among the different breeds that protected the sperm from osmotic lysis. Aspartate transaminase, alanine transaminase, alkaline phosphatase, and acid phosphatase activity were mostly better in exotic and crossbred breeds than in pure indigenous breeds. Antioxidant profile and oxidative stress (OS) were also studied. The results indicated that antioxidant enzyme (catalase, GPx) activity and reduced glutathione content were high in the crossbred variety. However, lipid peroxidation rate was high in the Gir breed. Flowcytometry study revealed that the ROS generation level was very high, and the rate of DNA fragmentation was around 50%, which indicated the loss of 50% of sperm due to ROS. In conclusion, it could be said that cryopreservation decreases sperm viability, motility, and increases ROS that is detrimental to sperm survival.
- 31 August 2024
- Published by ACS Publisher in The Indian Journal of Animal Reproduction
- Vol. 45 (2) , 22-35
Open AccessQuality and Biochemical Characteristics of Frozen Semen of Purebred and Crossbred Bulls
In the present study, frozen semen straw were collected from the bull semen bank and performed routine semen analysis. We also studied different biochemical parameters of seminal fluid, including ROS generation and DNA fragmentation. Average viability and motility of sperm showed within 77% and 27%, respectively, which is not satisfactory. Biochemical constituents like glucose, fructose, total protein, cholesterol, and others varied among the different breeds, and there was no superiority among the breeds. The results of different electrolyte concentrations were closely associated among the different breeds that protected the sperm from osmotic lysis. Aspartate transaminase, alanine transaminase, alkaline phosphatase, and acid phosphatase activity were mostly better in exotic and crossbred breeds than in pure indigenous breeds. Antioxidant profile and oxidative stress (OS) were also studied. The results indicated that antioxidant enzyme (catalase, GPx) activity and reduced glutathione content were high in the crossbred variety. However, lipid peroxidation rate was high in the Gir breed. Flowcytometry study revealed that the ROS generation level was very high, and the rate of DNA fragmentation was around 50%, which indicated the loss of 50% of sperm due to ROS. In conclusion, it could be said that cryopreservation decreases sperm viability, motility, and increases ROS that is detrimental to sperm survival.
- Open Access
- 23 August 2024
- Published by Open Exploration Publishing
- Vol. 3 (4) , 321-351
An intricate relationship between circadian rhythm dysfunction and psychiatric diseases
There is a complex relationship between circadian rhythm dysfunctions and various psychiatric disorders. Circadian (~24 h) rhythms indicate the rhythmic change of different physiological activities in relation to the environmental light-dark cycle. Shift work, light exposure at night, and chronic and acute jet lag affect circadian rhythm that have a negative impact on psychological functions, and behaviors. Additionally, professional stress, mental instability, and social disintegration influence psychiatric disorders. PubMed/MEDLINE, Springer Nature, Science Direct (Elsevier), Wiley Online, ResearchGate, and Google Scholar databases were searched to collect relevant articles. Circadian rhythm disruption causes impaired neurotransmitter release, impaired melatonin and cortisol rhythm, metabolic dysfunctions, neuroinflammation, and neural apoptosis; collectively these factors influence the development of psychiatric disorders. Circadian dysfunction also alters the expression of several clock control genes in the mesolimbic areas that are associated with pathologies of psychiatric disorders. Additionally, chronotherapy and applications of anti-psychotic medicine can improve psychiatric diseases. This review focuses on the effects of circadian clock dysfunction on the vulnerability of psychiatric disorders and the implications of chronotherapy.
- 23 August 2024
- Published by Open Exploration Publishing
- Vol. 3 (4) , 321-351
Open AccessAn intricate relationship between circadian rhythm dysfunction and psychiatric diseases
There is a complex relationship between circadian rhythm dysfunctions and various psychiatric disorders. Circadian (~24 h) rhythms indicate the rhythmic change of different physiological activities in relation to the environmental light-dark cycle. Shift work, light exposure at night, and chronic and acute jet lag affect circadian rhythm that have a negative impact on psychological functions, and behaviors. Additionally, professional stress, mental instability, and social disintegration influence psychiatric disorders. PubMed/MEDLINE, Springer Nature, Science Direct (Elsevier), Wiley Online, ResearchGate, and Google Scholar databases were searched to collect relevant articles. Circadian rhythm disruption causes impaired neurotransmitter release, impaired melatonin and cortisol rhythm, metabolic dysfunctions, neuroinflammation, and neural apoptosis; collectively these factors influence the development of psychiatric disorders. Circadian dysfunction also alters the expression of several clock control genes in the mesolimbic areas that are associated with pathologies of psychiatric disorders. Additionally, chronotherapy and applications of anti-psychotic medicine can improve psychiatric diseases. This review focuses on the effects of circadian clock dysfunction on the vulnerability of psychiatric disorders and the implications of chronotherapy.
- 15 August 2024
- Published by Springer Nature in Journal of Physiology and Biochemistry
- Vol. 80 (4) , 757-774
Physiological and metabolic functions of the β3-adrenergic receptor and an approach to therapeutic achievements
A specific type of beta-adrenergic receptor was discovered in the decade of 1980s and subsequently recognized as a new type of beta-adrenergic receptor, called beta3-adrenoceptor (β3-AR). β3-AR expresses in different tissues, including adipose tissue, gall bladder, stomach, small intestine, cardiac myocytes, urinary bladder, and brain. Structurally, β3-AR is very similar to β1- and β2-AR and belongs to a G-protein coupled receptor that uses cAMP as an intracellular second messenger. Alternatively, it also activates the NO-cGMP cascade. Stimulation of the β3-AR increases lipolysis, fatty acid oxidation, energy expenditure, and insulin action, leading to anti-obesity and anti-diabetic activity. Moreover, β3-AR differentially regulates the myocardial contraction and relaxes the urinary bladder to balance the cardiac activity and delay the micturition reflex, respectively. In recent years, this receptor has served as an attractive target for the treatment of obesity, type 2 diabetes, congestive heart failure, and overactive bladder syndrome. Several β3-AR agonists are in the emerging stage that can exert novel pharmacological benefits in different therapeutic areas. The present review focuses on the structure, signaling, physiological, and metabolic activities of β3-AR. Additionally, therapeutic approaches of β3-AR have also been considered.
- 15 August 2024
- Published by Springer Nature in Journal of Physiology and Biochemistry
- Vol. 80 (4) , 757-774
Physiological and metabolic functions of the β3-adrenergic receptor and an approach to therapeutic achievements
A specific type of beta-adrenergic receptor was discovered in the decade of 1980s and subsequently recognized as a new type of beta-adrenergic receptor, called beta3-adrenoceptor (β3-AR). β3-AR expresses in different tissues, including adipose tissue, gall bladder, stomach, small intestine, cardiac myocytes, urinary bladder, and brain. Structurally, β3-AR is very similar to β1- and β2-AR and belongs to a G-protein coupled receptor that uses cAMP as an intracellular second messenger. Alternatively, it also activates the NO-cGMP cascade. Stimulation of the β3-AR increases lipolysis, fatty acid oxidation, energy expenditure, and insulin action, leading to anti-obesity and anti-diabetic activity. Moreover, β3-AR differentially regulates the myocardial contraction and relaxes the urinary bladder to balance the cardiac activity and delay the micturition reflex, respectively. In recent years, this receptor has served as an attractive target for the treatment of obesity, type 2 diabetes, congestive heart failure, and overactive bladder syndrome. Several β3-AR agonists are in the emerging stage that can exert novel pharmacological benefits in different therapeutic areas. The present review focuses on the structure, signaling, physiological, and metabolic activities of β3-AR. Additionally, therapeutic approaches of β3-AR have also been considered.
- 7 June 2024
- Published by Elsevier
- p. 481-496
Neurodegenerative diseases and circadian rhythm dysfunction: A bidirectional nexus
- 7 June 2024
- Published by Elsevier
- p. 481-496
Neurodegenerative diseases and circadian rhythm dysfunction: A bidirectional nexus
- 7 June 2024
- Published by Elsevier
List of contributors
- Open Access
- 22 March 2024
- Published by Scientific Scholar in South Asian Journal of Health Sciences
- p. 1-6
Impact of the gut–brain axis on neurodegenerative diseases and potential benefits of probiotics
Gut microbiota are an essential community for human health. They produce different bioactive components and short-chain fatty acids for physiological benefits. Intestinal flora elicits an immune response and maintains a balance between inflammatory and anti-inflammatory cytokines during the inflammatory response. The intricate relationship between the activities of gut microbes and brain functions creates the gut–brain axis. Microbial metabolites of the gut reach the brain through blood and lymphatic circulation. The bioactive components from gut microorganisms regulate oxidative stress, cytokine profiles, neuroinflammation, apoptotic reactions and neurodegeneration. Dysbiosis alters the activity of gut microbiota, which causes gastrointestinal disorders, neurodegenerative diseases, metabolic syndrome and cancers. Probiotic bacteria (Lactobacillus spp., Bifidobacterium spp.) have different health promotional effects and exhibit a significant role in immunomodulation. These bacteria display some protective role against various diseases, including neurodegenerative disorders.
- 22 March 2024
- Published by Scientific Scholar in South Asian Journal of Health Sciences
- p. 1-6
Open AccessImpact of the gut–brain axis on neurodegenerative diseases and potential benefits of probiotics
Gut microbiota are an essential community for human health. They produce different bioactive components and short-chain fatty acids for physiological benefits. Intestinal flora elicits an immune response and maintains a balance between inflammatory and anti-inflammatory cytokines during the inflammatory response. The intricate relationship between the activities of gut microbes and brain functions creates the gut–brain axis. Microbial metabolites of the gut reach the brain through blood and lymphatic circulation. The bioactive components from gut microorganisms regulate oxidative stress, cytokine profiles, neuroinflammation, apoptotic reactions and neurodegeneration. Dysbiosis alters the activity of gut microbiota, which causes gastrointestinal disorders, neurodegenerative diseases, metabolic syndrome and cancers. Probiotic bacteria (Lactobacillus spp., Bifidobacterium spp.) have different health promotional effects and exhibit a significant role in immunomodulation. These bacteria display some protective role against various diseases, including neurodegenerative disorders.
- 1 January 2024
- Published by Begell House Inc. Publishers in Journal of Environmental Pathology, Toxicology and Oncology
- Vol. 43 (2) , 57-76
Role of Alpha-Fetoprotein in the Pathogenesis of Cancer
Alpha-fetoprotein (AFP) belongs to the albuminoid protein family and is considered as the fetal analog of serum albumin. This plasma protein is initially synthesized in the fetal liver and yolk sac and shows a maximum peak near the end of the first trimester. Later, concentrations begin to decline prenatally and drop precipitously after birth. This protein has three key ligand-binding pockets for interactions with various biomolecules. It contains multiple phosphorylation and acetylation sites for the regulation of physiological and pathophysiological states. High serum AFP titer is an established biomarker for yolk sac, embryonal and hepatocellular carcinoma. The present review critically analyzes the chemical nature, receptors, clinical implications, and therapeutic aspects of AFP, underpinning the development of different types of cancer.
- 1 January 2024
- Published by Begell House Inc. Publishers in Journal of Environmental Pathology, Toxicology and Oncology
- Vol. 43 (2) , 57-76
Role of Alpha-Fetoprotein in the Pathogenesis of Cancer
Alpha-fetoprotein (AFP) belongs to the albuminoid protein family and is considered as the fetal analog of serum albumin. This plasma protein is initially synthesized in the fetal liver and yolk sac and shows a maximum peak near the end of the first trimester. Later, concentrations begin to decline prenatally and drop precipitously after birth. This protein has three key ligand-binding pockets for interactions with various biomolecules. It contains multiple phosphorylation and acetylation sites for the regulation of physiological and pathophysiological states. High serum AFP titer is an established biomarker for yolk sac, embryonal and hepatocellular carcinoma. The present review critically analyzes the chemical nature, receptors, clinical implications, and therapeutic aspects of AFP, underpinning the development of different types of cancer.
- 6 November 2023
- Published by Sciencedomain International in Asian Journal of Environment & Ecology
- Vol. 22 (4) , 148-164
Missing the Dark: Malediction for the Environment and Human Health
Modern civilization has flourished after the invention of electricity and eclectic lights for getting illumination at night. Initially, artificial light was a blessing for the civilization and mankind. Later, artificial-light-at-night (ALAN) appears as a serious problem in our modern world. Rapid urbanization and industrialization are the major causes of light pollution. Indeed, artificial light has several benefits, but it has negative impacts on the entire living system, including humans. Nighttime light exposure disrupts circadian clock activities and deregulates many rhythmic behaviors (sleep, hormone secretion, and others). Insects, fishes, frogs, turtles, birds, nocturnal mammals (bats and rats), and humans are facing serious problems. Light pollution alters behavioral functions, physical and physiological activities, feeding and nesting behavior, migration, and reproductive functions in different animals. Shift work, night work, and lit areas in the streets and residential areas make a serious issue for human exposure and may cause several pathologies. Thus ALAN affects entire ecosystems, and the present review focuses on the effects of light pollution on the different living systems.
- 6 November 2023
- Published by Sciencedomain International in Asian Journal of Environment & Ecology
- Vol. 22 (4) , 148-164
Missing the Dark: Malediction for the Environment and Human Health
Modern civilization has flourished after the invention of electricity and eclectic lights for getting illumination at night. Initially, artificial light was a blessing for the civilization and mankind. Later, artificial-light-at-night (ALAN) appears as a serious problem in our modern world. Rapid urbanization and industrialization are the major causes of light pollution. Indeed, artificial light has several benefits, but it has negative impacts on the entire living system, including humans. Nighttime light exposure disrupts circadian clock activities and deregulates many rhythmic behaviors (sleep, hormone secretion, and others). Insects, fishes, frogs, turtles, birds, nocturnal mammals (bats and rats), and humans are facing serious problems. Light pollution alters behavioral functions, physical and physiological activities, feeding and nesting behavior, migration, and reproductive functions in different animals. Shift work, night work, and lit areas in the streets and residential areas make a serious issue for human exposure and may cause several pathologies. Thus ALAN affects entire ecosystems, and the present review focuses on the effects of light pollution on the different living systems.