P. Vineeth Daniel

ORCID: 0000-0002-2612-9043
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About
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Research Areas
  • Liver Disease Diagnosis and Treatment
  • Advanced Glycation End Products research
  • Cholesterol and Lipid Metabolism
  • Lipid metabolism and disorders
  • Alcohol Consumption and Health Effects
  • Pancreatic function and diabetes
  • Biochemical effects in animals
  • Endoplasmic Reticulum Stress and Disease
  • Wastewater Treatment and Reuse
  • Metabolism, Diabetes, and Cancer
  • Folate and B Vitamins Research
  • Analytical Chemistry and Sensors
  • Peroxisome Proliferator-Activated Receptors
  • Sphingolipid Metabolism and Signaling
  • Neuropeptides and Animal Physiology
  • Lanthanide and Transition Metal Complexes
  • TiO2 Photocatalysis and Solar Cells
  • Sulfur Compounds in Biology
  • Diet, Metabolism, and Disease
  • S100 Proteins and Annexins
  • Phagocytosis and Immune Regulation
  • Receptor Mechanisms and Signaling
  • Luminescence and Fluorescent Materials
  • Diabetes Treatment and Management
  • Cannabis and Cannabinoid Research

Mayo Clinic in Arizona
2023-2025

Mayo Clinic
2024

WinnMed
2024

Indian Institute of Technology Mandi
2017-2022

Intrahepatic macrophages in nonalcoholic steatohepatitis (NASH) are heterogenous and include proinflammatory recruited monocyte derived macrophages. The receptor for advanced glycation end products (RAGE) is expressed on can be activated by damage associated molecular patterns (DAMPs) upregulated NASH, yet the role of macrophage-specific RAGE signaling NASH unclear. Therefore, we hypothesized that expressing mediate liver inflammation NASH. Compared to healthy controls, expression was...

10.1172/jci.insight.169138 article EN cc-by JCI Insight 2024-01-04

Immune cell-driven inflammation is a key mediator of metabolic dysfunction-associated steatohepatitis (MASH) progression. We have previously demonstrated that pharmacological sphingosine 1-phosphate (S1P) receptor modulation ameliorates MASH and associated with attenuated accumulation intrahepatic macrophage T-cell subsets. Although S1P receptors are expressed on several immune cell types, given the prominent role monocyte-derived recruited macrophages in sterile MASH, we hypothesized...

10.1097/hc9.0000000000000613 article EN cc-by-nc-nd Hepatology Communications 2025-02-01

Development of a highly photostable, renal clearable, and nontoxic new NIR probe (CyG) for precise quantification albumin in different biofluids liver targeted vivo visualization is demonstrated. CyG's inherent property to interact selectively with among biomolecules intracellular environment high degree sensitivity helps CyG imaging. In addition its long excitation/emission wavelengths (λex = 740 nm, λem 804 nm), which are much above the biological tissue opaque window (400-700 nm) ensuring...

10.1021/acs.analchem.7b02187 article EN Analytical Chemistry 2017-08-21

Overconsumption of sucrose and other sugars has been associated with nonalcoholic fatty liver disease (NAFLD). Reports suggest hepatic de novo lipogenesis (DNL) as an important contributor to regulator carbohydrate-induced lipid accumulation in NAFLD. The mechanisms responsible for the increase DNL due overconsumption carbohydrate diet are less than clear; however, literatures high activate lipogenic transcription factor response element-binding protein (ChREBP), which further transcribes...

10.1016/j.jbc.2021.100714 article EN cc-by Journal of Biological Chemistry 2021-01-01

The glucagon-like peptide-1 receptor (GLP-1R) is a well-known target of therapeutics industries for the treatment various metabolic diseases like type 2 diabetes and obesity. structural–functional relationships small molecule agonists GLP-1R are yet to be understood. Therefore, an attempt was made on structurally known (Compound 1, Compound 2, A, B, (S)-8) study their interaction with extracellular domain GLP-1R. In this study, we explored dynamics, intrinsic stability, binding mechanisms...

10.1080/07391102.2018.1532818 article EN Journal of Biomolecular Structure and Dynamics 2018-10-09

Apolipoprotein H (APOH) downregulation can cause hepatic steatosis and gut microbiota dysbiosis. However, the mechanism by which APOH-regulated lipid metabolism contributes to metabolic dysfunction-associated steatotic liver disease (MASLD) remains undetermined. Herein, we aim explore regulatory effect of APOH, mediated through various pathways, on homeostasis MASLD pathogenesis. We analyzed serum marker levels, histopathology, cholesterol metabolism-related gene expression in global ApoH

10.1016/j.jlr.2023.100483 article EN cc-by Journal of Lipid Research 2023-12-14

Dysregulated hepatic de novo lipogenesis contributes to the pathogenesis of nonalcoholic fatty liver disease in both humans and rodents. Clinical evidence suggests have a positive correlation with serum lead (Pb 2+ ) levels. However, an exact mechanism Pb ‐induced progression is still unknown. Here, we show that exposure regulates Ch REBP ‐dependent lipogenesis. Presence ions within hepatocytes reduces transcript protein levels sorcin, cytosolic adaptor partner . Adenovirus‐mediated...

10.1002/1873-3468.13538 article EN FEBS Letters 2019-07-16

Nonalcoholic fatty liver disease (NAFLD) is an independent predictor of systemic insulin resistance and type 2 diabetes mellitus (T2DM). However, converse correlates between excess fat content β-cell function remain equivocal. Specifically, how the accumulation consequent to enhanced de novo lipogenesis (DNL) leads pancreatic failure eventually T2DM elusive. Here, we have identified that low-molecular-weight calcium-binding protein S100A6, or calcyclin, inhibits glucose-stimulated secretion...

10.2337/db22-0056 article EN Diabetes 2022-07-28

We demonstrate a strategy for the recognition of As5+ in aqueous solution using red-emissive probe based on perylene-Cu2+ ensemble decorated with peripheral free carboxyl functionality. Single crystal analysis helped us to understand chemical structure probe. To best our knowledge, this is first arsenic detection which emits red region (λem = 600 nm). The exhibited mega-Stokes shift (>100 nm) high degree selectivity upon interaction As5+, indicated that present has potential be used as...

10.1039/c7dt02387a article EN Dalton Transactions 2017-01-01

Type 2 diabetes mellitus (T2DM) is a metabolic disease characterized by reduced insulin sensitivity and dysfunction of β-cells. Although the increasing prevalence worldwide largely attributed to genetic predisposition or lifestyle factors (insufficient physical activity), caloric intake. Environmental factors, exposure xenobiotics heavy metals have also been reported be causative T2DM. At this juncture, we, through our work unveil plausible link between Pb2+ mellitus, delineated...

10.1093/toxres/tfab121 article EN Toxicology Research 2021-12-02

<p>Nonalcoholic fatty liver disease (NAFLD) is an independent predictor of systemic insulin resistance and type 2 diabetes mellitus (T2DM). However, converse correlates between excess fat content β-cell function remain equivocal. Specifically, how the accumulation consequent to enhanced <em>de novo</em> lipogenesis (DNL) leads pancreatic failure eventually T2DM elusive. Here we have identified low-molecular-weight calcium-binding protein S100A6 or calcyclin inhibits...

10.2337/figshare.20361846 preprint EN cc-by-nc-sa 2022-07-28

<p>Nonalcoholic fatty liver disease (NAFLD) is an independent predictor of systemic insulin resistance and type 2 diabetes mellitus (T2DM). However, converse correlates between excess fat content β-cell function remain equivocal. Specifically, how the accumulation consequent to enhanced <em>de novo</em> lipogenesis (DNL) leads pancreatic failure eventually T2DM elusive. Here we have identified low-molecular-weight calcium-binding protein S100A6 or calcyclin inhibits...

10.2337/figshare.20361846.v1 preprint EN cc-by-nc-sa 2022-07-28
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