Ethanol-Induced Hepatotoxicity and Alcohol Metabolism Regulation by GABA-Enriched Fermented Smilax china Root Extract in Rats

Chronic alcohol consumption can cause hepatic injury and alcohol-induced toxicities. Extracts from Smilax china root have been widely used in traditional medicine and for their potential pharmacological benefits. We aimed to determine if fermented Smilax china extract (FSC) regulates alcoholic fatty liver and liver injury using two in vivo experiments. Sprague-Dawley rats were administered ethanol (3 g/kg b.w.; po) with or without FSC pretreatment to induce an acute hangover. In another experiment, rats were fed either a normal or Lieber-DeCarli ethanol (6.7%) diet with or without FSC pretreatment (125, 250, and 500 mg/kg b.w.; po) for 28 days. Serum biomarkers, liver histopathology, and the mRNA levels of anti-inflammatory, antioxidant, lipogenic, and lipolytic genes were analyzed. FSC pretreatment significantly reduced blood alcohol and acetaldehyde concentrations, upregulated the mRNA expression of alcohol dehydrogenase, aldehyde dehydrogenase, and superoxide dismutase, and decreased the activities of liver enzymes in a dose-dependent manner. It also downregulated SERBP-1c and upregulated PPAR-α and reduced the gene expression of the anti-inflammatory cytokine IL-6 in the liver. The final extract after fermentation had increased GABA content. Furthermore, FSC was found to be safe with no acute oral toxicity in female rats. Thus, FSC increases alcohol metabolism and exhibits antioxidant and anti-inflammatory effects to induce hepatoprotection against alcohol-induced damage. It may be used as a functional food ingredient after excess alcohol consumption.

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Vasoactive Intestinal Peptide Modulation of the Steroid-Induced LH Surge Involves Kisspeptin Signaling in Young but Not in Middle-Aged Female Rats

Endocrinology ◽

10.1210/en.2013-1793 ◽

2014 ◽

Vol 155 (6) ◽

pp. 2222-2232 ◽

Cited By ~ 10

Author(s):

Alexander S. Kauffman ◽

Yan Sun ◽

Joshua Kim ◽

Azim R. Khan ◽

Jun Shu ◽

...

Keyword(s):

Vasoactive Intestinal Peptide ◽

Suprachiasmatic Nucleus ◽

Reproductive Age ◽

Female Rats ◽

Mrna Levels ◽

Dependent Manner ◽

Middle Aged ◽

Lh Surge ◽

Young Females ◽

Gnrh Neurons

Age-related LH surge dysfunction in middle-aged rats is characterized, in part, by reduced responsiveness to estradiol (E2)-positive feedback and reduced hypothalamic kisspeptin neurotransmission. Vasoactive intestinal peptide (VIP) neurons in the suprachiasmatic nucleus project to hypothalamic regions that house kisspeptin neurons. Additionally, middle-age females express less VIP mRNA in the suprachiasmatic nucleus on the day of the LH surge and intracerebroventricular (icv) VIP infusion restores LH surges. We tested the hypothesis that icv infusion of VIP modulates the LH surge through effects on the kisspeptin and RFamide-related peptide-3 (RFRP-3; an estradiol-regulated inhibitor of GnRH neurons) neurotransmitter systems. Brains were collected for in situ hybridization analyses from ovariectomized and ovarian hormone-primed young and middle-aged females infused with VIP or saline. The percentage of GnRH and Kiss1 cells coexpressing cfos and total Kiss1 mRNA were reduced in saline-infused middle-aged compared with young females. In young females, VIP reduced the percentage of GnRH and Kiss1 cells coexpressing cfos, suggesting that increased VIP signaling in young females adversely affected the function of Kiss1 and GnRH neurons. In middle-aged females, VIP increased the percentage of GnRH but not Kiss1 neurons coexpressing cfos, suggesting VIP affects LH release in middle-aged females through kisspeptin-independent effects on GnRH neurons. Neither reproductive age nor VIP affected Rfrp cell number, Rfrp mRNA levels per cell, or coexpression of cfos in Rfrp cells. These data suggest that VIP differentially affects activation of GnRH and kisspeptin neurons of female rats in an age-dependent manner.

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Antioxidant and Anti-inflammatory Protective Properties of Thai Shallot (Allium ascalonicum cv. Chiangmai) Juice on Human Vascular Endothelial Cell Lines (EA.hy926)

Walailak Journal of Science and Technology (WJST) ◽

10.48048/wjst.2019.6222 ◽

2019 ◽

Vol 16 (3) ◽

pp. 175-184

Author(s):

Sakaewan OUNJAIJEAN ◽

Sukanya CHACHIYO ◽

Kanokwan KULPRACHAKARN ◽

Kongsak BOONYAPRANAI ◽

Somdet SRICHAIRATANAKOOL ◽

...

Keyword(s):

Oxidative Stress ◽

Endothelial Cell ◽

Vascular Endothelial Cell ◽

Membrane Lipid ◽

Dependent Manner ◽

Vascular Endothelial ◽

Ros Production ◽

Food Ingredient ◽

Human Vascular Endothelial Cell ◽

Anti Inflammatory

Oxidative stress and inflammation are 2 major contributors to numerous life-threatening disorders, including vascular pathologies. Shallots (Allium ascalonicum) are a type of red onion which grows in Southeast Asia. Bulbs of this plant are used both as a food ingredient and in traditional medicine. This study attempted to investigate the possible ways that juice extracted from Thai shallot (A.ascalonicum cv. Chiangmai) bulbs could be used in the prevention of cardiovascular complications. The antioxidative and anti-inflammatory effects of shallot juice extract (SHE) on human vascular endothelial cells (EA.hy926) were investigated. Cell viability was evaluated by MTT assay, membrane lipid peroxidation by thiobarbituric acid reactive substances assay, intracellular reactive oxygen species (ROS) production by the fluorescent probe 6-carboxy-2'-7'-dichlorofluoresceine, and interleukin-6 (IL-6) released by ELISA. The shallot juice showed extremely low cytotoxicity against EA.hy926 cells, with IC50 of 41.9 and 27.3 mg/ml for 24 h- and 48 h-incubation, respectively. SHE reduced the iron-induced malondialdehyde production in a dose-dependent manner. The extract also demonstrated antioxidant activity as shown by a significant reduction of H2O2-induced ROS production at a low concentration (< 200 mg/ml). Furthermore, SHE significantly attenuated the level of IL-6 released during lipopolysaccharide stimulation (p < 0.05). It is of interest that the juice extracted from Thai shallot bulbs demonstrated both cellular antioxidant and anti-inflammatory properties in endothelial cell models, combined with a reduction in toxicity. Shallot extract could be considered as a nutraceutical for the prevention or management of vascular diseases as it is related to oxidative stress and inflammation.

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Phytochemical Profile, Free Radical Scavenging and Anti-Inflammatory Properties of Acalypha Indica Root Extract: Evidence from In Vitro and In Vivo Studies

Molecules ◽

10.3390/molecules26206251 ◽

2021 ◽

Vol 26 (20) ◽

pp. 6251

Author(s):

Ravi Sahukari ◽

Jyothi Punabaka ◽

Shanmugam Bhasha ◽

Venkata Subbaiah Ganjikunta ◽

Shanmugam Kondeti Ramudu ◽

...

Keyword(s):

Free Radical ◽

Radical Scavenging ◽

Free Radical Scavenging ◽

In Vivo Studies ◽

Root Extract ◽

Dependent Manner ◽

Anti Inflammatory ◽

Acalypha Indica

In our in vitro and in vivo studies, we used Acalypha indica root methanolic extract (AIRME), and investigated their free radical scavenging/antioxidant and anti-inflammatory properties. Primarily, phytochemical analysis showed rich content of phenols (70.92 mg of gallic acid/g) and flavonoids (16.01 mg of rutin/g) in AIRME. We then performed HR-LC-MS and GC-MS analyses, and identified 101 and 14 phytochemical compounds, respectively. Among them, ramipril glucuronide (1.563%), antimycin A (1.324%), swietenine (1.134%), quinone (1.152%), oxprenolol (1.118%), choline (0.847%), bumetanide (0.847%) and fenofibrate (0.711%) are the predominant phytomolecules. Evidence from in vitro studies revealed that AIRME scavenges DPPH and hydroxyl radicals in a concentration dependent manner (10–50 μg/mL). Similarly, hydrogen peroxide and lipid peroxidation were also remarkably inhibited by AIRME as concentration increases (20–100 μg/mL). In vitro antioxidant activity of AIRME was comparable to ascorbic acid treatment. For in vivo studies, carrageenan (1%, sub-plantar) was injected to rats to induce localized inflammation. Acute inflammation was represented by paw-edema, and significantly elevated (p < 0.05) WBC, platelets and C-reactive protein (CRP). However, AIRME pretreatment (150/300 mg/kg bodyweight) significantly (p < 0.05) decreased edema volume. This was accompanied by a significant (p < 0.05) reduction of WBC, platelets and CRP with both doses of AIRME. The decreased activities of superoxide dismutase, catalase, glutathione reductase and glutathione peroxidase in paw tissue were restored (p < 0.05 / p < 0.01) with AIRME in a dose-dependent manner. Furthermore, AIRME attenuated carrageenan-induced neutrophil infiltrations and vascular dilation in paw tissue. For the first time, our findings demonstrated the potent antioxidant and anti-inflammatory properties of AIRME, which could be considered to develop novel anti-inflammatory drugs.

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Allium porrum Extract Decreases Effector Cell Degranulation and Modulates Airway Epithelial Cell Function

Nutrients ◽

10.3390/nu11061303 ◽

2019 ◽

Vol 11 (6) ◽

pp. 1303 ◽

Cited By ~ 1

Author(s):

Sara Benedé ◽

Ana Gradillas ◽

Mayte Villalba ◽

Eva Batanero

Keyword(s):

Cell Function ◽

Total Phenolic ◽

Allium Porrum ◽

Mrna Levels ◽

Dependent Manner ◽

Airway Epithelial ◽

Allergy Treatment ◽

Lower Permeability ◽

Anti Inflammatory ◽

High Concentrations

Allium genus plants, such as leek (Allium porrum), are rich sources of anti-inflammatory and anti-oxidant secondary metabolites; this is of interest because it demonstrates their suitability as pharmacological alternatives for inflammatory processes, including allergy treatment. The composition of methanolic leek extract (LE) was analyzed by GC–MS and LC–IT/MS, and the total phenolic content and antioxidant capacity were quantified by colorimetric methods. Its pharmacological potential was analyzed in human bronchial epithelial Calu-3 cells, human mast cells LAD2, and humanized rat basophiles RBL-2H3. LE exhibited a cytotoxic effect on Calu-3 cells and HumRBL-2H3 cells only at high concentrations and in a dose-dependent manner. Moreover, LE decreased the degranulation of LAD2 and HumRBL-2H3 cells. LE treatment also significantly prevented alterations in transepithelial electrical resistance values and mRNA levels of glutathione-S-transferase (GST), c-Jun, and NFκB after treatment with H2O2 in ALI-cultured Calu-3 cells. Finally, ALI-cultured Calu-3 cells treated with LE showed lower permeability to Ole e 1 compared to untreated cells. A reduction in IL-6 secretion in ALI-cultured Calu-3 cells treated with LE was also observed. In summary, the results obtained in this work suggest that A. porrum extract may have potential anti-allergic effects due to its antioxidant and anti-inflammatory properties. This study provides several important insights into how LE can protect against allergy.

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PHYTOCHEMICAL ANALYSIS AND IN VITRO STUDIES ON ANTIBACTERIAL, ANTIOXIDANT AND ANTI-INFLAMMATORY ACTIVITIES USING CASUARINA EQUISETIFOLIA BARK EXTRACTS

International Journal of Pharmacy and Pharmaceutical Sciences ◽

10.22159/ijpps.2018v10i1.22188 ◽

2018 ◽

Vol 10 (1) ◽

pp. 118

Author(s):

Saranya V. T. K. ◽

S. Uma Gowrie

Keyword(s):

Secondary Metabolites ◽

Tree Species ◽

Forest Tree ◽

Root Extract ◽

Dependent Manner ◽

Casuarina Equisetifolia ◽

Forest Tree Species ◽

Ms Analysis ◽

Anti Inflammatory

Objective: Casuarina equisetifolia is an important multipurpose exotic forest tree species widely cultivated in the coastal regions of Tamil Nadu that serves as a warehouse of essential secondary metabolites. Identification of these bioactive compounds in this forest tree species might lead to the discovery and development of a new drug to treat various diseases. Methods: The present study was carried out with an objective to analyse the phytochemicals qualitatively and quantitatively. Gas Chromatography-Mass Spectrometry (GC-MS) analysis was performed to evaluate the presence of various volatile compounds. An in vitro antibacterial, antioxidant and anti-inflammatory properties of aqueous and organic solvents of C. equisetifolia bark was studied.Results: The preliminary qualitative screening revealed the presence of alkaloids, glycosides, carbohydrates, proteins, flavonoids, phenols, terpenoids, and tannins. The quantitative analysis revealed the presence of maximum phenols (71.2±0.51 mg/g), flavonoids (35.12±0.34 mg/g), tannins (77.59±0.21) and terpenoids (6%) in methanolic root extract with respective standards. Several peaks were obtained in the GC-MS analysis which indicates the presence of different secondary metabolites. Antibacterial activity showed a maximum zone of inhibition against Escherichia coli (23±0.24 mm) and Proteus vulgaris (23±0.32 mm). The antioxidant potential of various extracts was compared with the standard ascorbic acid. Anti-inflammatory activity was compared with standard diclofenac sodium and the extract showed activities significantly in a dose-dependent manner. Conclusion: From this study, it is revealed that C. equisetifolia bark extract possesses efficient antibacterial property, the potential in scavenging free radical, effective antioxidant, powerful anti-inflammatory source that can be employed in the development of a novel drug to treat various diseases.

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POTENT BIOACTIVE METABOLITES OF CASUARINA JUNGHUHNIANA MIQ. ROOTS–A THERAPEUTIC APPROACH

International Journal of Pharmacy and Pharmaceutical Sciences ◽

10.22159/ijpps.2017v9i3.16264 ◽

2017 ◽

Vol 9 (3) ◽

pp. 158

Author(s):

Chathurdevi G. ◽

S. Umagowrie

Keyword(s):

Secondary Metabolites ◽

Therapeutic Approach ◽

Protein Denaturation ◽

Bioactive Metabolites ◽

Diffusion Method ◽

Root Extract ◽

Symbiotic Association ◽

Dependent Manner ◽

Anti Inflammatory ◽

Promising Source

Objective: Casuarina junghuhniana Miq. is a multipurpose tree, belongs to the family Casuarinaceae. It has a symbiotic association with actinomycete Frankia which makes the tree to grow vigorously on varied environmental conditions. Not much work has been documented on secondary metabolites and therapeutic approach of this species in India. Therefore, the objective of the present study was to explore the potential phytochemicals in the root extracts and its therapeutic values.Methods: Casuarina junghuhniana root samples were collected from the State Forest Research Institute, Kolappakam, Chennai. The qualitative and quantitative phytochemicals screening were carried out using standard procedures. Antibacterial assay was tested against different pathogens using well diffusion method. Antioxidant activity was carried out using reducing power, hydrogen peroxide scavenging and 1, 1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging methods. The anti-inflammatory assay was tested using protein denaturation method. Further, the phytochemicals in the root extract were evaluated using GC-MS studies. The functional role of the phytoconstituent was confirmed by docking against the target using mcule software.Results: The qualitative screening revealed the presence of various phytoconstituents. The quantitative analysis revealed the presence of maximum phenols (68.95±0.46 mg/g), flavonoids (34.15±0.33 mg/g) and terpenoids (3.9%) in methanolic root extract with respective standards. Antibacterial activity showed a maximum zone of inhibition against Bacillus subtilis (19±0.2 mm) followed by Staphylococcus sp (14±0.3 mm). The antioxidant and anti-inflammatory activity was compared with standard ascorbic acid and the extract showed activities in a dose-dependent manner. Several peaks were obtained in the GC-MS analysis which indicates the presence of different secondary metabolites. The specific phytocompound showed prominent binding affinity against the target enzyme in docking studies.Conclusion: The presence of potent phytochemicals in the Casuarina junghuhniana root with antioxidant and anti-inflammatory activities could be used as a promising source for developing novel plant-based therapeutic agents.

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Quercetin Inhibits Inflammatory Response Induced by LPS from Porphyromonas gingivalis in Human Gingival Fibroblasts via Suppressing NF-κB Signaling Pathway

BioMed Research International ◽

10.1155/2019/6282635 ◽

2019 ◽

Vol 2019 ◽

pp. 1-10 ◽

Cited By ~ 4

Author(s):

Gang Xiong ◽

Wansheng Ji ◽

Fei Wang ◽

Fengxiang Zhang ◽

Peng Xue ◽

...

Keyword(s):

Porphyromonas Gingivalis ◽

Interleukin 1 ◽

Human Gingival Fibroblasts ◽

Enzyme Linked Immunosorbent Assay ◽

Peroxisome Proliferator ◽

Mrna Levels ◽

Dependent Manner ◽

Gingival Fibroblasts ◽

Peroxisome Proliferator Activated Receptor ◽

Anti Inflammatory

Quercetin, a natural flavonol existing in many food resources, has been reported to be an effective antimicrobial and anti-inflammatory agent for restricting the inflammation in periodontitis. In this study, we aimed to investigate the anti-inflammatory effects of quercetin on Porphyromonas gingivalis (P. gingivalis) lipopolysaccharide- (LPS-) stimulated human gingival fibroblasts (HGFs). HGFs were pretreated with quercetin prior to LPS stimulation. Cell viability was evaluated by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay. The levels of inflammatory cytokines, including interleukin-1β (IL-1β), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α), along with chemokine interleukin-8 (IL-8), were determined by enzyme-linked immunosorbent assay (ELISA). The mRNA levels of IL-1β, IL-6, IL-8, TNF-α, IκBα, p65 subunit of nuclear factor-kappa B (NF-κB), peroxisome proliferator-activated receptor-γ (PPAR-γ), liver X receptor α (LXRα), and Toll-like receptor 4 (TLR4) were measured by real-time quantitative PCR (RT-qPCR). The protein levels of IκBα, p-IκBα, p65, p-p65, PPAR-γ, LXRα, and TLR4 were characterized by Western blotting. Our results demonstrated that quercetin inhibited the LPS-induced production of IL-1β, IL-6, IL-8, and TNF-α in a dose-dependent manner. It also suppressed LPS-induced NF-κB activation mediated by TLR4. Moreover, the anti-inflammatory effects of quercetin were reversed by the PPAR-γ antagonist of GW9662. In conclusion, these results suggested that quercetin attenuated the production of IL-1β, IL-6, IL-8, and TNF-α in P. gingivalis LPS-treated HGFs by activating PPAR-γ which subsequently suppressed the activation of NF-κB.

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EVALUATION OF ETHANOLIC ROOT EXTRACT OF PARTHENIUM HYSTEROPHORUS LINN FOR ANTIOXIDANT AND ANTI-INFLAMMATORY ACTIVITY

International Journal of Current Pharmaceutical Research ◽

10.22159/ijcpr.2017v9i5.22327 ◽

2017 ◽

pp. 194-197 ◽

Cited By ~ 1

Author(s):

Pankaj Lohumi ◽

Tirath Kumar ◽

Lipi Nogai

Keyword(s):

Nitric Oxide ◽

Radical Scavenging ◽

Reducing Power ◽

Parthenium Hysterophorus ◽

Inflammatory Activity ◽

Root Extract ◽

Dependent Manner ◽

Concentration Dependent Manner ◽

Soxhlet Apparatus ◽

Anti Inflammatory

Objective: The work is aimed to draw out the health beneficial properties of a weed (Parthenium hysterophorus Linn). The present work is organized to evaluate the antioxidant and anti-inflammatory activity of the ethanolic root extract of Parthenium hysterophorus Linn.Methods: In the present work the ethanolic extract was determined by using soxhlet apparatus. The antioxidant scavenging activity of this extract was determined by applying three different assay methods: (1) DPPH (1, 1-diphenyl-2-picryl hydrazyl) free radical method. (2) Nitric oxide scavenging assay and (3) Reducing power method. The anti-inflammatory activity was determined by in vivo method i.e. Carrageenan induced rat paw edema.Results: DPPH radical scavenging activities of the standard antioxidant and extracts were found to be increased in dose dependent manner. The percentage inhibition increases from 4.19% to 97.09% within the concentration range of 10Âµg/ml to 160Âµg/ml. Parthenium hysterophorus Linn effectively reduced the generation of nitric oxide radicals from sodium nitroprusside solution in a concentration dependent manner and percentage inhibition increases from 3.53% to 55.21% within the concentration range 10Âµg/ml to 160Âµg/ml. All the concentrations of extract significantly showed higher absorbance than the absorbance of control reaction (0.9705) in reducing power assay. A Higher absorbance indicates high reducing power due to the formation of reduced intermediates. Parthenium hysterophorus Linn showed highly significant anti-inflammatory activity at a dose of 200 mg/kg and the lesser effect was observed at 100 mg/kg with the percentage change in paw volume at 0 min, 30 min, 60 min, 90 min and 120 min.Conclusion: Thus, from above experimental observations, it can be stated that Parthenium is a natural antioxidant and bearing anti-inflammatory activity.Â

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Anti-inflammatory dihydroxanthones from a Diaporthe species

Biological Chemistry ◽

10.1515/hsz-2021-0192 ◽

2021 ◽

Vol 0 (0) ◽

Author(s):

Markus Rohr ◽

Anna Maria Kiefer ◽

Ulrich Kauhl ◽

Jonathan Groß ◽

Till Opatz ◽

...

Keyword(s):

Density Functional ◽

Promoter Activity ◽

Inflammatory Marker ◽

Marker Gene ◽

Mrna Levels ◽

Dependent Manner ◽

Cytokines And Chemokines ◽

Anti Inflammatory ◽

Inducible Protein ◽

Nfκb Pathway

Abstract In a search for anti-inflammatory compounds from fungi inhibiting the promoter activity of the small chemokine CXCL10 (Interferon-inducible protein 10, IP-10) as a pro-inflammatory marker gene, the new dihydroxanthone methyl (1R, 2R)-1,2,8-trihydroxy-6-(hydroxymethyl)-9-oxo-2,9-dihydro-1H-xanthene-1-carboxylate (2) and the previously described dihydroxanthone AGI-B4 (1) were isolated from fermentations of a Diaporthe species. The structures of the compounds were elucidated by a combination of one- and two-dimensional NMR spectroscopy, mass spectrometry, and calculations using density functional theory (DFT). Compounds 1 and 2 inhibited the LPS/IFNγ induced CXCL10 promoter activity in transiently transfected human MonoMac6 cells in a dose-dependent manner with IC50 values of 4.1 µM (±0.2 µM) and 1.0 µM (±0.06 µM) respectively. Moreover, compounds 1 and 2 reduced mRNA levels and synthesis of pro-inflammatory mediators such as cytokines and chemokines in LPS/IFNγ stimulated MonoMac6 cells by interfering with the Stat1 and NFκB pathway.

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Curcumin Reduces Hepatic and White Adipose Tissue Inflammation and Expression of Specific Zinc Transporters in Diet-Induced Obese Mice

Current Developments in Nutrition ◽

10.1093/cdn/nzab037_035 ◽

2021 ◽

Vol 5 (Supplement_2) ◽

pp. 325-325

Author(s):

Tariful Islam ◽

Geetika Katasani ◽

Iurii Koboziev ◽

Kembra Albracht-Schulte ◽

Shane Scoggin ◽

...

Keyword(s):

Adipose Tissue ◽

White Adipose Tissue ◽

Inflammatory Markers ◽

Zinc Homeostasis ◽

Metabolic Effects ◽

Zinc Transporters ◽

Whole Body ◽

Mrna Levels ◽

Alcoholic Fatty Liver ◽

Anti Inflammatory

Abstract Objectives Obesity is a complex metabolic disease, that is often associated with non-alcoholic fatty liver disease (NAFLD). Inflammation is a common feature of both diseases. Curcumin, a traditionally used spice in Asia, exerts anti-inflammatory effects in liver and white adipose tissue (WAT) of diet-induced obese (DIO) mice. However, mechanisms involved in these beneficial effects remain obscure. Zinc is an important micronutrient involved in inflammatory responses. Whole-body zinc homeostasis plays a critical role in decreasing tissue specific inflammation. Zinc homeostasis is maintained mainly by zinc transporters known as ZnT (zinc transporters) and Zip (Zrt and Irt-like proteins) family. We propose that zinc transporters may contribute to curcumin's protective metabolic effects. Thus, the objective of this research was to determine curcumin's effects on inflammatory markers and zinc transporters in liver and WAT from DIO mice. Methods Male B6 mice were fed a HFD (45% kcal fat) or HFD supplemented with 0.4% (w/w) curcumin (HFC) for fourteen weeks. Serum triglycerides (TG) and free fatty acid (FFA) levels were measured. mRNA levels for inflammatory markers and zinc transporters were determined in WAT and liver by qRT-PCR. Results No significant changes were observed in body weight, serum TG and FFA levels with curcumin supplementation. However, gene expression of inflammatory markers, including Stat1, and Nf-KB subunit p65 were significantly reduced in liver and WAT from HFC group compared to HF (P < 0.05). Furthermore, curcumin reduced hepatic zinc transporters Zip10, Zip14, ZnT10 but increased ZnT9 expression. In WAT, curcumin significantly reduced mRNA levels for Zip1, Zip14, ZnT1, and ZnT7 (P < 0.05). Conclusions Our results indicate that zinc transporters may in part mediate the anti-inflammatory properties of curcumin, particularly Zip14, in WAT and liver of DIO mice. Future mechanistic studies are necessary to establish whether zinc transporters are required for curcumin's anti-inflammatory effects in obesity and associated NAFLD. Funding Sources AHA grant# 19AIREA34450279.

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