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  1. Article: Bio-electrospraying assessment toward in situ chondrocyte-laden electrospun scaffold fabrication.

    Semitela, Ângela / Ramalho, Gonçalo / Capitão, Ana / Sousa, Cátia / Mendes, Alexandrina F / Aap Marques, Paula / Completo, António

    Journal of tissue engineering

    2022  Volume 13, Page(s) 20417314211069342

    Abstract: Electrospinning has been widely used to fabricate fibrous scaffolds for cartilage tissue engineering, but their small pores severely restrict cell infiltration, resulting in an uneven distribution of cells across the scaffold, particularly in three- ... ...

    Abstract Electrospinning has been widely used to fabricate fibrous scaffolds for cartilage tissue engineering, but their small pores severely restrict cell infiltration, resulting in an uneven distribution of cells across the scaffold, particularly in three-dimensional designs. If bio-electrospraying is applied, direct chondrocyte incorporation into the fibers during electrospinning may be a solution. However, before this approach can be effectively employed, it is critical to identify whether chondrocytes are adversely affected. Several electrospraying operating settings were tested to determine their effect on the survival and function of an immortalized human chondrocyte cell line. These chondrocytes survived through an electric field formed by low needle-to-collector distances and low voltage. No differences in chondrocyte viability, morphology, gene expression, or proliferation were found. Preliminary data of the combination of electrospraying and polymer electrospinning disclosed that chondrocyte integration was feasible using an alternated approach. The overall increase in chondrocyte viability over time indicated that the embedded cells retained their proliferative capacity. Besides the cell line, primary chondrocytes were also electrosprayed under the previously optimized operational conditions, revealing the higher sensitivity degree of these cells. Still, their post-electrosprayed viability remained considerably high. The data reported here further suggest that bio-electrospraying under the optimal operational conditions might be a promising alternative to the existent cell seeding techniques, promoting not only cells safe delivery to the scaffold, but also the development of cellularized cartilage tissue constructs.
    Language English
    Publishing date 2022-01-08
    Publishing country England
    Document type Journal Article
    ZDB-ID 2573915-3
    ISSN 2041-7314
    ISSN 2041-7314
    DOI 10.1177/20417314211069342
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Expression and function of the nonclassical estrogen receptor, GPR30, in human cartilage and chondrocytes.

    Ribeiro, Madalena / Sousa, Cátia / Rufino, Ana T / Judas, Fernando / Mendes, Alexandrina F

    Journal of cellular physiology

    2020  Volume 235, Issue 11, Page(s) 8486–8494

    Abstract: Estrogen hormones are important for cartilage homeostasis, but nothing is known regarding the expression and role of the membrane G protein-coupled estrogen receptor (GPER), G protein-coupled receptor 30 (GPR30), in adult articular chondrocytes. Using ... ...

    Abstract Estrogen hormones are important for cartilage homeostasis, but nothing is known regarding the expression and role of the membrane G protein-coupled estrogen receptor (GPER), G protein-coupled receptor 30 (GPR30), in adult articular chondrocytes. Using immunohistochemistry of cartilage sections, quantitative real-time polymerase chain reaction and Western blot of chondrocyte extracts, we found that these cells express GPR30. Nonetheless, the pattern of bands detected by two distinct antibodies does not overlap, suggesting that the proteins detected represent partially degraded forms of the receptor. Treatment with GPR30 agonists did not induce Akt or ERK1/2 phosphorylation, two known GPR30-activated signaling pathways, suggesting that GPR30 is not functional in human chondrocytes. Therefore, the protective anti-osteoarthritic role of estrogen hormones in cartilage homeostasis is likely independent of GPR30. This study was performed using human cartilage collected from the distal femoral condyles of multiorgan donors at the Bone and Tissue Bank of the University and Hospital Center of Coimbra.
    MeSH term(s) Cartilage/metabolism ; Chondrocytes/metabolism ; Estrogen Receptor alpha/metabolism ; Estrogens/metabolism ; Humans ; Mitogen-Activated Protein Kinase 3 ; Receptors, Estrogen/metabolism ; Receptors, G-Protein-Coupled/metabolism ; Signal Transduction/drug effects
    Chemical Substances Estrogen Receptor alpha ; Estrogens ; GPER1 protein, human ; Receptors, Estrogen ; Receptors, G-Protein-Coupled ; MAPK3 protein, human (EC 2.7.11.24) ; Mitogen-Activated Protein Kinase 3 (EC 2.7.11.24)
    Keywords covid19
    Language English
    Publishing date 2020-04-23
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 3116-1
    ISSN 1097-4652 ; 0021-9541
    ISSN (online) 1097-4652
    ISSN 0021-9541
    DOI 10.1002/jcp.29691
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Physiology and pathophysiology of musculoskeletal aging: current research trends and future priorities.

    Mobasheri, Ali / Mendes, Alexandrina F

    Frontiers in physiology

    2013  Volume 4, Page(s) 73

    Language English
    Publishing date 2013-04-09
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2564217-0
    ISSN 1664-042X
    ISSN 1664-042X
    DOI 10.3389/fphys.2013.00073
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Multi-layered electrospinning and electrospraying approach: Effect of polymeric supplements on chondrocyte suspension.

    Semitela, Ângela / Leal Pereira, Andreia / Sousa, Cátia / Mendes, Alexandrina F / Marques, Paula A A P / Completo, António

    Journal of biomaterials applications

    2021  Volume 36, Issue 9, Page(s) 1629–1640

    Abstract: Articular cartilage was expected to be one of the first tissues to be successfully engineered, but replicating the complex fibril architecture and the cellular distribution of the native cartilage has proven difficult. While electrospinning has been ... ...

    Abstract Articular cartilage was expected to be one of the first tissues to be successfully engineered, but replicating the complex fibril architecture and the cellular distribution of the native cartilage has proven difficult. While electrospinning has been widely used to reproduce the depth-dependent fibre architecture in 3D scaffolds, the chondrocyte-controlled distribution remains an unsolved problem. To incorporate cells homogeneously through the depth of scaffolds, a combination of polymer electrospinning and cell seeding is necessary. A multi-layer approach alternating between polymer electrospinning with chondrocyte electrospraying can be a solution. Still, the success of this process is related to the survival rate of the electrosprayed chondrocytes embedded within the electrospun mesh. In this regard, the present study investigated the impact of the multi-layered process and the supplementation of the electrospray chondrocyte suspension with different concentrations of Gelatin and Alginate on the viability of electrosprayed chondrocytes embedded within a Polycaprolactone/Gelatin electrospun mesh and on the mechanical properties of the resulting meshes. The addition of Gelatin in the chondrocyte suspension did not increase significantly (
    MeSH term(s) Alginates ; Cartilage, Articular ; Chondrocytes ; Dietary Supplements ; Gelatin ; Polymers ; Tissue Engineering/methods ; Tissue Scaffolds
    Chemical Substances Alginates ; Polymers ; Gelatin (9000-70-8)
    Language English
    Publishing date 2021-12-31
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 639283-0
    ISSN 1530-8022 ; 0885-3282
    ISSN (online) 1530-8022
    ISSN 0885-3282
    DOI 10.1177/08853282211064403
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Dichotomous Sirtuins: Implications for Drug Discovery in Neurodegenerative and Cardiometabolic Diseases.

    Gomes, Pedro / Leal, Helena / Mendes, Alexandrina F / Reis, Flávio / Cavadas, Cláudia

    Trends in pharmacological sciences

    2019  Volume 40, Issue 12, Page(s) 1021–1039

    Abstract: Sirtuins (SIRT1-7), a class of ... ...

    Abstract Sirtuins (SIRT1-7), a class of NAD
    MeSH term(s) Animals ; Cardiovascular Diseases/drug therapy ; Cardiovascular Diseases/metabolism ; Drug Discovery ; Humans ; Metabolic Diseases/drug therapy ; Metabolic Diseases/metabolism ; Molecular Targeted Therapy ; Neurodegenerative Diseases/drug therapy ; Neurodegenerative Diseases/metabolism ; Sirtuins/antagonists & inhibitors ; Sirtuins/metabolism
    Chemical Substances Sirtuins (EC 3.5.1.-)
    Language English
    Publishing date 2019-11-06
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 282846-7
    ISSN 1873-3735 ; 0165-6147
    ISSN (online) 1873-3735
    ISSN 0165-6147
    DOI 10.1016/j.tips.2019.09.003
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Resveratrol modulates cytokine-induced Jak/STAT activation more efficiently than 5-aminosalicylic acid: an in vitro approach.

    Serra, Diana / Rufino, Ana T / Mendes, Alexandrina F / Almeida, Leonor M / Dinis, Teresa C P

    PloS one

    2014  Volume 9, Issue 10, Page(s) e109048

    Abstract: Background: Many advances have been recently made focused on the valuable help of dietary polyphenols in chronic inflammatory diseases. On the other hand, current treatment options for intestinal bowel disease patients are unsatisfying and, for this ... ...

    Abstract Background: Many advances have been recently made focused on the valuable help of dietary polyphenols in chronic inflammatory diseases. On the other hand, current treatment options for intestinal bowel disease patients are unsatisfying and, for this reason, it is estimated that many patients use dietary supplements to achieve extra benefits.
    Aim: The aim of this work was to analyze under a mechanistic perspective the anti-inflammatory potential of resveratrol, a natural polyphenolic compound, and to compare it with a pharmaceutical agent, 5-aminosalicylic acid, using the intestinal HT-29 cell line, as a cellular model.
    Methodology and principal findings: In the present study, HT-29 colon epithelial cells were pre-treated with 25 µM resveratrol and/or 500 µM 5-aminosalicylic acid and then exposed to a combination of cytokines (IL-1α, TNF-α, IFN-γ) for a certain period of time. Our data showed that resveratrol, used in a concentration 20 times lower than 5-aminosalicylic acid, was able to significantly reduce NO and PGE2 production, iNOS and COX-2 expression and reactive oxidant species formation induced by the cytokine challenge. However, as already verified with 5-aminosalicylic acid, in spite of not exhibiting any effect on IkB-α degradation, resveratrol down-regulated JAK-STAT pathway, decreasing the levels of activated STAT1 in the nucleus. Additionally, resveratrol decreased the cytokine-stimulated activation of SAPK/JNK pathway but did not counteract the cytokine-triggered negative feedback mechanism of STAT1, through p38 MAPK.
    Conclusion/significance: Taken together, our results show that resveratrol may be considered a future nutraceutical approach, promoting remission periods, limiting the inflammatory process and preventing colorectal cancer, which is common in these patients.
    MeSH term(s) Cytokines/physiology ; HT29 Cells ; Humans ; In Vitro Techniques ; Janus Kinases/metabolism ; Mesalamine/pharmacology ; Resveratrol ; STAT Transcription Factors/metabolism ; Stilbenes/pharmacology
    Chemical Substances Cytokines ; STAT Transcription Factors ; Stilbenes ; Mesalamine (4Q81I59GXC) ; Janus Kinases (EC 2.7.10.2) ; Resveratrol (Q369O8926L)
    Language English
    Publishing date 2014-10-01
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0109048
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  7. Article ; Online: Expression and function of K(ATP) channels in normal and osteoarthritic human chondrocytes: possible role in glucose sensing.

    Rufino, Ana T / Rosa, Susana C / Judas, Fernando / Mobasheri, Ali / Lopes, M Celeste / Mendes, Alexandrina F

    Journal of cellular biochemistry

    2013  Volume 114, Issue 8, Page(s) 1879–1889

    Abstract: ATP-sensitive potassium [K(ATP)] channels sense intracellular ATP/ADP levels, being essential components of a glucose-sensing apparatus in various cells that couples glucose metabolism, intracellular ATP/ADP levels and membrane potential. These channels ... ...

    Abstract ATP-sensitive potassium [K(ATP)] channels sense intracellular ATP/ADP levels, being essential components of a glucose-sensing apparatus in various cells that couples glucose metabolism, intracellular ATP/ADP levels and membrane potential. These channels are present in human chondrocytes, but their subunit composition and functions are unknown. This study aimed at elucidating the subunit composition of K(ATP) channels expressed in human chondrocytes and determining whether they play a role in regulating the abundance of major glucose transporters, GLUT-1 and GLUT-3, and glucose transport capacity. The results obtained show that human chondrocytes express the pore forming subunits, Kir6.1 and Kir6.2, at the mRNA and protein levels and the regulatory sulfonylurea receptor (SUR) subunits, SUR2A and SUR2B, but not SUR1. The expression of these subunits was no affected by culture under hyperglycemia-like conditions. Functional impairment of the channel activity, using a SUR blocker (glibenclamide 10 or 20 nM), reduced the protein levels of GLUT-1 and GLUT-3 by approximately 30% in normal chondrocytes, while in cells from cartilage with increasing osteoarthritic (OA) grade no changes were observed. Glucose transport capacity, however, was not affected in normal or OA chondrocytes. These results show that K(ATP) channel activity regulates the abundance of GLUT-1 and GLUT-3, although other mechanisms are involved in regulating the overall glucose transport capacity of human chondrocytes. Therefore, K(ATP) channels are potential components of a broad glucose sensing apparatus that modulates glucose transporters and allows human chondrocytes to adjust to varying extracellular glucose concentrations. This function of K(ATP) channels seems to be impaired in OA chondrocytes.
    MeSH term(s) Adult ; Aged ; Cells, Cultured ; Chondrocytes/enzymology ; Chondrocytes/pathology ; Female ; Glucose/metabolism ; Glucose Transporter Type 1/metabolism ; Glucose Transporter Type 3/metabolism ; Glyburide/pharmacology ; Humans ; Hypoglycemic Agents/pharmacology ; KATP Channels/metabolism ; Male ; Middle Aged ; Osteoarthritis/enzymology ; Osteoarthritis/pathology ; Potassium Channels, Inwardly Rectifying/metabolism
    Chemical Substances Glucose Transporter Type 1 ; Glucose Transporter Type 3 ; Hypoglycemic Agents ; KATP Channels ; Potassium Channels, Inwardly Rectifying ; SLC2A1 protein, human ; SLC2A3 protein, human ; Glucose (IY9XDZ35W2) ; Glyburide (SX6K58TVWC)
    Language English
    Publishing date 2013-03-15
    Publishing country United States
    Document type Clinical Trial ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 392402-6
    ISSN 1097-4644 ; 0730-2312
    ISSN (online) 1097-4644
    ISSN 0730-2312
    DOI 10.1002/jcb.24532
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  8. Article ; Online: Differential effects of the essential oils of Lavandula luisieri and Eryngium duriaei subsp. juresianum in cell models of two chronic inflammatory diseases.

    Rufino, Ana T / Ferreira, Isabel / Judas, Fernando / Salgueiro, Lígia / Lopes, M Celeste / Cavaleiro, Carlos / Mendes, Alexandrina F

    Pharmaceutical biology

    2015  Volume 53, Issue 8, Page(s) 1220–1230

    Abstract: Context: Effective drugs to treat osteoarthritis (OA) and inflammatory bowel disease (IBD) are needed.: Objective: To identify essential oils (EOs) with anti-inflammatory activity in cell models of OA and IBD.: Materials and methods: EOs from ... ...

    Abstract Context: Effective drugs to treat osteoarthritis (OA) and inflammatory bowel disease (IBD) are needed.
    Objective: To identify essential oils (EOs) with anti-inflammatory activity in cell models of OA and IBD.
    Materials and methods: EOs from Eryngium duriaei subsp. juresianum (M. Laínz) M. Laínz (Apiaceae), Laserpitium eliasii subsp. thalictrifolium Sennen & Pau (Apiaceae), Lavandula luisieri (Rozeira) Rivas-Martínez (Lamiaceae), Othantus maritimus (L.) Hoff. & Link (Asteraceae), and Thapsia villosa L. (Apiaceae) were analyzed by GC and GC/MS. The anti-inflammatory activity of EOs (5-200 μg/mL) was evaluated by measuring inducible nitric oxide synthase (iNOS) and nuclear factor-κB (NF-κB) activation (total and phosphorylated IκB-α), in primary human chondrocytes and the intestinal cell line, C2BBe1, stimulated with interleukin-1β (IL-1β) or interferon-γ (IFN-γ), IL-1β and tumor necrosis factor-α (TNF-α), respectively.
    Results: The EO of L. luisieri significantly reduced iNOS (by 54.9 and 81.0%, respectively) and phosphorylated IκB-α (by 87.4% and 62.3%, respectively) in both cell models. The EO of E. duriaei subsp. juresianum caused similar effects in human chondrocytes, but was inactive in intestinal cells, even at higher concentrations. The EOs of L. eliasii subsp. thalictrifolium and O. maritimus decreased iNOS expression by 45.2 ± 8.7% and 45.2 ± 6.2%, respectively, in C2BBe1 cells and were inactive in chondrocytes. The EO of T. villosa was inactive in both cell types.
    Discussion and conclusion: This is the first study showing anti-inflammatory effects of the EOs of L. luisieri and E. duriaei subsp. juresianum. These effects are specific of the cell type and may be valuable to develop new therapies or as sources of active compounds with improved efficacy and selectivity towards OA and IBD.
    MeSH term(s) Adult ; Aged ; Anti-Inflammatory Agents/isolation & purification ; Anti-Inflammatory Agents/pharmacology ; Anti-Inflammatory Agents/therapeutic use ; Cell Survival/drug effects ; Cell Survival/physiology ; Cells, Cultured ; Chondrocytes/drug effects ; Chondrocytes/metabolism ; Chondrocytes/pathology ; Chronic Disease ; Dose-Response Relationship, Drug ; Eryngium ; Female ; Humans ; Inflammation/drug therapy ; Inflammation/metabolism ; Inflammation/pathology ; Lavandula ; Male ; Middle Aged ; Oils, Volatile/isolation & purification ; Oils, Volatile/pharmacology ; Oils, Volatile/therapeutic use ; Plant Components, Aerial ; Plant Oils/isolation & purification ; Plant Oils/pharmacology ; Plant Oils/therapeutic use ; Treatment Outcome ; Young Adult
    Chemical Substances Anti-Inflammatory Agents ; Oils, Volatile ; Plant Oils
    Language English
    Publishing date 2015-08
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1440131-9
    ISSN 1744-5116 ; 1388-0209
    ISSN (online) 1744-5116
    ISSN 1388-0209
    DOI 10.3109/13880209.2014.970701
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Anti-inflammatory and chondroprotective activity of (+)-α-pinene: structural and enantiomeric selectivity.

    Rufino, Ana T / Ribeiro, Madalena / Judas, Fernando / Salgueiro, Lígia / Lopes, Maria C / Cavaleiro, Carlos / Mendes, Alexandrina F

    Journal of natural products

    2014  Volume 77, Issue 2, Page(s) 264–269

    Abstract: Previous studies have suggested that α-pinene, a common volatile plant metabolite, may have anti-inflammatory effects in human chondrocytes, thus exhibiting potential antiosteoarthritic activity. The objective of this study was to further characterize ... ...

    Abstract Previous studies have suggested that α-pinene, a common volatile plant metabolite, may have anti-inflammatory effects in human chondrocytes, thus exhibiting potential antiosteoarthritic activity. The objective of this study was to further characterize the potential antiosteoarthritic activity of selected pinene derivatives by evaluating their ability to modulate inflammation and extracellular matrix remodeling in human chondrocytes and to correlate the biological and chemical properties by determining whether the effects are isomer- and/or enantiomer-selective. To further elucidate chemicopharmacological interactions, the activities of other naturally occurring monoterpenes with the pinane nucleus were also investigated. At noncytotoxic concentrations, (+)-α-pinene (1) elicited the most potent inhibition of the IL-1β-induced inflammatory and catabolic pathways, namely, NF-κB and JNK activation and the expression of the inflammatory (iNOS) and catabolic (MMP-1 and -13) genes. (-)-α-Pinene (2) was less active than the (+)-enantiomer (1), and β-pinene (3) was inactive. E-Pinane (4) and oxygenated pinane-derived compounds, pinocarveol (5), myrtenal (6), (E)-myrtanol (7), myrtenol (8), and (Z)-verbenol (9), were less effective or even completely inactive and more cytotoxic than the pinenes tested (1-3). The data obtained show isomer- and enantiomer-selective anti-inflammatory and anticatabolic effects of α-pinene in human chondrocytes, (+)-α-pinene (1) being the most promising for further studies to determine its potential value as an antiosteoarthritic drug.
    MeSH term(s) Anti-Inflammatory Agents/chemistry ; Anti-Inflammatory Agents/pharmacology ; Chondrocytes/drug effects ; Humans ; Interleukin-1beta/metabolism ; MAP Kinase Kinase 4/drug effects ; Molecular Structure ; Monoterpenes/chemistry ; Monoterpenes/pharmacology ; NF-kappa B/antagonists & inhibitors ; Nitric Oxide Synthase Type II/drug effects ; Osteoarthritis/drug therapy ; Stereoisomerism ; Terpenes/pharmacology
    Chemical Substances Anti-Inflammatory Agents ; Interleukin-1beta ; Monoterpenes ; NF-kappa B ; Terpenes ; myrtenal (8J97443QRZ) ; Nitric Oxide Synthase Type II (EC 1.14.13.39) ; MAP Kinase Kinase 4 (EC 2.7.12.2) ; verbenol (G0F32F922S) ; alpha-pinene (JPF3YI7O34)
    Language English
    Publishing date 2014-02-28
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 304325-3
    ISSN 1520-6025 ; 0163-3864
    ISSN (online) 1520-6025
    ISSN 0163-3864
    DOI 10.1021/np400828x
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  10. Article: Anti-inflammatory and Chondroprotective Activity of (+)-α-Pinene: Structural and Enantiomeric Selectivity

    Rufino, Ana T / Ribeiro Madalena / Judas Fernando / Salgueiro Lígia / Lopes Maria C / Cavaleiro Carlos / Mendes Alexandrina F

    Journal of natural products. 2014 Feb. 28, v. 77, no. 2

    2014  

    Abstract: Previous studies have suggested that α-pinene, a common volatile plant metabolite, may have anti-inflammatory effects in human chondrocytes, thus exhibiting potential antiosteoarthritic activity. The objective of this study was to further characterize ... ...

    Abstract Previous studies have suggested that α-pinene, a common volatile plant metabolite, may have anti-inflammatory effects in human chondrocytes, thus exhibiting potential antiosteoarthritic activity. The objective of this study was to further characterize the potential antiosteoarthritic activity of selected pinene derivatives by evaluating their ability to modulate inflammation and extracellular matrix remodeling in human chondrocytes and to correlate the biological and chemical properties by determining whether the effects are isomer- and/or enantiomer-selective. To further elucidate chemicopharmacological interactions, the activities of other naturally occurring monoterpenes with the pinane nucleus were also investigated. At noncytotoxic concentrations, (+)-α-pinene (1) elicited the most potent inhibition of the IL-1β-induced inflammatory and catabolic pathways, namely, NF-κB and JNK activation and the expression of the inflammatory (iNOS) and catabolic (MMP-1 and -13) genes. (−)-α-Pinene (2) was less active than the (+)-enantiomer (1), and β-pinene (3) was inactive. E-Pinane (4) and oxygenated pinane-derived compounds, pinocarveol (5), myrtenal (6), (E)-myrtanol (7), myrtenol (8), and (Z)-verbenol (9), were less effective or even completely inactive and more cytotoxic than the pinenes tested (1–3). The data obtained show isomer- and enantiomer-selective anti-inflammatory and anticatabolic effects of α-pinene in human chondrocytes, (+)-α-pinene (1) being the most promising for further studies to determine its potential value as an antiosteoarthritic drug.
    Keywords alpha-pinene ; anti-inflammatory activity ; beta-pinene ; chondrocytes ; cytotoxicity ; drugs ; extracellular matrix ; genes ; humans ; inducible nitric oxide synthase ; inflammation ; metabolites ; mitogen-activated protein kinase ; physicochemical properties ; transcription factor NF-kappa B
    Language English
    Dates of publication 2014-0228
    Size p. 264-269.
    Publishing place American Chemical Society and American Society of Pharmacognosy
    Document type Article
    ZDB-ID 304325-3
    ISSN 1520-6025 ; 0163-3864
    ISSN (online) 1520-6025
    ISSN 0163-3864
    DOI 10.1021%2Fnp400828x
    Database NAL-Catalogue (AGRICOLA)

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