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  1. Artikel ; Online: Dietary Fatty Acid Saturation Modulates Sphingosine-1-Phosphate-Mediated Vascular Function.

    Nuno, Daniel W / Lamping, Kathryn G

    Journal of diabetes research

    2019  Band 2019, Seite(n) 2354274

    Abstract: Sphingolipids, modified by dietary fatty acids, are integral components of plasma membrane and caveolae that are also vasoactive compounds. We hypothesized that dietary fatty acid saturation affects vasoconstriction to sphingosine-1-phosphate (S1P) ... ...

    Abstract Sphingolipids, modified by dietary fatty acids, are integral components of plasma membrane and caveolae that are also vasoactive compounds. We hypothesized that dietary fatty acid saturation affects vasoconstriction to sphingosine-1-phosphate (S1P) through caveolar regulation of rho kinase. Wild type (WT) and caveolin-1-deficient (cav-1 KO) mice which lack vascular caveolae were fed a low-fat diet (LF), 60% high-saturated fat diet (lard, HF), or 60% fat diet with equal amounts of lard and n-3 polyunsaturated menhaden oil (MO). Weight gain of WT on HF and MO diets was similar while markedly blunted in cav-1 KO. Neither high-fat diet affected the expression of cav-1, rho, or rho kinase in arteries from WT. In cav-1 KO, MO increased the vascular expression of rho but had no effect on rho kinase. HF had no effect on rho or rho kinase expression in cav-1 KO. S1P produced a concentration-dependent constriction of gracilis arteries from WT on LF that was reduced with HF and restored to normal with MO. Constriction to S1P was reduced in cav-1 KO and no longer affected by a high-saturated fat diet. Inhibition of rho kinase which reduced constriction to PE independent of diet in arteries from WT and cav-1 KO only reduced constriction to S1P in arteries from WT fed MO. The data suggest that dietary fatty acids modify vascular responses to S1P by a caveolar-dependent mechanism which is enhanced by dietary n-3 polyunsaturated fats.
    Mesh-Begriff(e) Animals ; Arteries/metabolism ; Caveolin 1/genetics ; Caveolin 1/metabolism ; Diet, Fat-Restricted ; Diet, High-Fat ; Lysophospholipids/metabolism ; Mice ; Mice, Knockout ; Sphingosine/analogs & derivatives ; Sphingosine/metabolism ; rho-Associated Kinases/metabolism
    Chemische Substanzen Caveolin 1 ; Lysophospholipids ; sphingosine 1-phosphate (26993-30-6) ; rho-Associated Kinases (EC 2.7.11.1) ; Sphingosine (NGZ37HRE42)
    Sprache Englisch
    Erscheinungsdatum 2019-08-25
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 2711897-6
    ISSN 2314-6753 ; 2314-6745
    ISSN (online) 2314-6753
    ISSN 2314-6745
    DOI 10.1155/2019/2354274
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Sex-Specific Differences in Endothelial Function Are Driven by Divergent Mitochondrial Ca

    Damacena de Angelis, Celio / Endoni, Benney T / Nuno, Daniel / Lamping, Kathryn / Ledolter, Johannes / Koval, Olha M / Grumbach, Isabella M

    Journal of the American Heart Association

    2022  Band 11, Heft 13, Seite(n) e023912

    Abstract: Background Sex-specific differences in vasodilation are mediated in part by differences in cytosolic ... ...

    Abstract Background Sex-specific differences in vasodilation are mediated in part by differences in cytosolic Ca
    Mesh-Begriff(e) Animals ; Calcium/metabolism ; Calcium Channels/genetics ; Calcium Channels/metabolism ; Endothelial Cells/metabolism ; Estradiol/pharmacology ; Female ; Humans ; Male ; Mice ; Mitochondria/metabolism ; Sex Characteristics
    Chemische Substanzen Calcium Channels ; Estradiol (4TI98Z838E) ; Calcium (SY7Q814VUP)
    Sprache Englisch
    Erscheinungsdatum 2022-06-29
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2653953-6
    ISSN 2047-9980 ; 2047-9980
    ISSN (online) 2047-9980
    ISSN 2047-9980
    DOI 10.1161/JAHA.121.023912
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Endothelial progenitor cells: sowing the seeds for vascular repair.

    Lamping, Kathryn

    Circulation research

    2007  Band 100, Heft 9, Seite(n) 1243–1245

    Mesh-Begriff(e) Animals ; Cyclooxygenase 2/biosynthesis ; Endothelial Cells/cytology ; Epoprostenol/biosynthesis ; Humans ; Nitric Oxide/physiology ; Regeneration ; Stem Cell Transplantation ; Stem Cells/physiology ; Vascular Diseases/therapy
    Chemische Substanzen Nitric Oxide (31C4KY9ESH) ; Epoprostenol (DCR9Z582X0) ; Cyclooxygenase 2 (EC 1.14.99.1)
    Sprache Englisch
    Erscheinungsdatum 2007-05-11
    Erscheinungsland United States
    Dokumenttyp Comment ; Editorial ; Research Support, Non-U.S. Gov't
    ZDB-ID 80100-8
    ISSN 1524-4571 ; 0009-7330 ; 0931-6876
    ISSN (online) 1524-4571
    ISSN 0009-7330 ; 0931-6876
    DOI 10.1161/01.RES.0000268193.46418.d1
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Dietary fats modify vascular fat composition, eNOS localization within lipid rafts and vascular function in obesity.

    Nuno, Daniel W / Coppey, Lawrence J / Yorek, Mark A / Lamping, Kathryn G

    Physiological reports

    2018  Band 6, Heft 15, Seite(n) e13820

    Abstract: We tested whether dietary fatty acids alter membrane composition shifting localization of signaling pathways within caveolae to determine their role in vascular function. Wild type (WT) and caveolin-1-deficient mice (cav-1 KO), required for vascular ... ...

    Abstract We tested whether dietary fatty acids alter membrane composition shifting localization of signaling pathways within caveolae to determine their role in vascular function. Wild type (WT) and caveolin-1-deficient mice (cav-1 KO), required for vascular caveolae formation, were fed low fat (LF), high saturated fat (HF, 60% kcal from lard), or high-fat diet with 50:50 lard and n-3 polyunsaturated fatty acid-enriched menhaden oil (MO). HF and MO increased body weight and fat in WT but had less effect in cav-1 KO. MO increased unsaturated fatty acids and the unsaturation index of aorta from WT and cav-1 KO. In LF WT aorta, endothelial nitric oxide synthase (eNOS) was localized to cav-1-enriched low-density fractions which shifted to actin-enriched high-density fractions with acetylcholine (ACh). HF and MO shifted eNOS to high-density fractions in WT aorta which was not affected by ACh. In cav-1 KO aorta, eNOS was localized in low-density non-caveolar fractions but not shifted by ACh or diet. Inducible NOS and cyclooxygenase 1/2 were not localized in low-density fractions or affected by diet, ACh or genotype. ACh-induced dilation of gracilis arteries from HF WT was similar to dilation in LF but the NOS component was reduced. In WT and cav-1 KO, dilation to ACh was enhanced by MO through increased role for NOS and cyclooxygenase. We conclude that dietary fats affect vascular fatty acid composition and membrane localization of eNOS but the contribution of eNOS and cyclooxygenase in ACh-mediated vascular responses is independent of lipid rafts.
    Mesh-Begriff(e) Acetylcholine/pharmacology ; Animals ; Aorta/drug effects ; Aorta/metabolism ; Blood Glucose/metabolism ; Body Composition/drug effects ; Body Composition/physiology ; Body Weight/drug effects ; Body Weight/physiology ; Caveolae/metabolism ; Caveolin 1/deficiency ; Caveolin 1/physiology ; Diet, High-Fat ; Dietary Fats/administration & dosage ; Dietary Fats/pharmacology ; Fatty Acids/metabolism ; Fish Oils/pharmacology ; Gracilis Muscle/blood supply ; Male ; Mice, Inbred C57BL ; Mice, Knockout ; Nitric Oxide Synthase Type III/metabolism ; Obesity/metabolism ; Obesity/physiopathology ; Vasodilation/drug effects ; Vasodilation/physiology
    Chemische Substanzen Blood Glucose ; Caveolin 1 ; Dietary Fats ; Fatty Acids ; Fish Oils ; Menhaden oil (1D8HWC57D0) ; Nitric Oxide Synthase Type III (EC 1.14.13.39) ; Acetylcholine (N9YNS0M02X)
    Sprache Englisch
    Erscheinungsdatum 2018-07-11
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2724325-4
    ISSN 2051-817X ; 2051-817X
    ISSN (online) 2051-817X
    ISSN 2051-817X
    DOI 10.14814/phy2.13820
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: The role of rho kinase in sex-dependent vascular dysfunction in type 1 diabetes.

    Nuno, Daniel W / Lamping, Kathryn G

    Experimental diabetes research

    2010  Band 2010, Seite(n) 176361

    Abstract: We hypothesized that rho/rho kinase plays a role in sex differences in vascular dysfunction of diabetics. Contractions to serotonin were greater in isolated aortic rings from nondiabetic males versus females and increased further in streptozotocin- ... ...

    Abstract We hypothesized that rho/rho kinase plays a role in sex differences in vascular dysfunction of diabetics. Contractions to serotonin were greater in isolated aortic rings from nondiabetic males versus females and increased further in streptozotocin-induced diabetic males but not females. The increased contractions to serotonin in males were reduced by inhibitors of rho kinase (fasudil, Y27632 and H1152) despite no change in expression of rhoA or rho kinase. Contractions to U46619 were not altered by fasudil or Y27632 or the presence of diabetes. In contrast to acute effects of fasudil, chronic treatment with fasudil increased contractions to serotonin in aorta from both non-diabetic and diabetic males. In summary, serotonin-induced contractions were increased in aorta from diabetic males but not females. Although administration of rho kinase inhibitors acutely decreased contractions to serotonin, long-term treatment with fasudil increased contractions. Long-term fasudil treatment may increase compensatory mechanisms to enhance vasoconstrictions.
    Mesh-Begriff(e) 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/analogs & derivatives ; 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/pharmacology ; Animals ; Diabetes Mellitus, Experimental/physiopathology ; Diabetes Mellitus, Type 1/physiopathology ; Diabetic Angiopathies/etiology ; Female ; Male ; Mice ; Mice, Inbred BALB C ; Sex Characteristics ; Streptozocin ; Vasoconstriction/drug effects ; Vasodilation/drug effects ; rho-Associated Kinases/physiology ; rhoA GTP-Binding Protein/physiology
    Chemische Substanzen Streptozocin (5W494URQ81) ; 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine (84477-87-2) ; rho-Associated Kinases (EC 2.7.11.1) ; rhoA GTP-Binding Protein (EC 3.6.5.2) ; fasudil (Q0CH43PGXS)
    Sprache Englisch
    Erscheinungsdatum 2010-03-24
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2465179-5
    ISSN 1687-5303 ; 1687-5214
    ISSN (online) 1687-5303
    ISSN 1687-5214
    DOI 10.1155/2010/176361
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Enhanced contractile mechanisms in vasospasm: is endothelial dysfunction the whole story?

    Lamping, Kathryn G

    Circulation

    2002  Band 105, Heft 13, Seite(n) 1520–1522

    Mesh-Begriff(e) 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/analogs & derivatives ; 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/pharmacology ; Animals ; Calcium/metabolism ; Coronary Vasospasm/enzymology ; Coronary Vasospasm/physiopathology ; Coronary Vasospasm/prevention & control ; Endothelium, Vascular/physiopathology ; Enzyme Inhibitors/pharmacology ; Humans ; Intracellular Signaling Peptides and Proteins ; Muscle Contraction ; Muscle, Smooth, Vascular/physiopathology ; Nitric Oxide/physiology ; Protein-Serine-Threonine Kinases/antagonists & inhibitors ; Swine ; Vasoconstriction ; rho-Associated Kinases ; rhoA GTP-Binding Protein/physiology
    Chemische Substanzen Enzyme Inhibitors ; Intracellular Signaling Peptides and Proteins ; Nitric Oxide (31C4KY9ESH) ; 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine (84477-87-2) ; Protein-Serine-Threonine Kinases (EC 2.7.11.1) ; rho-Associated Kinases (EC 2.7.11.1) ; rhoA GTP-Binding Protein (EC 3.6.5.2) ; fasudil (Q0CH43PGXS) ; Calcium (SY7Q814VUP)
    Sprache Englisch
    Erscheinungsdatum 2002-04-02
    Erscheinungsland United States
    Dokumenttyp Editorial ; Comment
    ZDB-ID 80099-5
    ISSN 1524-4539 ; 0009-7322 ; 0069-4193 ; 0065-8499
    ISSN (online) 1524-4539
    ISSN 0009-7322 ; 0069-4193 ; 0065-8499
    DOI 10.1161/01.cir.0000014120.90086.51
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: N-Heterocyclic Carbene-Modified Au-Pd Alloy Nanoparticles and Their Application as Biomimetic and Heterogeneous Catalysts.

    Tegeder, Patricia / Freitag, Matthias / Chepiga, Kathryn M / Muratsugu, Satoshi / Möller, Nadja / Lamping, Sebastian / Tada, Mizuki / Glorius, Frank / Ravoo, Bart Jan

    Chemistry (Weinheim an der Bergstrasse, Germany)

    2018  Band 24, Heft 70, Seite(n) 18682–18688

    Abstract: The preparation of water-soluble, N-heterocyclic-carbene-stabilized Au-Pd alloy nanoparticles by a straightforward ligand exchange process is presented. Extensive analysis revealed excellent size retention and stability over years in water. The alloy ... ...

    Abstract The preparation of water-soluble, N-heterocyclic-carbene-stabilized Au-Pd alloy nanoparticles by a straightforward ligand exchange process is presented. Extensive analysis revealed excellent size retention and stability over years in water. The alloy nanoparticles were applied as biomimetic catalysts for aerobic oxidation of d-glucose, for which monometallic Au and Pd nanoparticles showed no or negligible activity. The alloy nanoparticles were further applied as titania-supported heterogeneous catalysts for the mild hydrogenation of nitroarenes and the semihydrogenation of 1,2-diphenylacetylene with a solvent-dependent selectivity switch between E- and Z-stilbene.
    Mesh-Begriff(e) Alloys/chemistry ; Catalysis ; Glucose/chemistry ; Gold/chemistry ; Hydrogenation ; Methane/analogs & derivatives ; Methane/chemistry ; Nanoparticles/chemistry ; Oxidation-Reduction ; Palladium/chemistry ; Particle Size ; Stereoisomerism ; Stilbenes/chemistry ; Titanium/chemistry
    Chemische Substanzen Alloys ; Stilbenes ; titanium dioxide (15FIX9V2JP) ; carbene (2465-56-7) ; Palladium (5TWQ1V240M) ; Gold (7440-57-5) ; Titanium (D1JT611TNE) ; Glucose (IY9XDZ35W2) ; Methane (OP0UW79H66)
    Sprache Englisch
    Erscheinungsdatum 2018-11-12
    Erscheinungsland Germany
    Dokumenttyp Journal Article
    ZDB-ID 1478547-x
    ISSN 1521-3765 ; 0947-6539
    ISSN (online) 1521-3765
    ISSN 0947-6539
    DOI 10.1002/chem.201803274
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: Conceptualizing and measuring health-related quality of life in critical care.

    Lim, Wan Chin / Black, Nick / Lamping, Donna / Rowan, Kathryn / Mays, Nicholas

    Journal of critical care

    2016  Band 31, Heft 1, Seite(n) 183–193

    Abstract: Introduction: When assessing health-related quality of life (HRQL), critical care outcomes research generally uses generic measures in the absence of a suitable critical care-specific measure. Our aims were to construct a conceptual framework of ... ...

    Abstract Introduction: When assessing health-related quality of life (HRQL), critical care outcomes research generally uses generic measures in the absence of a suitable critical care-specific measure. Our aims were to construct a conceptual framework of survivors' HRQL and assess the extent to which the 2 most commonly used generic measures (the Short Form 36 Health Survey and EuroQol-5D) covered the framework.
    Methods: A preliminary framework for survivors' HRQL was constructed based on a systematic literature review and on a secondary analysis of 40 existing in-depth interviews with adult, critical care survivors. Its adequacy was then tested using new in-depth interviews with a maximum variation sample of critical care survivors. The extent of coverage of the final framework by the 2 generic HRQL instruments was then evaluated in 2 ways: by comparison with critical care survivors' accounts from the new in-depth interviews and by eliciting survivors' views on the adequacy of the 2 generic HRQL instruments using cognitive debriefing.
    Results: The final framework recognized 3 aspects of health status that affected 9 areas of life. The 2 most commonly used generic measures had substantial gaps in their coverage of the framework of survivors' HRQL.
    Conclusions: The findings argue strongly for a new critical care-specific HRQL measure.
    Mesh-Begriff(e) Activities of Daily Living ; Adult ; Aged ; Cognition ; Cohort Studies ; Critical Care/psychology ; Critical Illness/psychology ; Female ; Health Status ; Humans ; Interpersonal Relations ; Length of Stay ; Male ; Middle Aged ; Outcome Assessment (Health Care) ; Personality ; Qualitative Research ; Quality of Life/psychology ; Residence Characteristics ; Social Participation ; Survivors/psychology
    Sprache Englisch
    Erscheinungsdatum 2016-02
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 632818-0
    ISSN 1557-8615 ; 0883-9441
    ISSN (online) 1557-8615
    ISSN 0883-9441
    DOI 10.1016/j.jcrc.2015.10.020
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: RhoA localization with caveolin-1 regulates vascular contractions to serotonin.

    Nuno, Daniel W / England, Sarah K / Lamping, Kathryn G

    American journal of physiology. Regulatory, integrative and comparative physiology

    2012  Band 303, Heft 9, Seite(n) R959–67

    Abstract: Vascular smooth muscle contraction occurs following an initial response to an increase in intracellular calcium concentration and a sustained response following increases in the sensitivity of contractile proteins to calcium (calcium sensitization). This ...

    Abstract Vascular smooth muscle contraction occurs following an initial response to an increase in intracellular calcium concentration and a sustained response following increases in the sensitivity of contractile proteins to calcium (calcium sensitization). This latter process is regulated by the rhoA/rho kinase pathway and activated by serotonin. In multiple cell types, signaling molecules compartmentalize within caveolae to regulate their activation. We hypothesized that serotonin differentially compartmentalizes rhoA within caveolar versus noncaveolar lipid rafts to regulate sustained vascular contractions. To test this hypothesis, we measured aortic contractions in response to serotonin in wild-type (WT) and cav-1-deficient mice (cav-1 KO). RhoA-dependent contractions in response to serotonin were markedly augmented in arteries from cav-1 KO mice despite a modest reduction in rhoA expression compared with WT. We found that under basal conditions, rhoA in WT arteries was primarily localized within high-density sucrose gradient fractions but temporally shifted to low-density fractions in response to serotonin. In contrast, rhoA in cav-1 KO arteries was primarily in low-density fractions and shifted to high-density fractions in a similar timeframe as that seen in WT mice. We conclude that localization of rhoA to caveolar versus noncaveolar lipid rafts differentially regulates its activation and contractions to rhoA-dependent agonists with greater activation associated with its localization to noncaveolar rafts. Disruption of rhoA localization within caveolae may contribute to increased activation and enhanced vascular contractions in cardiovascular disease.
    Mesh-Begriff(e) Animals ; Aorta/cytology ; Aorta/metabolism ; Arteries/cytology ; Arteries/metabolism ; Caveolin 1/deficiency ; Caveolin 1/genetics ; Caveolin 1/metabolism ; Male ; Membrane Microdomains/metabolism ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Models, Animal ; Muscle Contraction/drug effects ; Muscle Contraction/physiology ; Muscle, Smooth, Vascular/cytology ; Muscle, Smooth, Vascular/metabolism ; Serotonin/pharmacology ; Signal Transduction/physiology ; Vasoconstriction/drug effects ; Vasoconstriction/physiology ; rho GTP-Binding Proteins/metabolism ; rho-Associated Kinases/metabolism ; rhoA GTP-Binding Protein
    Chemische Substanzen Caveolin 1 ; Serotonin (333DO1RDJY) ; rho-Associated Kinases (EC 2.7.11.1) ; RhoA protein, mouse (EC 3.6.5.2) ; rho GTP-Binding Proteins (EC 3.6.5.2) ; rhoA GTP-Binding Protein (EC 3.6.5.2)
    Sprache Englisch
    Erscheinungsdatum 2012-09-05
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 603839-6
    ISSN 1522-1490 ; 0363-6119
    ISSN (online) 1522-1490
    ISSN 0363-6119
    DOI 10.1152/ajpregu.00667.2011
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: 5HT(2A) and 5HT(2B) receptors contribute to serotonin-induced vascular dysfunction in diabetes.

    Nelson, Peter M / Harrod, Jeremy S / Lamping, Kathryn G

    Experimental diabetes research

    2012  Band 2012, Seite(n) 398406

    Abstract: Although 5HT(2A) receptors mediate contractions of normal arteries to serotonin (5HT), in some cardiovascular diseases, other receptor subtypes contribute to the marked increase in serotonin contractions. We hypothesized that enhanced contractions of ... ...

    Abstract Although 5HT(2A) receptors mediate contractions of normal arteries to serotonin (5HT), in some cardiovascular diseases, other receptor subtypes contribute to the marked increase in serotonin contractions. We hypothesized that enhanced contractions of arteries from diabetics to 5HT are mediated by an increased contribution from multiple 5HT receptor subtypes. We compared responses to selective 5HT receptor agonists and expression of 5HT receptor isoforms (5HT(1B), 5HT(2A), and 5HT(2B)) in aorta from nondiabetic (ND) compared to type 2 diabetic mice (DB, BKS.Cg-Dock7(m)+/+Lepr(db)/J). 5HT, 5HT(2A) (TCB2 and BRL54443), and 5HT(2B) (norfenfluramine and BW723C86) receptor agonists produced concentration-dependent contractions of ND arteries that were markedly increased in DB arteries. Neither ND nor DB arteries contracted to a 5HT(1B) receptor agonist. MDL11939, a 5HT(2A) receptor antagonist, and LY272015, a 5HT(2B) receptor antagonist, reduced contractions of arteries from DB to 5HT more than ND. Expression of 5HT(1B), 5HT(2A), and 5HT(2B) receptor subtypes was similar in ND and DB. Inhibition of rho kinase decreased contractions to 5HT and 5HT(2A) and 5HT(2B) receptor agonists in ND and DB. We conclude that in contrast to other cardiovascular diseases, enhanced contraction of arteries from diabetics to 5HT is not due to a change in expression of multiple 5HT receptor subtypes.
    Mesh-Begriff(e) Animals ; Aorta/drug effects ; Aorta/metabolism ; Aorta/physiopathology ; Diabetes Mellitus, Type 2/complications ; Diabetes Mellitus, Type 2/genetics ; Diabetes Mellitus, Type 2/metabolism ; Diabetes Mellitus, Type 2/physiopathology ; Diabetic Angiopathies/genetics ; Diabetic Angiopathies/metabolism ; Diabetic Angiopathies/physiopathology ; Disease Models, Animal ; Dose-Response Relationship, Drug ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Protein Kinase Inhibitors/pharmacology ; Receptor, Serotonin, 5-HT2A/deficiency ; Receptor, Serotonin, 5-HT2A/drug effects ; Receptor, Serotonin, 5-HT2A/genetics ; Receptor, Serotonin, 5-HT2A/metabolism ; Receptor, Serotonin, 5-HT2B/deficiency ; Receptor, Serotonin, 5-HT2B/drug effects ; Receptor, Serotonin, 5-HT2B/genetics ; Receptor, Serotonin, 5-HT2B/metabolism ; Serotonin/metabolism ; Serotonin 5-HT2 Receptor Agonists/pharmacology ; Serotonin 5-HT2 Receptor Antagonists/pharmacology ; Signal Transduction ; Vasoconstriction/drug effects ; Vasoconstrictor Agents/pharmacology ; rho-Associated Kinases/antagonists & inhibitors ; rho-Associated Kinases/metabolism
    Chemische Substanzen Protein Kinase Inhibitors ; Receptor, Serotonin, 5-HT2A ; Receptor, Serotonin, 5-HT2B ; Serotonin 5-HT2 Receptor Agonists ; Serotonin 5-HT2 Receptor Antagonists ; Vasoconstrictor Agents ; Serotonin (333DO1RDJY) ; rho-Associated Kinases (EC 2.7.11.1)
    Sprache Englisch
    Erscheinungsdatum 2012-12-30
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2465179-5
    ISSN 1687-5303 ; 1687-5214
    ISSN (online) 1687-5303
    ISSN 1687-5214
    DOI 10.1155/2012/398406
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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