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  1. Article ; Online: High-Salt Intake Reduces Apomorphine-Induced Penile Erection and Increases Neurally Mediated Contractile Responses of the Cavernosal Smooth Muscle in Rats.

    Leitolis, Amanda / Crestani, Sandra / Linder, Áurea Elizabeth / da Silva-Santos, José Eduardo

    American journal of hypertension

    2019  Volume 32, Issue 12, Page(s) 1206–1213

    Abstract: Background: This study was designed to evaluate whether overconsumption of NaCl, a well-known risk factor for hypertension, leads to erectile dysfunction in rodents.: Methods: Male Wistar rats received regular chow (control group) or 4% NaCl chow for ...

    Abstract Background: This study was designed to evaluate whether overconsumption of NaCl, a well-known risk factor for hypertension, leads to erectile dysfunction in rodents.
    Methods: Male Wistar rats received regular chow (control group) or 4% NaCl chow for 24 weeks and were subjected to blood pressure measurement and apomorphine-induced erection. Moreover, cavernosal strips from both the control and 4% NaCl groups were evaluated in organ baths.
    Results: Animals subjected to 4% NaCl chow did not develop hypertension but presented a significant reduction in the total number of erections following apomorphine administration as compared with the control group. The addition of high KCl or phenylephrine resulted in similar contractile responses in the corpus cavernosal strips from both the control and 4% NaCl groups. However, electrical field stimulation-induced contraction was significantly enhanced in cavernosal strips from animals exposed to 4% NaCl. Incubation of Y-27632, but not of atropine and Nω-nitro-l-arginine methyl ester (L-NAME), entirely prevented the potentiation of the contractile responses evoked by electrical stimulation. The enhanced contractile responses evoked by electrical stimulation found in the high-salt group were also avoided in the absence of extracellular calcium. Concentration-response curves of CaCl2 revealed augmented contractility in response to extracellular calcium in cavernosal strips from the 4% NaCl-treated rats, compared with control samples.
    Conclusions: A high-salt diet alone rendered the animals less responsive to apomorphine-induced penile erection and enhanced neurally mediated contractile responses in the corpus cavernosum, a clear indication that overconsumption of sodium can lead to erectile dysfunction even without the development of hypertension.
    MeSH term(s) Animals ; Apomorphine/pharmacology ; Calcium Signaling ; Electric Stimulation ; Erectile Dysfunction/etiology ; Erectile Dysfunction/metabolism ; Erectile Dysfunction/physiopathology ; Male ; Muscle Contraction/drug effects ; Muscle, Smooth/innervation ; Penile Erection/drug effects ; Penis/innervation ; Rats, Wistar ; Sodium Chloride, Dietary/toxicity ; rho-Associated Kinases/metabolism
    Chemical Substances Sodium Chloride, Dietary ; rho-Associated Kinases (EC 2.7.11.1) ; Apomorphine (N21FAR7B4S)
    Language English
    Publishing date 2019-09-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 639383-4
    ISSN 1941-7225 ; 1879-1905 ; 0895-7061
    ISSN (online) 1941-7225 ; 1879-1905
    ISSN 0895-7061
    DOI 10.1093/ajh/hpz142
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: High-Salt Intake Augments the Activity of the RhoA/ROCK Pathway and Reduces Intracellular Calcium in Arteries From Rats.

    Crestani, Sandra / Webb, Robert Clinton / da Silva-Santos, José Eduardo

    American journal of hypertension

    2017  Volume 30, Issue 4, Page(s) 389–399

    Abstract: Background: We investigated the influence of salt overconsumption on the functionality of the RhoA/Rho-associated kinase (ROCK) pathway and calcium regulation in arteries.: Methods: The aorta and small mesenteric arteries from rats fed a chow ... ...

    Abstract Background: We investigated the influence of salt overconsumption on the functionality of the RhoA/Rho-associated kinase (ROCK) pathway and calcium regulation in arteries.
    Methods: The aorta and small mesenteric arteries from rats fed a chow containing 2%, 4%, or 8% NaCl were evaluated in organ baths for the activity of the RhoA/ROCK pathway and intracellular calcium mobilization. Components of these pathways and intracellular calcium levels were also assessed in samples from 4% NaCl group.
    Results: In arteries from animals fed regular chow, the ROCK inhibitor Y-27632 reduced the responses to phenylephrine, even when the smallest concentrations (1 and 3 μM) were tested. However, only higher concentrations of Y-27632 (10 and 50 μM) reduced phenylephrine-induced contraction in vessels from high-salt groups. Immunoblotting revealed augmented phosphorylation of the myosin phosphatase targeting subunit 1 and increased amounts of RhoA in the membrane fraction of aorta homogenates from the 4% NaCl group. Under calcium-free solution, vessels from NaCl groups presented reduced contractile responses to phenylephrine and caffeine, compared with the regular chow group. Moreover, decreased intracellular calcium at rest and after stimulation with ATP were found in aortic smooth muscle cells from 4% NaCl-fed rats, which also showed diminished levels of SERCA2 and SERCA3, but not of IP3 and ryanodine receptors, or STIM1 and Orai1 proteins.
    Conclusions: Arteries from rats subjected to high-salt intake are unable to properly regulate intracellular calcium levels and present augmented activity of the calcium sensitization pathway RhoA/ROCK. These changes may precede the development of vascular diseases induced by high-salt intake.
    MeSH term(s) Amides/pharmacology ; Animals ; Aorta/cytology ; Aorta/drug effects ; Aorta/metabolism ; Calcium/metabolism ; Enzyme Inhibitors/pharmacology ; Inositol 1,4,5-Trisphosphate Receptors/drug effects ; Inositol 1,4,5-Trisphosphate Receptors/metabolism ; Male ; Mesenteric Arteries/cytology ; Mesenteric Arteries/drug effects ; Mesenteric Arteries/metabolism ; Myocytes, Smooth Muscle/drug effects ; Myocytes, Smooth Muscle/metabolism ; ORAI1 Protein/drug effects ; ORAI1 Protein/metabolism ; Phenylephrine/pharmacology ; Phosphorylation/drug effects ; Protein Phosphatase 1/drug effects ; Protein Phosphatase 1/metabolism ; Pyridines/pharmacology ; Rats ; Rats, Wistar ; Ryanodine Receptor Calcium Release Channel/drug effects ; Ryanodine Receptor Calcium Release Channel/metabolism ; Sarcoplasmic Reticulum Calcium-Transporting ATPases/drug effects ; Sarcoplasmic Reticulum Calcium-Transporting ATPases/metabolism ; Signal Transduction/drug effects ; Sodium Chloride, Dietary/pharmacology ; Stromal Interaction Molecule 1/drug effects ; Stromal Interaction Molecule 1/metabolism ; Vasoconstriction/drug effects ; Vasoconstrictor Agents/pharmacology ; rho GTP-Binding Proteins/drug effects ; rho GTP-Binding Proteins/metabolism ; rho-Associated Kinases/drug effects ; rho-Associated Kinases/metabolism
    Chemical Substances Amides ; Atp2a2 protein, rat ; Atp2a3 protein, rat ; Enzyme Inhibitors ; Inositol 1,4,5-Trisphosphate Receptors ; ORAI1 Protein ; Orai1 protein, rat ; Pyridines ; Ryanodine Receptor Calcium Release Channel ; Sodium Chloride, Dietary ; Stim1 protein, rat ; Stromal Interaction Molecule 1 ; Vasoconstrictor Agents ; Y 27632 (138381-45-0) ; Phenylephrine (1WS297W6MV) ; rho-Associated Kinases (EC 2.7.11.1) ; Ppp1r12a protein, rat (EC 3.1.3.16) ; Protein Phosphatase 1 (EC 3.1.3.16) ; Sarcoplasmic Reticulum Calcium-Transporting ATPases (EC 3.6.3.8) ; RhoA protein, rat (EC 3.6.5.2) ; rho GTP-Binding Proteins (EC 3.6.5.2) ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 2017-02-02
    Publishing country United States
    Document type Journal Article
    ZDB-ID 639383-4
    ISSN 1941-7225 ; 1879-1905 ; 0895-7061
    ISSN (online) 1941-7225 ; 1879-1905
    ISSN 0895-7061
    DOI 10.1093/ajh/hpw201
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Enhanced target-specific signal detection using an Escherichia coli lysate in multiplex microbead immunoassays with E. coli-derived recombinant antigens

    Crestani, Sandra / Amanda Leitolis / Leonardo Foti / Lucianna Freitas Oliveira Lima / Marco A. Krieger

    Journal of Immunological Methods. 2016 Aug., v. 435

    2016  

    Abstract: Diverse techniques have been developed to analyze antibody-mediated responses to infections. However, the most common tests, i.e., enzyme-linked immunosorbent assays, require separate reactions for each antigen and consequently necessitate large sample ... ...

    Abstract Diverse techniques have been developed to analyze antibody-mediated responses to infections. However, the most common tests, i.e., enzyme-linked immunosorbent assays, require separate reactions for each antigen and consequently necessitate large sample volumes. Luminex technology allows the detection of multiple antibodies in a single experiment, but nonspecific binding can impair the results. Therefore, we examined the use of Escherichia coli lysates to reduce nonspecific binding and improve the results of liquid microarrays based on Luminex technology. Anti-bacteria antibodies were detected in human serum samples, as evidenced by high median fluorescence intensity (MFI) in assays performed with paramagnetic microspheres coupled with E. coli lysates. Moreover, the addition of an E. coli lysate as a blocker reduced the nonspecific binding of antigens produced by E. coli in a concentration-dependent manner. Tris-HCl reduced MFI values in negative samples, but did not affect MFI for positive samples. For microspheres coupled with different antigens, an E. coli lysate blocker significantly improved the fluorescence signals from positive samples. The addition of Tris-HCl and the E. coli lysate induced antigen-specific differences in MFI. This combination of the E. coli lysate blocker and Tris-HCl yielded a statistically significant improvement in MFI in the assays for Chagas disease and hepatitis C virus samples. However, for the Treponema pallidum p47 antigen improvement in MFI was only observed for the preparation with the E. coli blocker at a concentration of 3%. In conclusion, the addition of an E. coli lysate and Tris-HCl to the microarray assay reduced the nonspecific binding of human anti-bacteria antibodies and, therefore, increased the specific MFI.
    Keywords antibodies ; blood serum ; Chagas disease ; enzyme-linked immunosorbent assay ; Escherichia coli ; fluorescence ; Hepatitis C virus ; humans ; microarray technology ; microbeads ; recombinant antigens ; Treponema pallidum
    Language English
    Dates of publication 2016-08
    Size p. 17-26.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 120142-6
    ISSN 1872-7905 ; 0022-1759
    ISSN (online) 1872-7905
    ISSN 0022-1759
    DOI 10.1016/j.jim.2016.05.002
    Database NAL-Catalogue (AGRICOLA)

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  4. Article ; Online: Enhanced target-specific signal detection using an Escherichia coli lysate in multiplex microbead immunoassays with E. coli-derived recombinant antigens.

    Crestani, Sandra / Leitolis, Amanda / Lima, Lucianna Freitas Oliveira / Krieger, Marco A / Foti, Leonardo

    Journal of immunological methods

    2016  Volume 435, Page(s) 17–26

    Abstract: Diverse techniques have been developed to analyze antibody-mediated responses to infections. However, the most common tests, i.e., enzyme-linked immunosorbent assays, require separate reactions for each antigen and consequently necessitate large sample ... ...

    Abstract Diverse techniques have been developed to analyze antibody-mediated responses to infections. However, the most common tests, i.e., enzyme-linked immunosorbent assays, require separate reactions for each antigen and consequently necessitate large sample volumes. Luminex technology allows the detection of multiple antibodies in a single experiment, but nonspecific binding can impair the results. Therefore, we examined the use of Escherichia coli lysates to reduce nonspecific binding and improve the results of liquid microarrays based on Luminex technology. Anti-bacteria antibodies were detected in human serum samples, as evidenced by high median fluorescence intensity (MFI) in assays performed with paramagnetic microspheres coupled with E. coli lysates. Moreover, the addition of an E. coli lysate as a blocker reduced the nonspecific binding of antigens produced by E. coli in a concentration-dependent manner. Tris-HCl reduced MFI values in negative samples, but did not affect MFI for positive samples. For microspheres coupled with different antigens, an E. coli lysate blocker significantly improved the fluorescence signals from positive samples. The addition of Tris-HCl and the E. coli lysate induced antigen-specific differences in MFI. This combination of the E. coli lysate blocker and Tris-HCl yielded a statistically significant improvement in MFI in the assays for Chagas disease and hepatitis C virus samples. However, for the Treponema pallidum p47 antigen improvement in MFI was only observed for the preparation with the E. coli blocker at a concentration of 3%. In conclusion, the addition of an E. coli lysate and Tris-HCl to the microarray assay reduced the nonspecific binding of human anti-bacteria antibodies and, therefore, increased the specific MFI.
    MeSH term(s) Antibodies, Bacterial/blood ; Antibodies, Protozoan/blood ; Antibody Specificity ; Antigens, Bacterial/genetics ; Antigens, Bacterial/immunology ; Enzyme-Linked Immunosorbent Assay ; Escherichia coli/chemistry ; Escherichia coli/immunology ; Hepatitis C Antibodies/blood ; Humans ; Immunoassay/methods ; Microarray Analysis ; Microspheres ; Recombinant Proteins/immunology ; Sensitivity and Specificity ; Treponema pallidum/chemistry ; Treponema pallidum/immunology ; Trypanosoma cruzi/immunology ; beta-Lactamases/immunology
    Chemical Substances Antibodies, Bacterial ; Antibodies, Protozoan ; Antigens, Bacterial ; Hepatitis C Antibodies ; Recombinant Proteins ; Tp47 protein, Treponema pallidum (EC 3.5.2.6) ; beta-Lactamases (EC 3.5.2.6)
    Language English
    Publishing date 2016-08
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 120142-6
    ISSN 1872-7905 ; 0022-1759
    ISSN (online) 1872-7905
    ISSN 0022-1759
    DOI 10.1016/j.jim.2016.05.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Gender Differences in Idiopathic Pulmonary Fibrosis: Are Men and Women Equal?

    Sesé, Lucile / Nunes, Hilario / Cottin, Vincent / Israel-Biet, Dominique / Crestani, Bruno / Guillot-Dudoret, Stephanie / Cadranel, Jacques / Wallaert, Benoit / Tazi, Abdellatif / Maître, Bernard / Prévot, Gregoire / Marchand-Adam, Sylvain / Hirschi, Sandrine / Dury, Sandra / Giraud, Violaine / Gondouin, Anne / Bonniaud, Philippe / Traclet, Julie / Juvin, Karine /
    Borie, Raphael / Carton, Zohra / Freynet, Olivia / Gille, Thomas / Planès, Carole / Valeyre, Dominique / Uzunhan, Yurdagül

    Frontiers in medicine

    2021  Volume 8, Page(s) 713698

    Abstract: Background: ...

    Abstract Background:
    Language English
    Publishing date 2021-08-05
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2021.713698
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: FPR2/ALX activation reverses LPS-induced vascular hyporeactivity in aorta and increases survival in a pneumosepsis model.

    Horewicz, Verônica Vargas / Crestani, Sandra / de Sordi, Regina / Rezende, Edir / Assreuy, Jamil

    European journal of pharmacology

    2015  Volume 746, Page(s) 267–273

    Abstract: The formylpeptide receptor 2 (FPR2/ALX) is a very promiscuous receptor, utilized by lipid and protein ligands that trigger pro- or anti-inflammatory responses. FPR2/ALX expression is increased in lung tissues of septic animals and its activation has a ... ...

    Abstract The formylpeptide receptor 2 (FPR2/ALX) is a very promiscuous receptor, utilized by lipid and protein ligands that trigger pro- or anti-inflammatory responses. FPR2/ALX expression is increased in lung tissues of septic animals and its activation has a beneficial therapeutic effect by controlling exacerbated inflammation. Although FPR2/ALX expression was observed in vascular smooth muscle cells, its role in vascular reactivity in inflammatory conditions has not been studied. In this study, we report that LPS increases FPR2/ALX expression in vascular smooth muscle cells (A7r5 cells) and aorta tissue, and that the selective agonist WKYMVm reverses LPS-induced vascular hyporeactivity in mouse aorta rings. Mice bearing pneumosepsis by Klebsiella pneumoniae and treated with WKYMVm recovered the reactivity to vasoconstrictors and the survival improved by 40%. As for the mechanisms involved, FPR2/ALX activation decreases NO production in LPS-stimulated cells and aorta, but it does not seem involve the regulation of NOS-2 expression. The molecular mechanism by which the peptide inhibits NO production still needs to be elucidated, but our data suggests an important role for NO in the WKYMVm beneficial effect observed in LPS injury and sepsis. In conclusion, our data suggest, for the first time, that a receptor, primarily described as a mediator of immune responses, may have an important role in the vascular dysfunctions observed in sepsis and may be a possible target for new therapeutic interventions.
    MeSH term(s) Animals ; Anti-Inflammatory Agents, Non-Steroidal/pharmacology ; Anti-Inflammatory Agents, Non-Steroidal/therapeutic use ; Aorta/drug effects ; Aorta/immunology ; Aorta/metabolism ; Cell Line ; Endothelium, Vascular/physiology ; Endothelium, Vascular/physiopathology ; In Vitro Techniques ; Klebsiella Infections/drug therapy ; Klebsiella Infections/metabolism ; Klebsiella Infections/microbiology ; Klebsiella Infections/physiopathology ; Klebsiella pneumoniae/drug effects ; Klebsiella pneumoniae/growth & development ; Klebsiella pneumoniae/immunology ; Lipopolysaccharides/toxicity ; Male ; Mice ; Muscle, Smooth, Vascular/drug effects ; Muscle, Smooth, Vascular/immunology ; Muscle, Smooth, Vascular/metabolism ; Nitric Oxide/agonists ; Nitric Oxide/antagonists & inhibitors ; Nitric Oxide/metabolism ; Oligopeptides/pharmacology ; Oligopeptides/therapeutic use ; Rats ; Receptors, Formyl Peptide/agonists ; Receptors, Formyl Peptide/metabolism ; Sepsis/drug therapy ; Sepsis/metabolism ; Sepsis/microbiology ; Sepsis/physiopathology ; Survival Analysis ; Vascular Resistance/drug effects ; Vasculitis/etiology ; Vasculitis/immunology ; Vasculitis/prevention & control
    Chemical Substances Anti-Inflammatory Agents, Non-Steroidal ; Lipopolysaccharides ; Oligopeptides ; Receptors, Formyl Peptide ; Trp-Lys-Tyr-Met-Val-Met ; formyl peptide receptor 2, mouse ; lipopolysaccharide, Escherichia coli O111 B4 ; tryptophyl-arginyl-tryptophyl-tryptophyl-tryptophyl-tryptophanamide ; Nitric Oxide (31C4KY9ESH)
    Language English
    Publishing date 2015-01-05
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80121-5
    ISSN 1879-0712 ; 0014-2999
    ISSN (online) 1879-0712
    ISSN 0014-2999
    DOI 10.1016/j.ejphar.2014.11.026
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Exercise attenuates dexamethasone-induced hypertension through an improvement of baroreflex activity independently of the renin-angiotensin system.

    Constantino, Paula B / Dionísio, Thiago J / Duchatsch, Francine / Herrera, Naiara A / Duarte, Josiane O / Santos, Carlos F / Crestani, Carlos C / Amaral, Sandra L

    Steroids

    2017  Volume 128, Page(s) 147–154

    Abstract: Dexamethasone-induced hypertension may be caused by baroreflex alterations or renin-angiotensin system (RAS) exacerbation. Aerobic training has been recommended for hypertension treatment, but the mechanisms responsible for reduction of arterial pressure ...

    Abstract Dexamethasone-induced hypertension may be caused by baroreflex alterations or renin-angiotensin system (RAS) exacerbation. Aerobic training has been recommended for hypertension treatment, but the mechanisms responsible for reduction of arterial pressure (AP) in dexamethasone (DEX) treated rats are still inconclusive.This study evaluated whether mechanisms responsible for training-induced attenuation of hypertension involve changes in autonomic nervous system and in RAS components. Rats underwent aerobic training protocol on treadmill or were kept sedentary for 8 weeks. Additionally, animals were treated with DEX during the last 10 days of exercise. Body weight (BW), AP and baroreflex activity were analyzed. Tibialis anterior (TA), soleus (SOL) and left ventricle (LV) were collected for evaluation of RAS components gene expression and protein levels. Dexamethasone decreased BW (20%), caused TA atrophy (16%) and increased systolic AP (SAP, 16%) as well as decreased baroreflex activity. Training attenuated SAP increase and improved baroreflex activity, although it did not prevent DEX-induced BW reduction and muscle atrophy. Neither DEX nor training caused expressive changes in RAS components. In conclusion, exercise training was effective in attenuating hypertension induced by DEX and this response may be mediated by a better autonomic balance through an improvement of baroreflex activity rather than changes in RAS components.
    MeSH term(s) Animals ; Arterial Pressure/physiology ; Baroreflex/physiology ; Blood Pressure ; Cardiovascular Diseases/physiopathology ; Cardiovascular Diseases/prevention & control ; Cardiovascular Diseases/therapy ; Dexamethasone/toxicity ; Exercise Therapy ; Heart Rate/physiology ; Hypertension/chemically induced ; Hypertension/physiopathology ; Hypertension/therapy ; Muscle, Skeletal/physiopathology ; Muscular Atrophy/physiopathology ; Muscular Atrophy/therapy ; Physical Conditioning, Animal/methods ; Rats ; Renin-Angiotensin System/genetics
    Chemical Substances Dexamethasone (7S5I7G3JQL)
    Language English
    Publishing date 2017-10-18
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80312-1
    ISSN 1878-5867 ; 0039-128X
    ISSN (online) 1878-5867
    ISSN 0039-128X
    DOI 10.1016/j.steroids.2017.10.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: A Prospective Accuracy Study of Prostate Imaging Reporting and Data System Version 2 on Multiparametric Magnetic Resonance Imaging in Detecting Clinically Significant Prostate Cancer With Whole-mount Pathology.

    Giannarini, Gianluca / Girometti, Rossano / Crestani, Alessandro / Rossanese, Marta / Calandriello, Mattia / Cereser, Lorenzo / Bednarova, Sandra / Battistella, Claudio / Sioletic, Stefano / Zuiani, Chiara / Valotto, Claudio / Ficarra, Vincenzo

    Urology

    2018  Volume 123, Page(s) 191–197

    Abstract: Objective: To assess the accuracy of Prostate Imaging Reporting and Data System version 2 (PI-RADS v2) in detecting clinically significant prostate cancer (csPCa) on multiparametric magnetic resonance imaging (mpMRI) using whole-mount sections after ... ...

    Abstract Objective: To assess the accuracy of Prostate Imaging Reporting and Data System version 2 (PI-RADS v2) in detecting clinically significant prostate cancer (csPCa) on multiparametric magnetic resonance imaging (mpMRI) using whole-mount sections after radical prostatectomy (RP) as reference standard.
    Methods: Forty-eight patients undergoing mpMRI before RP were prospectively enrolled. Two experienced radiologists independently scored and mapped imaging findings according to PI-RADS v2. One experienced uropathologist mapped cancers detected on whole-mount sections using the PI-RADS v2 sector scheme. Per-lesion and per-patient analyses were run. Primary outcomes were sensitivity and false discovery rate (FDR) in detecting csPCa using PI-RADS v2 score ≥3 and ≥4 as thresholds. Secondary outcome was inter-reader agreement.
    Results: On the per-lesion analysis, sensitivity and FDR at the PI-RADS v2 threshold score ≥3 were 0.75 and 0.17 for Reader 1, and 0.67 and 0.13 for Reader 2, respectively. At the PI-RADS v2 threshold score ≥4, sensitivity was slightly lower, and FDR nearly halved for both readers. On the per-patient analysis, sensitivity for csPCa at the PI-RADS v2 threshold score ≥3 was 0.85 for Reader 1, and 0.78 for Reader 2. At the PI-RADS v2 threshold score ≥4, sensitivity was slightly lower for both readers. Inter-reader agreement was substantial (k 0.72 and 0.65 for PI-RADS v2 threshold score ≥3 and ≥4, respectively).
    Conclusion: In our prospective study with pathology after RP as standard of reference, PI-RADS v2 showed good sensitivity in detecting csPCa on mpMRI with substantial agreement between 2 experienced readers. Threshold score ≥4 had lower FDR.
    MeSH term(s) Aged ; Data Systems ; Humans ; Magnetic Resonance Imaging ; Male ; Prospective Studies ; Prostatectomy ; Prostatic Neoplasms/diagnostic imaging ; Prostatic Neoplasms/pathology ; Prostatic Neoplasms/surgery ; Reproducibility of Results
    Language English
    Publishing date 2018-09-28
    Publishing country United States
    Document type Journal Article ; Validation Studies
    ZDB-ID 192062-5
    ISSN 1527-9995 ; 0090-4295
    ISSN (online) 1527-9995
    ISSN 0090-4295
    DOI 10.1016/j.urology.2018.07.067
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Reduction in renal blood flow following administration of norepinephrine and phenylephrine in septic rats treated with Kir6.1 ATP-sensitive and KCa1.1 calcium-activated K+ channel blockers.

    da Rosa Maggi Sant'Helena, Bruna / Guarido, Karla L / de Souza, Priscila / Crestani, Sandra / da Silva-Santos, J Eduardo

    European journal of pharmacology

    2015  Volume 765, Page(s) 42–50

    Abstract: We evaluated the effects of K+ channel blockers in the vascular reactivity of in vitro perfused kidneys, as well as on the influence of vasoactive agents in the renal blood flow of rats subjected to the cecal ligation and puncture (CLP) model of sepsis. ... ...

    Abstract We evaluated the effects of K+ channel blockers in the vascular reactivity of in vitro perfused kidneys, as well as on the influence of vasoactive agents in the renal blood flow of rats subjected to the cecal ligation and puncture (CLP) model of sepsis. Both norepinephrine and phenylephrine had the ability to increase the vascular perfusion pressure reduced in kidneys of rats subjected to CLP at 18 h and 36 h before the experiments. The non-selective K+ channel blocker tetraethylammonium, but not the Kir6.1 blocker glibenclamide, normalized the effects of phenylephrine in kidneys from the CLP 18 h group. Systemic administration of tetraethylammonium, glibenclamide, or the KCa1.1 blocker iberiotoxin, did not change the renal blood flow in control or septic rats. Norepinephrine or phenylephrine also had no influence on the renal blood flow of septic animals, but its injection in rats from the CLP 18 h group previously treated with either glibenclamide or iberiotoxin resulted in an exacerbated reduction in the renal blood flow. These results suggest an abnormal functionality of K+ channels in the renal vascular bed in sepsis, and that the blockage of different subtypes of K+ channels may be deleterious for blood perfusion in kidneys, mainly when associated with vasoactive drugs.
    MeSH term(s) Animals ; Blood Flow Velocity/drug effects ; Blood Flow Velocity/physiology ; KATP Channels/antagonists & inhibitors ; KATP Channels/physiology ; Large-Conductance Calcium-Activated Potassium Channel alpha Subunits/antagonists & inhibitors ; Large-Conductance Calcium-Activated Potassium Channel alpha Subunits/physiology ; Male ; Norepinephrine/pharmacology ; Phenylephrine/pharmacology ; Potassium Channel Blockers/pharmacology ; Potassium Channel Blockers/therapeutic use ; Rats ; Rats, Wistar ; Renal Circulation/drug effects ; Renal Circulation/physiology ; Sepsis/drug therapy ; Sepsis/physiopathology
    Chemical Substances KATP Channels ; Kcnma1 protein, rat ; Large-Conductance Calcium-Activated Potassium Channel alpha Subunits ; Potassium Channel Blockers ; uK-ATP-1 potassium channel ; Phenylephrine (1WS297W6MV) ; Norepinephrine (X4W3ENH1CV)
    Language English
    Publishing date 2015-10-15
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80121-5
    ISSN 1879-0712 ; 0014-2999
    ISSN (online) 1879-0712
    ISSN 0014-2999
    DOI 10.1016/j.ejphar.2015.08.014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Performance Assessment of a Trypanosoma cruzi Chimeric Antigen in Multiplex Liquid Microarray Assays.

    Santos, Fred Luciano Neves / Celedon, Paola Alejandra Fiorani / Zanchin, Nilson Ivo Tonin / Leitolis, Amanda / Crestani, Sandra / Foti, Leonardo / de Souza, Wayner Vieira / Gomes, Yara de Miranda / Krieger, Marco Aurélio

    Journal of clinical microbiology

    2017  Volume 55, Issue 10, Page(s) 2934–2945

    Abstract: Diagnosing chronic Chagas disease (CD) requires antibody-antigen detection methods, which are traditionally based on enzymatic assay techniques whose performance depend on the type and quality of antigen used. Previously, 4 recombinant chimeric proteins ... ...

    Abstract Diagnosing chronic Chagas disease (CD) requires antibody-antigen detection methods, which are traditionally based on enzymatic assay techniques whose performance depend on the type and quality of antigen used. Previously, 4 recombinant chimeric proteins from the Instituto de Biologia Molecular do Paraná (IBMP-8.1 to 8.4) comprising immuno-dominant regions of diverse
    MeSH term(s) Antibodies, Protozoan/blood ; Antibodies, Protozoan/immunology ; Antigens, Protozoan/immunology ; Chagas Disease/diagnosis ; Chagas Disease/parasitology ; Cross Reactions/immunology ; Enzyme-Linked Immunosorbent Assay/methods ; False Negative Reactions ; Humans ; Leishmania/immunology ; Microarray Analysis/methods ; Recombinant Proteins/immunology ; Trypanosoma cruzi/immunology
    Chemical Substances Antibodies, Protozoan ; Antigens, Protozoan ; Recombinant Proteins
    Language English
    Publishing date 2017-07-19
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 390499-4
    ISSN 1098-660X ; 0095-1137
    ISSN (online) 1098-660X
    ISSN 0095-1137
    DOI 10.1128/JCM.00851-17
    Database MEDical Literature Analysis and Retrieval System OnLINE

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