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  • Ovid Technologies (Wolters Kluwer Health)  (13)
  • 1
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2008
    In:  NeuroReport Vol. 19, No. 9 ( 2008-06-11), p. 981-985
    In: NeuroReport, Ovid Technologies (Wolters Kluwer Health), Vol. 19, No. 9 ( 2008-06-11), p. 981-985
    Materialart: Online-Ressource
    ISSN: 0959-4965
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2008
    ZDB Id: 2031485-1
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2001
    In:  Neurosurgery Vol. 49, No. 2 ( 2001-08), p. 542-
    In: Neurosurgery, Ovid Technologies (Wolters Kluwer Health), Vol. 49, No. 2 ( 2001-08), p. 542-
    Materialart: Online-Ressource
    ISSN: 0148-396X
    RVK:
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2001
    ZDB Id: 1491894-8
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2001
    In:  Neurosurgery Vol. 49, No. 2 ( 2001-08-01), p. 542-542
    In: Neurosurgery, Ovid Technologies (Wolters Kluwer Health), Vol. 49, No. 2 ( 2001-08-01), p. 542-542
    Materialart: Online-Ressource
    ISSN: 0148-396X , 1524-4040
    RVK:
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2001
    ZDB Id: 1491894-8
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2011
    In:  Otology & Neurotology Vol. 32, No. 5 ( 2011-07), p. 719-
    In: Otology & Neurotology, Ovid Technologies (Wolters Kluwer Health), Vol. 32, No. 5 ( 2011-07), p. 719-
    Materialart: Online-Ressource
    ISSN: 1531-7129
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2011
    ZDB Id: 2058738-7
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2018
    In:  Anesthesia & Analgesia Vol. 127, No. 4 ( 2018-10), p. 1051-1057
    In: Anesthesia & Analgesia, Ovid Technologies (Wolters Kluwer Health), Vol. 127, No. 4 ( 2018-10), p. 1051-1057
    Kurzfassung: Diabetes mellitus affects 9.3% of the US population and increases risks of surgery and complications. Diabetic neuropathic pain (DNP), one of the main consequences of diabetes mellitus, is extremely difficult to treat. Current medications yield limited benefits and/or have severe adverse effects. Therefore, new, effective treatment is needed. METHODS: Streptozotocin at 55 mg/kg was injected intraperitoneally in rats to induce diabetes mellitus. Diabetic rats exhibiting neuropathic pain underwent intrathecal injection of purified agrin proteins at various doses and were then tested for tactile allodynia to evaluate whether DNP was inhibited. The agrin effects were also analyzed with patch-clamp recording on spinal cord slices. RESULTS: Fifty–kilo Dalton agrin (Agr50) at 0.2 and 2 ng suppressed DNP when given intrathecally, while 25- and 75-kDa agrin (Agr25, Agr75) had little effect. The suppressive effect of Agr50 lasted 4 hours after a single bolus injection. The difference in effects of Agr50 on mean withdrawal threshold (4.6 ± 2.2 g before treatment to 26 ± 0 g after treatment) compared with that of Agr25 (4.9 ± 2.0 g to 4.9 ± 2.0 g) and Agr75 (5.3 ± 2.3 g to 9.2 ± 2.5 g) was highly significant ( P 〈 .01). On spinal cord slices, Agr50 increased spontaneous GABAergic current activities, suggesting increased spontaneous inhibitory postsynaptic currents and action potential firing rate from GABA neurons, whereas Agr25 and Agr75 had no such effect. CONCLUSIONS: Agr50 had a potent suppressive effect on DNP and increased spontaneous inhibitory postsynaptic currents and action potential firing rate from GABA neurons. Therefore, Agr50 may provide a potential therapy for DNP.
    Materialart: Online-Ressource
    ISSN: 0003-2999
    RVK:
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2018
    ZDB Id: 2018275-2
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 6
    In: Neurosurgery, Ovid Technologies (Wolters Kluwer Health), Vol. 66, No. Supplement 1 ( 2019-09), p. 310-839
    Materialart: Online-Ressource
    ISSN: 0148-396X
    RVK:
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2019
    ZDB Id: 1491894-8
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 7
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2013
    In:  Otology & Neurotology Vol. 34, No. 1 ( 2013-01), p. 8-
    In: Otology & Neurotology, Ovid Technologies (Wolters Kluwer Health), Vol. 34, No. 1 ( 2013-01), p. 8-
    Materialart: Online-Ressource
    ISSN: 1531-7129
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2013
    ZDB Id: 2058738-7
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 8
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2017
    In:  Circulation Research Vol. 121, No. 1 ( 2017-06-23), p. 43-55
    In: Circulation Research, Ovid Technologies (Wolters Kluwer Health), Vol. 121, No. 1 ( 2017-06-23), p. 43-55
    Kurzfassung: Neurogenic hypertension is characterized by an increase in sympathetic activity and often resistance to drug treatments. We previously reported that it is also associated with a reduction of angiotensin-converting enzyme type 2 (ACE2) and an increase in a disintegrin and metalloprotease 17 (ADAM17) activity in experimental hypertension. In addition, while multiple cells within the central nervous system have been involved in the development of neurogenic hypertension, the contribution of ADAM17 has not been investigated. Objective: To assess the clinical relevance of this ADAM17-mediated ACE2 shedding in hypertensive patients and further identify the cell types and signaling pathways involved in this process. Methods and Results: Using a mass spectrometry-based assay, we identified ACE2 as the main enzyme converting angiotensin II into angiotensin-(1–7) in human cerebrospinal fluid. We also observed an increase in ACE2 activity in the cerebrospinal fluid of hypertensive patients, which was correlated with systolic blood pressure. Moreover, the increased level of tumor necrosis factor-α in those cerebrospinal fluid samples confirmed that ADAM17 was upregulated in the brain of hypertensive patients. To further assess the interaction between brain renin–angiotensin system and ADAM17, we generated mice lacking angiotensin II type 1 receptors specifically on neurons. Our data reveal that despite expression on astrocytes and other cells types in the brain, ADAM17 upregulation during deoxycorticosterone acetate–salt hypertension occurs selectively on neurons, and neuronal angiotensin II type 1 receptors are indispensable to this process. Mechanistically, reactive oxygen species and extracellular signal-regulated kinase were found to mediate ADAM17 activation. Conclusions: Our data demonstrate that angiotensin II type 1 receptors promote ADAM17-mediated ACE2 shedding in the brain of hypertensive patients, leading to a loss in compensatory activity during neurogenic hypertension.
    Materialart: Online-Ressource
    ISSN: 0009-7330 , 1524-4571
    RVK:
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2017
    ZDB Id: 1467838-X
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 9
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2014
    In:  Hypertension Vol. 64, No. suppl_1 ( 2014-09)
    In: Hypertension, Ovid Technologies (Wolters Kluwer Health), Vol. 64, No. suppl_1 ( 2014-09)
    Kurzfassung: ACE2 (Angiotensin Converting Enzyme type 2) is involved in the conversion of the vasoconstrictor peptide Angiotensin (Ang)-II into its vasodilatory metabolite Ang-(1-7), thereby offering a new perspective for the treatment of cardiovascular diseases associated with over-activity of the renin-angiotensin system. Our group recently reported that ACE2 shedding, a process by which ACE2 is cleaved from the plasma membrane and secreted into the surrounding milieu, contributes to the loss of the enzyme’s compensatory activity in the central nervous system (CNS) during the development of experimental hypertension. The objective of this study was to determine whether ACE2 shedding is taking place in the CNS of patients during hypertension. Unused cerebrospinal fluid, collected from patients (17 males and 27 females, aged 22-66) for diagnostic purposes, was divided in 3 groups: normotensive (n=23), hypertensive (n=9), and hypertensive controlled with medication (n=12). In addition, blood pressure values and current medications were recorded. While ELISA lacked sensitivity, soluble levels of hACE2 (sACE2) could be detected by Mass spectrometry-based RAS-Fingerprint™ in all patients. Validation experiments (n=16) indicated that pre-treatment with MLN4760 (ACE2 inhibitor) abolished the conversion of Ang-II to Ang-(1-7) by 76 ±3 %, suggesting that ACE2 is the main enzyme converting Ang-II to Ang-(1-7) in human CSF. In hypertensive patients not taking blood pressure medications, (Systolic: 157 ±10, Diastolic: 95 ±7 mmHg; n=6) CSF sACE2 activity was significantly higher (21.7 ±8.3 AU; P 〈 0.05) than in normotensive (Systolic: 114 ±4, Diastolic: 75 ±4 mmHg; n=15) patients (6.6 ±0.9 AU). However, in patients with controlled hypertension (Systolic: 129 ±6, Diastolic: 86 ±5 mmHg; n=5), CSF sACE2 levels were normalized (6.9 ±1.9 AU). Comparison of systolic or diastolic blood pressure vs. sACE2 activity levels showed no significant correlation. These data suggest that ACE2 shedding is taking place in the CNS of hypertensive patients. Soluble ACE2 activity in the CSF is correlated with high blood pressure and could be used as a biomarker of neurogenic hypertension. AU: arbitrary unit.
    Materialart: Online-Ressource
    ISSN: 0194-911X , 1524-4563
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2014
    ZDB Id: 2094210-2
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 10
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2012
    In:  Stroke Vol. 43, No. suppl_1 ( 2012-02)
    In: Stroke, Ovid Technologies (Wolters Kluwer Health), Vol. 43, No. suppl_1 ( 2012-02)
    Kurzfassung: INTRODUCTION: Vasospasm following aneurysmal subarachnoid hemorrhage is a very extensively studied source of morbidity and mortality. Numerous treatment regiments have been investigated and published. A recently published article discussed the use of prolonged infusion of verapamil through an indwelling catheter as an effective treatment for medically refractory severe vasospasm. The goal of our study is to report our institution's experience with this method of treatment. METHODS & MATERIALS: All patients with medically refractory vasospasm from July 2009 through August 2011 were included in the study. A retrospective review of data was compiled. In particular, age, sex, aneurysm location, aneurysm treatment, intra-arterial treatment fo vasospasm, dosages and times of medication infusion, and presence of new ischemia or progression of ischemia on CT scan were investigated. RESULTS: A total of 13 treatments were administered. Nicardipine was used in two treatments, and verapamil was used in the remaining eleven treatments. The doses of nicardipine were 10mg and 49 mg, and were infused over 20 min and 75 min respectively. The doses of verapamil ranged from 41 mg to 200 mg. One patient was treated with both nicardipine and verapamil at one treatment session. The infusion times ranged from 25 min to 22 hr. Between 1 and 3 vessels were treated per patient resulting in a total of 19 vessels treated. The number of treatments per patient ranged from one to two. Review of pre- and post-treatment CT scans revealed worsening of ischemic changes in 9 of the 13 treatments, while the remaining 4 treatments showed no change or progression of ischemic changes on imaging. One patient had a conversion to a hemorrhagic infarct from an inschemic infarct after a treatment. CONCLUSIONS: Upon reviewing our data we have come to the conclusion that prolonged infusion of calcium channel blockers is not an effective treatment for medically refractory severe vasospasm. After 13 treatments we have decided to not continue with this treatment. Therefore, we believe that angioplasty is still the gold standard for treatment of medically refractory vasospasm.
    Materialart: Online-Ressource
    ISSN: 0039-2499 , 1524-4628
    RVK:
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2012
    ZDB Id: 1467823-8
    Standort Signatur Einschränkungen Verfügbarkeit
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