INT2630
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
This causes their plasma concentrations to increase with time, since SHBG is induced by ethinylestradiol even in doses of 30 micrograms daily. | |||||||||||||||
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The pretreatment of NG-monomethyl-L-arginine dose-dependently reduced the elevation of ABP but did not completely abolish it. | |||||||||||||||
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Results indicate that inhibition of nitric oxide (NO) might be responsible in part for the elevation of ABP, and the degree of the elevation would be dependent on the degree of contribution of NO to the regulation of ABP. | |||||||||||||||
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Pretreatment with various blockers did not abolish the elevation of ABP. | |||||||||||||||
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SHBG concentrations were elevated in the Large-tumor group. | |||||||||||||||
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Administration of both drugs produced a significant suppression of elevation of SBP, and produced a significant elevation of pain sensitivity. | |||||||||||||||
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Levels of sex hormone binding globulin (SHBG), a protein increased by EE to which NET binds, were also examined. | |||||||||||||||
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In both phase I and II studies arzoxifene showed similar endocrine effects of decreasing FSH and LH levels with increasing SHBG levels as had been reported with tamoxifen (Lønning et al. 1995; Kostoglou-Athanassiou et al. 1997). | |||||||||||||||
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Although interpretation was limited by the small sample size, arzoxifene appeared to lower proliferation markers including proliferating cell nuclear antigen (PCNA), insulin-like growth factor (IGF)-1 and IGF-binding protein-3 (IGFBP-3), decrease estrogen expression and LH levels, and increase SHBG levels. | |||||||||||||||
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There was a significant decrease in follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels, along with an increase in sex hormone-binding globulin (SHBG). | |||||||||||||||
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This increase in SHBG could be interpreted as a marker of improved insulin sensitivity, nicely fitting the finding of improved glycemic control in the paroxetine group. | |||||||||||||||
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In the paroxetine group a superior increase in SHBG levels were observed. | |||||||||||||||
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The patients had higher levels of testosterone and SHBG than did the controls (p = 0.04 and p = 0.03, respectively). | |||||||||||||||
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Patients with advanced liver disease and low ascitic fluid protein concentrations seem to have an increased susceptibility to SBP. | |||||||||||||||
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The maximal response of SBP to phenylephrine or sodium nitroprusside and the corresponding maximal reflex change in pulse interval were plotted for each drug. | |||||||||||||||
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Moreover, regitine was shown to inhibit the increase of mABP in morphine withdrawal rats, but can not inhibit the increase of HR. | |||||||||||||||
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There was a significant decrease in follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels, along with an increase in sex hormone-binding globulin (SHBG). | |||||||||||||||
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The LF component of SBP (SBP-LF) increases in conditions associated with various sympathetic activations [13-15]. | |||||||||||||||
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The LF component of SBP (SBP-LF) increases in conditions associated with various sympathetic activations [13-15]. | |||||||||||||||
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In the presence of atenolol 2 mg kg(-1) h(-1), clonidine 10-100 microg kg(-1) i.v. evoked a significant reduction in SBP, a large increase of CVM firing rate from a very low base line [0.16 (sd 0.28) to 1.37 (1.21) spikes s(-1), n=7 cells], and increased the slope of the cardiac baroreflex analysed at the CVM level or at the heart level. sds of SBP were reduced, and that of RR interval was increased. | |||||||||||||||
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General Comments
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