Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Sino-aortic denervation (SAD) is employed in cats to evaluate the baroreflex influence on blood pressure (BP) and pulse interval (PI) spectral components from 0.00008 to 0.9 Hz as assessed by FFT wide-band spectra and their 1/f modelling; and the linear coupling between BP and PI and between systolic and diastolic BP as assessed by coherence analysis. Specific procedures have been developed to obtain an effective smoothing of spectra and coherence functions. SAD induced an increase in BP powers from 0.03 to 0.0006 Hz and a power reduction of most of the remaining BP components; a reduction of PI powers at all frequencies; marked deviations of BP spectra from the 1/f trend; a reduction of the coherence between BP and PI from 0.12 to 0.5 Hz and a coherence enhancement at lower frequencies. These findings indicate that the arterial baroreflex modulates both fast and slow spectral components of BP and PI; homogeneously enhances PI fluctuations at all frequencies; produces differentiated effects on BP fluctuations along the frequency axis; and at low frequencies exerts the buffering action on BP through strategies which reduce the BP-PI linear link.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1007/BF02520018 | DOI Listing |
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