Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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The architecture of kidney vasculature is essential the organ's specialised functions, yet is challenging to structurally map in an intact human organ. Here, we combined hierarchical phase-contrast tomography (HiP-CT) with topology network analysis to enable quantitative assessment of the intact human kidney vasculature, from the renal artery to interlobular arteries. Comparison with kidney vascular maps described for rodents revealed similar topologies to human, but human kidney vasculature possessed a significantly sharper decrease in radius from hilum to cortex, deviating from theoretically optimal flow resistance for smaller vessels. Structural differences in kidney hilar, medullary and cortical vasculature reflected unique functional adaptations of each zone. This work represents the first time the arterial vasculature of an intact human kidney has been mapped beyond segmental arteries, potentiating novel computational models of kidney vascular flow in humans. Our analyses have implications for understanding how blood vessel structure collectively scales to facilitate specialised functions in human organs.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12408821 | PMC |
http://dx.doi.org/10.1038/s44303-025-00090-2 | DOI Listing |