TY - JOUR
T1 - Vasa recta pericyte density is negatively associated with vascular congestion in the renal medulla following ischemia reperfusion in rats
AU - Crislip, G. Ryan
AU - O’Connor, Paul M.
AU - Wei, Qingqing
AU - Sullivan, Jennifer C.
N1 - Funding Information:
This work was supported by the American Heart Association (Predoctoral Fellowship 15PRE25850008 to G. R. Crislip) and National Institutes of Health (1P01HL-134604-01 and R01HL-127091 to J. C. Sullivan; 1P01HL-134604-01 to P. M. O’Connor).
Publisher Copyright:
© 2017 the American Physiological Society.
PY - 2017/11/29
Y1 - 2017/11/29
N2 - Recent evidence suggests that a greater density of pericytes in renal cadaveric allografts is associated with better recovery following transplant. The physiological mechanism(s) through which pericyte density may be beneficial is not well understood. The goal of this study was to test the hypothesis that lower medullary pericyte density is associated with greater renal injury following ischemia reperfusion (IR) in a rat model, providing a basis for future studies to better understand pericytes in a pathological environment. To test our hypothesis, we determined the association between medullary pericyte density and renal injury in spontaneously hypertensive rats (SHR) following 45 min of warm bilateral IR. We found that there was a significant negative relationship between pericyte density and plasma creatinine (slope=-0.03, P = 0.02) and blood urea nitrogen (slope=-0.5, P = 0.01) in female but not male SHR. Pericyte density was negatively associated with medullary peritubular capillary (PT) congestion in both sexes following IR (male: slope=-0.04, P = 0.009; female: slope=-0.03, P = 0.0001). To further test this relationship, we used a previously reported method to reduce pericyte density in SHR. Medullary erythrocyte congestion in vasa recta (VR) and PT significantly increased following IR in both sexes when pericyte density was pharmacologically decreased (VR: P = 0.03; PT: P = 0.03). Our data support the hypothesis that pericyte density is negatively associated with the development of IR injury in SHR, which may be mediated by erythrocyte congestion in the medullary vasculature.
AB - Recent evidence suggests that a greater density of pericytes in renal cadaveric allografts is associated with better recovery following transplant. The physiological mechanism(s) through which pericyte density may be beneficial is not well understood. The goal of this study was to test the hypothesis that lower medullary pericyte density is associated with greater renal injury following ischemia reperfusion (IR) in a rat model, providing a basis for future studies to better understand pericytes in a pathological environment. To test our hypothesis, we determined the association between medullary pericyte density and renal injury in spontaneously hypertensive rats (SHR) following 45 min of warm bilateral IR. We found that there was a significant negative relationship between pericyte density and plasma creatinine (slope=-0.03, P = 0.02) and blood urea nitrogen (slope=-0.5, P = 0.01) in female but not male SHR. Pericyte density was negatively associated with medullary peritubular capillary (PT) congestion in both sexes following IR (male: slope=-0.04, P = 0.009; female: slope=-0.03, P = 0.0001). To further test this relationship, we used a previously reported method to reduce pericyte density in SHR. Medullary erythrocyte congestion in vasa recta (VR) and PT significantly increased following IR in both sexes when pericyte density was pharmacologically decreased (VR: P = 0.03; PT: P = 0.03). Our data support the hypothesis that pericyte density is negatively associated with the development of IR injury in SHR, which may be mediated by erythrocyte congestion in the medullary vasculature.
KW - Erythrocyte trapping
KW - Ischemia reperfusion injury
KW - Sex difference
KW - Spontaneously hypertensive rats
UR - http://www.scopus.com/inward/record.url?scp=85036522087&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85036522087&partnerID=8YFLogxK
U2 - 10.1152/ajprenal.00261.2017
DO - 10.1152/ajprenal.00261.2017
M3 - Article
C2 - 28794065
AN - SCOPUS:85036522087
SN - 0363-6135
VL - 313
SP - F1097-F1105
JO - American Journal of Physiology - Heart and Circulatory Physiology
JF - American Journal of Physiology - Heart and Circulatory Physiology
IS - 5
ER -