Acute nitric oxide synthase inhibition induces greater increases in blood pressure in female versus male Wistar Kyoto rats

Abstract Nitric oxide (NO) contributes to blood pressure (BP) regulation via its vasodilatory and anti‐inflammatory properties. We and others previously reported sex differences in BP in normotensive and hypertensive rat models where females have lower BP than age‐matched males. As females are known...

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Main Authors: Ahmed A. Elmarakby, Karim M. Saad, G. Ryan Crislip, Jennifer C. Sullivan
Format: Article
Language:English
Published: Wiley 2023-08-01
Series:Physiological Reports
Subjects:
Online Access:https://doi.org/10.14814/phy2.15771
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author Ahmed A. Elmarakby
Karim M. Saad
G. Ryan Crislip
Jennifer C. Sullivan
author_facet Ahmed A. Elmarakby
Karim M. Saad
G. Ryan Crislip
Jennifer C. Sullivan
author_sort Ahmed A. Elmarakby
collection DOAJ
description Abstract Nitric oxide (NO) contributes to blood pressure (BP) regulation via its vasodilatory and anti‐inflammatory properties. We and others previously reported sex differences in BP in normotensive and hypertensive rat models where females have lower BP than age‐matched males. As females are known to have greater NO bioavailability than age‐matched males, the current study was designed to test the hypothesis that anesthetized female normotensive Wistar Kyoto rats (WKY) are more responsive to acute NOS inhibition‐induced increases in BP compared to male WKY. Twelve‐week‐old male and female WKY were randomized to infusion of the nonspecific NOS inhibitor NG‐nitro‐L‐arginine methyl ester (L‐NAME, 1 mg/kg/min) or selective NOS1 inhibition with vinyl‐L‐NIO (VNIO, 0.5 mg/kg/min) for 60 min. Mean arterial BP, glomerular filtration rate (GFR), urine volume, and electrolyte excretion were assessed before, and during L‐NAME or VNIO infusion. L‐NAME and VNIO significantly increased BP in both sexes; however, the increase in BP with L‐NAME infusion was greater in females versus males compared to baseline BP values. Acute infusion of neither L‐NAME nor VNIO for 60 min altered GFR in either sex. However, urine volume, sodium, chloride and potassium excretion levels increased comparably in male and female WKY with L‐NAME and VNIO infusion. Our findings suggest sex differences in BP responses to acute non‐isoform‐specific NOS inhibition in WKY, with females being more responsive to L‐NAME‐induced elevations in BP relative to male WKY. However, sex differences in the BP response did not coincide with sex differences in renal hemodynamic responses to acute NOS inhibition.
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spelling doaj.art-52370cb3a48942ad92c9c1b5f1cdec7b2023-12-11T03:55:35ZengWileyPhysiological Reports2051-817X2023-08-011115n/an/a10.14814/phy2.15771Acute nitric oxide synthase inhibition induces greater increases in blood pressure in female versus male Wistar Kyoto ratsAhmed A. Elmarakby0Karim M. Saad1G. Ryan Crislip2Jennifer C. Sullivan3Departments of Oral Biology & Diagnostic Sciences Augusta University Augusta Georgia USADepartments of Oral Biology & Diagnostic Sciences Augusta University Augusta Georgia USADepartments of Physiology Augusta University Augusta Georgia USADepartments of Physiology Augusta University Augusta Georgia USAAbstract Nitric oxide (NO) contributes to blood pressure (BP) regulation via its vasodilatory and anti‐inflammatory properties. We and others previously reported sex differences in BP in normotensive and hypertensive rat models where females have lower BP than age‐matched males. As females are known to have greater NO bioavailability than age‐matched males, the current study was designed to test the hypothesis that anesthetized female normotensive Wistar Kyoto rats (WKY) are more responsive to acute NOS inhibition‐induced increases in BP compared to male WKY. Twelve‐week‐old male and female WKY were randomized to infusion of the nonspecific NOS inhibitor NG‐nitro‐L‐arginine methyl ester (L‐NAME, 1 mg/kg/min) or selective NOS1 inhibition with vinyl‐L‐NIO (VNIO, 0.5 mg/kg/min) for 60 min. Mean arterial BP, glomerular filtration rate (GFR), urine volume, and electrolyte excretion were assessed before, and during L‐NAME or VNIO infusion. L‐NAME and VNIO significantly increased BP in both sexes; however, the increase in BP with L‐NAME infusion was greater in females versus males compared to baseline BP values. Acute infusion of neither L‐NAME nor VNIO for 60 min altered GFR in either sex. However, urine volume, sodium, chloride and potassium excretion levels increased comparably in male and female WKY with L‐NAME and VNIO infusion. Our findings suggest sex differences in BP responses to acute non‐isoform‐specific NOS inhibition in WKY, with females being more responsive to L‐NAME‐induced elevations in BP relative to male WKY. However, sex differences in the BP response did not coincide with sex differences in renal hemodynamic responses to acute NOS inhibition.https://doi.org/10.14814/phy2.15771blood pressureL‐NAMErenal hemodynamicssexVNIOWKY
spellingShingle Ahmed A. Elmarakby
Karim M. Saad
G. Ryan Crislip
Jennifer C. Sullivan
Acute nitric oxide synthase inhibition induces greater increases in blood pressure in female versus male Wistar Kyoto rats
Physiological Reports
blood pressure
L‐NAME
renal hemodynamics
sex
VNIO
WKY
title Acute nitric oxide synthase inhibition induces greater increases in blood pressure in female versus male Wistar Kyoto rats
title_full Acute nitric oxide synthase inhibition induces greater increases in blood pressure in female versus male Wistar Kyoto rats
title_fullStr Acute nitric oxide synthase inhibition induces greater increases in blood pressure in female versus male Wistar Kyoto rats
title_full_unstemmed Acute nitric oxide synthase inhibition induces greater increases in blood pressure in female versus male Wistar Kyoto rats
title_short Acute nitric oxide synthase inhibition induces greater increases in blood pressure in female versus male Wistar Kyoto rats
title_sort acute nitric oxide synthase inhibition induces greater increases in blood pressure in female versus male wistar kyoto rats
topic blood pressure
L‐NAME
renal hemodynamics
sex
VNIO
WKY
url https://doi.org/10.14814/phy2.15771
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