Javascript must be enabled to continue!
Inhibition of NLRP3 attenuates DOCA-Salt-Induced Hypertrophy and Endothelial Dysfunction in Male But Not Female Rats
View through CrossRef
The immune system has been implicated in the development of
hypertension and how the immune system is activated is of high interest. The
NLRP3 inflammasome has been shown to contribute to the development of
DOCA-salt hypertension in males, and we recently found that T cells
contribute to sex differences in blood pressure with DOCA-salt. The goal of
the current study was to test the hypothesis that males exhibit greater
increases in NLRP3 with DOCA than females and that NLRP3 contributes to
DOCA-salt-induced changes in end-organ hypertrophy. To determine the impact
of DOCA on NLRP3, 11-week-old male and female Sprague Dawley (SD) rats were
uninephrectomized (UNX) and randomized to control or 3 weeks of DOCA-salt
treatment (n=6/group). NLRP3 and IL1β mRNA expression were measured via
RT-PCR and data were compared via 2-way ANOVA. Renal NLRP3 and IL1β
expression were greater in UNX control males than females. DOCA increased
expression in both sexes, although the increases were greater in males
(NLRP3: P interaction =0.03, P
treatment <0.0001, P sex
=0.0014; IL1β: P interaction =0.02, P
treatment <0.0001, P sex
=0.052). Additional UNX male and female SD rats were then randomized
(n=6-10/group) to DOCA (200 mg) + saline or DOCA + saline + MCC950 (10
mg/kg/day). At 14 wks of age, rats were weighed and euthanized. The heart,
spleen and remaining kidney were weighed and data were compared via 2-way
ANOVA. The effectiveness of MCC950 was assessed by measuring renal NLPR3
mRNA expression at the end of the experiment. 3 weeks of MCC950 decreased
NLRP3 in both sexes, although expression remained greater in males (P
interaction =0.44, P treatment
=0.0043, P sex =0.0001). 3 weeks of MCC950 attenuated
increases in body weight in both sexes, although males of both groups
weighed more than females. Due to differences in body weights, heart, spleen
and kidney weights were normalized to body weight. Interestingly, heart:body
weight ratio decreased in males and increased in females with MCC950
treatment. Neither splenic or kidney:body weight ratios were significantly
altered by MCC950 treatment. These data support a role for the NLRP3
inflammasome to contribute to DOCA-salt induced increases in inflammation,
and therefore increases in blood pressure, particularly in males.
This work was supported by U54HL169191 (J.C.S and M.J.R), BX002604
(M.J.R)
This abstract was presented at the American Physiology Summit 2025 and
is only available in HTML format. There is no downloadable file or PDF
version. The Physiology editorial board was not involved in the peer review
process.
American Physiological Society
Title: Inhibition of NLRP3 attenuates DOCA-Salt-Induced Hypertrophy and
Endothelial Dysfunction in Male But Not Female Rats
Description:
The immune system has been implicated in the development of
hypertension and how the immune system is activated is of high interest.
The
NLRP3 inflammasome has been shown to contribute to the development of
DOCA-salt hypertension in males, and we recently found that T cells
contribute to sex differences in blood pressure with DOCA-salt.
The goal of
the current study was to test the hypothesis that males exhibit greater
increases in NLRP3 with DOCA than females and that NLRP3 contributes to
DOCA-salt-induced changes in end-organ hypertrophy.
To determine the impact
of DOCA on NLRP3, 11-week-old male and female Sprague Dawley (SD) rats were
uninephrectomized (UNX) and randomized to control or 3 weeks of DOCA-salt
treatment (n=6/group).
NLRP3 and IL1β mRNA expression were measured via
RT-PCR and data were compared via 2-way ANOVA.
Renal NLRP3 and IL1β
expression were greater in UNX control males than females.
DOCA increased
expression in both sexes, although the increases were greater in males
(NLRP3: P interaction =0.
03, P
treatment <0.
0001, P sex
=0.
0014; IL1β: P interaction =0.
02, P
treatment <0.
0001, P sex
=0.
052).
Additional UNX male and female SD rats were then randomized
(n=6-10/group) to DOCA (200 mg) + saline or DOCA + saline + MCC950 (10
mg/kg/day).
At 14 wks of age, rats were weighed and euthanized.
The heart,
spleen and remaining kidney were weighed and data were compared via 2-way
ANOVA.
The effectiveness of MCC950 was assessed by measuring renal NLPR3
mRNA expression at the end of the experiment.
3 weeks of MCC950 decreased
NLRP3 in both sexes, although expression remained greater in males (P
interaction =0.
44, P treatment
=0.
0043, P sex =0.
0001).
3 weeks of MCC950 attenuated
increases in body weight in both sexes, although males of both groups
weighed more than females.
Due to differences in body weights, heart, spleen
and kidney weights were normalized to body weight.
Interestingly, heart:body
weight ratio decreased in males and increased in females with MCC950
treatment.
Neither splenic or kidney:body weight ratios were significantly
altered by MCC950 treatment.
These data support a role for the NLRP3
inflammasome to contribute to DOCA-salt induced increases in inflammation,
and therefore increases in blood pressure, particularly in males.
This work was supported by U54HL169191 (J.
C.
S and M.
J.
R), BX002604
(M.
J.
R)
This abstract was presented at the American Physiology Summit 2025 and
is only available in HTML format.
There is no downloadable file or PDF
version.
The Physiology editorial board was not involved in the peer review
process.
Related Results
The Transcription Factor Gfi1 Negatively Regulates NLRP3 inflammasome-Mediated IL-1β Secretion in Macrophages
The Transcription Factor Gfi1 Negatively Regulates NLRP3 inflammasome-Mediated IL-1β Secretion in Macrophages
Abstract
Background: IL-1β secretion is tightly controlled at the transcriptional and post-translational levels. The NLRP3 inflammasome, a multiprotein complex compo...
ROLE OF CHEMOKINE RECEPTOR 2 IN RENAL INJURY DURING DOCA-SALT HYPERTENSION
ROLE OF CHEMOKINE RECEPTOR 2 IN RENAL INJURY DURING DOCA-SALT HYPERTENSION
Objectives
This study was designed to determine the role of chemokine receptor 2 (CCR2), a receptor of MCP-1, in the development of salt-sensitive hypertension-in...
Plasma atrial natriuretic peptide in DOCA‐NaCl‐treated rats
Plasma atrial natriuretic peptide in DOCA‐NaCl‐treated rats
In order to assess the possible role of atrial natriuretic peptide (ANP) in the development of deoxycorticosterone (DOCA)‐NaCl‐induced hypertension, plasma immunoreactive ANP conce...
Effect of miR-223-3p on cell pyroptosis in myelodysplastic syndrome and its
mechanism via regulating the expression of NLRP3
Effect of miR-223-3p on cell pyroptosis in myelodysplastic syndrome and its
mechanism via regulating the expression of NLRP3
This study aimed to investigate the regulatory mechanism of the miR-223-3p/NLRP3 signaling axis in
the progression of myelodysplastic syndrome (MDS). For this purpose, SKM-1 cells ...
Abstract 7521: Tumor NLRP3 inflammasome activity mediates resistance to Anti-PD-1 immunotherapy in advanced gastroesophageal cancer
Abstract 7521: Tumor NLRP3 inflammasome activity mediates resistance to Anti-PD-1 immunotherapy in advanced gastroesophageal cancer
Abstract
The addition of anti-PD-1 immunotherapy to the therapeutic armamentarium of advanced gastroesophageal (GE) cancer patients has resulted in modest improvemen...
The NLRP3 molecule influences the therapeutic effects of mesenchymal stem cells through reprogramming energy metabolism
The NLRP3 molecule influences the therapeutic effects of mesenchymal stem cells through reprogramming energy metabolism
Abstract
Background
Numerous studies have demonstrated that NLRP3 is involved in the pathogenesis of inflammatory bowel disease (IBD). Mesenchymal stem cells (MSCs) have be...
Role of endothelin and vasopressin in DOCA‐salt hypertension
Role of endothelin and vasopressin in DOCA‐salt hypertension
The relative roles of endothelin (ET) and vasopressin (AVP) in the regulation of blood pressure (BP), cardiac output (CO) and total peripheral resistance (TPR) were investigated in...
[RETRACTED] Gro-X Male Enhancement | Safely Grow Your Size, Sex Drive v1
[RETRACTED] Gro-X Male Enhancement | Safely Grow Your Size, Sex Drive v1
[RETRACTED]Gro-X Male Enhancement Reviews - Is It Worth the Money? Scam or Legit? Gro-X Male Enhancement Male health is very important, especially for a couple. Low sperm count an...

