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Downregulation of Renal G Protein – Coupled Receptor Kinase Type 4 Expression via Ultrasound ‐ Targeted Microbubble Destruction Lowers Blood Pressure in Spontaneously Hypertensive Rats

View Article: PubMed Central - PubMed

ABSTRACT

Background: G protein–coupled receptor kinase type 4 (GRK4) plays a vital role in the long‐term control of blood pressure (BP) and sodium excretion by regulating renal G protein–coupled receptor phosphorylation, including dopamine type 1 receptor (D1R). Ultrasound‐targeted microbubble destruction (UTMD) is a promising method for gene delivery. Whether this method can deliver GRK4 small interfering RNA (siRNA) and lower BP is not known.

Methods and results: BP, 24‐hour sodium excretion, and urine volume were measured after UTMD‐targeted GRK4 siRNA delivery to the kidney in spontaneously hypertensive rats. The expression levels of GRK4 and D1R were determined by immunoblotting. The phosphorylation of D1R was investigated using immunoprecipitation. The present study revealed that UTMD‐mediated renal GRK4 siRNA delivery efficiently reduced GRK4 expression and lowered BP in spontaneously hypertensive rats, accompanied by increased sodium excretion. The increased sodium excretion might be accounted for by the UTMD regulation of D1R phosphorylation and function in spontaneously hypertensive rats. Further analysis showed that, although UTMD had no effect on D1R expression, it reduced D1R phosphorylation in spontaneously hypertensive rats kidneys and consequently increased D1R‐mediated natriuresis and diuresis.

Conclusions: Taken together, these study results indicate that UTMD‐targeted GRK4 siRNA delivery to the kidney effectively reduces D1R phosphorylation by inhibiting renal GRK4 expression, improving D1R‐mediated natriuresis and diuresis, and lowering BP, which may provide a promising novel strategy for gene therapy for hypertension.

No MeSH data available.


Effects of ultrasound‐targeted microbubble destruction (UTMD)–mediated G protein–coupled receptor kinase type 4 (GRK4) small interfering RNA delivery on blood pressure. UTMD‐mediated GRK4 small interfering RNA delivery decreased systolic blood pressure (SBP) (A) and mean arterial pressure (MAP) (B) in spontaneously hypertensive rats (n=5, *P<0.05 vs control).
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jah31805-fig-0004: Effects of ultrasound‐targeted microbubble destruction (UTMD)–mediated G protein–coupled receptor kinase type 4 (GRK4) small interfering RNA delivery on blood pressure. UTMD‐mediated GRK4 small interfering RNA delivery decreased systolic blood pressure (SBP) (A) and mean arterial pressure (MAP) (B) in spontaneously hypertensive rats (n=5, *P<0.05 vs control).

Mentions: Owing to the importance of GRK4 on BP regulation, we also checked BP in those rats. The results revealed that the basal BP was comparable between the UTMD treatment group and the control group. A significant difference was found from 12 days after UTMD treatment and was maintained for at least 20 days (Figure 4A and 4B). Our further study also revealed that GRK4 siRNA via UTMD increased the 24‐hour sodium excretion and urine volume from 12 days (Figure 5A and 5B).


Downregulation of Renal G Protein – Coupled Receptor Kinase Type 4 Expression via Ultrasound ‐ Targeted Microbubble Destruction Lowers Blood Pressure in Spontaneously Hypertensive Rats
Effects of ultrasound‐targeted microbubble destruction (UTMD)–mediated G protein–coupled receptor kinase type 4 (GRK4) small interfering RNA delivery on blood pressure. UTMD‐mediated GRK4 small interfering RNA delivery decreased systolic blood pressure (SBP) (A) and mean arterial pressure (MAP) (B) in spontaneously hypertensive rats (n=5, *P<0.05 vs control).
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Related In: Results  -  Collection

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jah31805-fig-0004: Effects of ultrasound‐targeted microbubble destruction (UTMD)–mediated G protein–coupled receptor kinase type 4 (GRK4) small interfering RNA delivery on blood pressure. UTMD‐mediated GRK4 small interfering RNA delivery decreased systolic blood pressure (SBP) (A) and mean arterial pressure (MAP) (B) in spontaneously hypertensive rats (n=5, *P<0.05 vs control).
Mentions: Owing to the importance of GRK4 on BP regulation, we also checked BP in those rats. The results revealed that the basal BP was comparable between the UTMD treatment group and the control group. A significant difference was found from 12 days after UTMD treatment and was maintained for at least 20 days (Figure 4A and 4B). Our further study also revealed that GRK4 siRNA via UTMD increased the 24‐hour sodium excretion and urine volume from 12 days (Figure 5A and 5B).

View Article: PubMed Central - PubMed

ABSTRACT

Background: G protein&ndash;coupled receptor kinase type 4 (GRK4) plays a vital role in the long&#8208;term control of blood pressure (BP) and sodium excretion by regulating renal G protein&ndash;coupled receptor phosphorylation, including dopamine type 1 receptor (D1R). Ultrasound&#8208;targeted microbubble destruction (UTMD) is a promising method for gene delivery. Whether this method can deliver GRK4 small interfering RNA (siRNA) and lower BP is not known.

Methods and results: BP, 24&#8208;hour sodium excretion, and urine volume were measured after UTMD&#8208;targeted GRK4 siRNA delivery to the kidney in spontaneously hypertensive rats. The expression levels of GRK4 and D1R were determined by immunoblotting. The phosphorylation of D1R was investigated using immunoprecipitation. The present study revealed that UTMD&#8208;mediated renal GRK4 siRNA delivery efficiently reduced GRK4 expression and lowered BP in spontaneously hypertensive rats, accompanied by increased sodium excretion. The increased sodium excretion might be accounted for by the UTMD regulation of D1R phosphorylation and function in spontaneously hypertensive rats. Further analysis showed that, although UTMD had no effect on D1R expression, it reduced D1R phosphorylation in spontaneously hypertensive rats kidneys and consequently increased D1R&#8208;mediated natriuresis and diuresis.

Conclusions: Taken together, these study results indicate that UTMD&#8208;targeted GRK4 siRNA delivery to the kidney effectively reduces D1R phosphorylation by inhibiting renal GRK4 expression, improving D1R&#8208;mediated natriuresis and diuresis, and lowering BP, which may provide a promising novel strategy for gene therapy for hypertension.

No MeSH data available.