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Inhibition of mTORC2 promotes natriuresis in Dahl salt-sensitive rats via the decrease of NCC and ENaC activity
Chun Yang1, Elena Isaeva2, Satoshi Shimada1
1Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin, United States.
Abstract:
We have previously observed that prolonged administration of rapamycin, an inhibitor targeting the mammalian target of rapamycin complex (mTORC)1, partially reduced hypertension and alleviated kidney inflammation in Dahl salt-sensitive (SS) rats. In contrast, treatment with PP242, an inhibitor affecting both mTORC1/mTORC2, not only completely prevented hypertension but also provided substantial protection against kidney injury. Notably, PP242 exhibited potent natriuretic effects that were not evident with rapamycin. The primary objective of this study was to pinpoint the specific tubular sites responsible for the natriuretic effect of PP242 in SS rats subjected to either 0.4% NaCl (normal salt) or 4.0% NaCl (high salt) diet. Acute effects of PP242 on natriuretic, diuretic, and kaliuretic responses were determined in unanesthetized SS rats utilizing benzamil, furosemide, or hydrochlorothiazide [inhibitors of epithelial Na+ channel (ENaC), Na-K-2Cl cotransporter (NKCC2), or Na-Cl cotransporter (NCC), respectively] either administered alone or in combination. The findings indicate that the natriuretic effects of PP242 in SS rats stem predominantly from the inhibition of NCC and a reduction of ENaC open probability. Molecular analysis revealed that mTORC2 regulates NCC activity through protein phosphorylation and ENaC activity through proteolytic cleavage in vivo. Evidence also indicated that PP242 also prevents the loss of K+ associated with the inhibition of NCC. These findings suggest that PP242 may represent an improved therapeutic approach for antihypertensive intervention, potentially controlling blood pressure and mitigating kidney injury in salt-sensitive human subjects.NEW & NOTEWORTHY This study explored mechanisms underlying the natriuretic effects of mammalian target of rapamycin protein complex 2 inhibition using PP242 and revealed both epithelial Na+ channel and Na-Cl cotransporter in the distal tubular segments were potentially inhibited. These observations, with prior lab evidence, indicate that PP242 prevents hypertension via its potent inhibitory effects on these specific sodium transporters and by reducing renal immune responses. This dual action, coupled with potassium sparing effects, suggests an improved approach for managing hypertension and associated kidney damage.
Insights
PP242, an mTORC inhibitor, effectively lowers blood pressure and protects kidneys in salt-sensitive rats by inhibiting NCC and ENaC transporters. This dual action offers a promising therapeutic strategy for hypertension and kidney damage.
Area of Science:
- Nephrology and Hypertension Research
- Molecular Pharmacology of Kidney Transporters
- Mammalian Target of Rapamycin (mTOR) Signaling Pathways
Background:
- Previous studies showed rapamycin partially reduced hypertension and kidney inflammation in Dahl salt-sensitive (SS) rats.
- PP242, a dual mTORC1/mTORC2 inhibitor, completely prevented hypertension and protected against kidney injury in SS rats.
- PP242 demonstrated potent natriuretic effects, unlike rapamycin.
Purpose of the Study:
- To identify the specific renal tubular sites responsible for the natriuretic effect of PP242 in SS rats.
- To elucidate the molecular mechanisms by which PP242 exerts its antihypertensive and renoprotective effects.
Main Methods:
- Acute administration of PP242 in unanesthetized SS rats on normal or high salt diets.
- Assessment of natriuretic, diuretic, and kaliuretic responses using specific inhibitors: benzamil (ENaC), furosemide (NKCC2), and hydrochlorothiazide (NCC).
- Molecular analysis to investigate mTORC2 regulation of NCC and ENaC activity.
Main Results:
- PP242's natriuretic effects in SS rats are primarily due to the inhibition of the Na-Cl cotransporter (NCC) and reduced epithelial Na+ channel (ENaC) open probability.
- Molecular data indicate mTORC2 regulates NCC activity via phosphorylation and ENaC activity via proteolytic cleavage.
- PP242 prevented potassium loss associated with NCC inhibition, suggesting a potassium-sparing effect.
Conclusions:
- PP242 inhibits NCC and reduces ENaC activity in distal tubular segments, leading to significant natriuresis and antihypertensive effects.
- mTORC2 plays a crucial role in regulating NCC and ENaC function in vivo.
- PP242 presents a potential improved therapeutic strategy for managing hypertension and kidney injury in salt-sensitive individuals due to its dual action on sodium transporters and potential potassium-sparing properties.
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