Impaired Kv7 channel activity in the central amygdala contributes to elevated sympathetic outflow in hypertension

Cardiovasc Res. 2022 Jan 29;118(2):585-596. doi: 10.1093/cvr/cvab031.

Abstract

Aims: Elevated sympathetic outflow is associated with primary hypertension. However, the mechanisms involved in heightened sympathetic outflow in hypertension are unclear. The central amygdala (CeA) regulates autonomic components of emotions through projections to the brainstem. The neuronal Kv7 channel is a non-inactivating voltage-dependent K+ channel encoded by KCNQ2/3 genes involved in stabilizing the neuronal membrane potential and regulating neuronal excitability. In this study, we investigated if altered Kv7 channel activity in the CeA contributes to heightened sympathetic outflow in hypertension.

Methods and results: The mRNA and protein expression levels of Kv7.2/Kv7.3 in the CeA were significantly reduced in spontaneously hypertensive rats (SHRs) compared with Wistar-Kyoto (WKY) rats. Lowering blood pressure with coeliac ganglionectomy in SHRs did not alter Kv7.2 and Kv7.3 channel expression levels in the CeA. Fluospheres were injected into the rostral ventrolateral medulla (RVLM) to retrogradely label CeA neurons projecting to the RVLM (CeA-RVLM neurons). Kv7 channel currents recorded from CeA-RVLM neurons in brain slices were much smaller in SHRs than in WKY rats. Furthermore, the basal firing activity of CeA-RVLM neurons was significantly greater in SHRs than in WKY rats. Bath application of specific Kv7 channel blocker 10, 10-bis (4-pyridinylmethyl)-9(10H)-anthracnose (XE-991) increased the excitability of CeA-RVLM neurons in WKY rats, but not in SHRs. Microinjection of XE-991 into the CeA increased arterial blood pressure (ABP) and renal sympathetic nerve activity (RSNA), while microinjection of Kv7 channel opener QO-58 decreased ABP and RSNA, in anaesthetized WKY rats but not SHRs.

Conclusions: Our findings suggest that diminished Kv7 channel activity in the CeA contributes to elevated sympathetic outflow in primary hypertension. This novel information provides new mechanistic insight into the pathogenesis of neurogenic hypertension.

Keywords: Autonomic nervous system; Central amygdala; Hypertension; Potassium channel; Sympathetic nervous system.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Arterial Pressure*
  • Central Amygdaloid Nucleus / metabolism*
  • Central Amygdaloid Nucleus / physiopathology
  • Disease Models, Animal
  • Hypertension / genetics
  • Hypertension / metabolism*
  • Hypertension / physiopathology
  • KCNQ2 Potassium Channel / genetics
  • KCNQ2 Potassium Channel / metabolism*
  • KCNQ3 Potassium Channel / genetics
  • KCNQ3 Potassium Channel / metabolism*
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Male
  • Medulla Oblongata / metabolism*
  • Medulla Oblongata / physiopathology
  • Membrane Potentials
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neuroanatomical Tract-Tracing Techniques
  • Neurons / metabolism
  • Potassium / metabolism*
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred WKY
  • Red Fluorescent Protein
  • Signal Transduction
  • Sympathetic Nervous System / physiopathology*
  • Vesicular Glutamate Transport Protein 2 / genetics

Substances

  • KCNQ2 Potassium Channel
  • KCNQ3 Potassium Channel
  • Kcnq2 protein, rat
  • Kcnq3 protein, rat
  • Luminescent Proteins
  • Vesicular Glutamate Transport Protein 2
  • Potassium