HB-EGF depolarizes hippocampal arterioles to restore myogenic tone in a genetic model of small vessel disease

Mech Ageing Dev. 2020 Dec:192:111389. doi: 10.1016/j.mad.2020.111389. Epub 2020 Oct 27.

Abstract

Vascular cognitive impairment, the second most common cause of dementia, profoundly affects hippocampal-dependent functions. However, while the growing literature covers complex neuronal interactions, little is known about the sustaining hippocampal microcirculation. Here we examined vasoconstriction to physiological pressures of hippocampal arterioles, a fundamental feature of small arteries, in a genetic mouse model of CADASIL, an archetypal cerebral small vessel disease. Using diameter and membrane potential recordings on isolated arterioles, we observed both blunted pressure-induced vasoconstriction and smooth muscle cell depolarization in CADASIL. This impairment was abolished in the presence of voltage-gated potassium (KV1) channel blocker 4-aminopyridine, or by application of heparin-binding EGF-like growth factor (HB-EGF), which promotes KV1 channel down-regulations. Interestingly, we observed that HB-EGF induced a depolarization of the myocyte plasma membrane within the arteriolar wall in CADASIL, but not wild-type, arterioles. Collectively, our results indicate that hippocampal arterioles in CADASIL mice display a blunted contractile response to luminal pressure, similar to the defect we previously reported in cortical arterioles and pial arteries, that is rescued by HB-EGF. Hippocampal vascular dysfunction in CADASIL could then contribute to the decreased vascular reserve associated with decreased cognitive performance, and its correction may provide a therapeutic option for treating vascular cognitive impairment.

Keywords: CADASIL; Cerebral small vessel disease; Epidermal growth factor receptor; Heparin-binding EGF-like growth factor; Hippocampus; K(V)1 channel; Microcirculation; Potassium channel; Vascular cognitive impairment.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminopyridines / pharmacology
  • Animals
  • Arterioles* / metabolism
  • Arterioles* / physiopathology
  • Cerebral Small Vessel Diseases / metabolism
  • Cerebral Small Vessel Diseases / physiopathology
  • Dementia, Vascular / metabolism
  • Dementia, Vascular / physiopathology
  • Heparin-binding EGF-like Growth Factor / metabolism*
  • Hippocampus* / blood supply
  • Hippocampus* / metabolism
  • Membrane Potentials / physiology
  • Membrane Transport Modulators / pharmacology
  • Mice
  • Microcirculation
  • Models, Genetic
  • Muscle, Smooth, Vascular / metabolism
  • Myocytes, Smooth Muscle / metabolism
  • Potassium Channels, Voltage-Gated / antagonists & inhibitors*
  • Vasoconstriction / drug effects
  • Vasoconstriction / physiology

Substances

  • Aminopyridines
  • Heparin-binding EGF-like Growth Factor
  • Membrane Transport Modulators
  • Potassium Channels, Voltage-Gated