Adrenergic regulation of the intracellular [Ca2+] and voltage-operated Ca2+ channel currents in the rat prostate neuroendocrine cells

Prostate. 2003 Oct 1;57(2):99-110. doi: 10.1002/pros.10277.

Abstract

Background: The prostate gland contains numerous neuroendocrine cells (PNECs) innervated by adrenergic neurons. PNECs are believed to influence the growth and physiological function of the prostate gland via paracrine release of hormones.

Materials and methods: Using fura-2 fluorescence measurement and patch-clamp techniques, we investigated the effects of adrenergic stimulation on cytosolic concentration of Ca2+ ([Ca2+]c) and high voltage-activated Ca2+ channel currents (HVA-I(Ca)) of the putative rat prostate neuroendocrine cells (RPNECs) freshly isolated by an enzymic digestion.

Results: Noradrenaline (NA, 1 microM) induced a sharp, transient increase of [Ca2+]c measured by the fura-2 fluorescence. Pharmacological studies showed that alpha1-adrenoceptors (alpha1-ARs) coupled with PLC/IP3 signaling pathway induce the release of stored Ca2+, which subsequently recruits store-operated Ca2+ entry pathways. In the whole-cell voltage clamp experiment, NA decreased the amplitude of HVA-I(Ca) by 40%, which was mimicked by an alpha2-AR agonist (UK14304) but not by an alpha1-AR agonist (phenyleprine). After selective blockade of N-type Ca2+ channels by omega-conotoxin GVIA, the addition of NA showed no further inhibition on the remaining L-type Ca2+ channel currents. The adrenergic inhibition of HVA-I(Ca) was partially prevented by the pretreatment with pertussis toxin (PTX) (5 microg/ml, 4 hr, 37 degrees C).

Conclusions: RPNECs express both alpha1- and alpha2-ARs, signaling the release of stored Ca2+ and the inhibition of N-type Ca2+ channels, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Agonists / pharmacology*
  • Animals
  • Calcium / metabolism*
  • Calcium Channels / physiology*
  • Drug Resistance
  • Electric Conductivity
  • Intracellular Fluid / metabolism*
  • Male
  • Neurosecretory Systems / cytology
  • Neurosecretory Systems / metabolism*
  • Norepinephrine / pharmacology*
  • Osmolar Concentration
  • Prostate / cytology
  • Prostate / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Adrenergic, alpha / physiology*
  • Receptors, Adrenergic, alpha-1 / physiology
  • Receptors, Adrenergic, alpha-2 / physiology
  • Sodium Channels / drug effects
  • Sodium Channels / physiology
  • Tetrodotoxin / pharmacology

Substances

  • Adrenergic alpha-Agonists
  • Calcium Channels
  • Receptors, Adrenergic, alpha
  • Receptors, Adrenergic, alpha-1
  • Receptors, Adrenergic, alpha-2
  • Sodium Channels
  • Tetrodotoxin
  • Calcium
  • Norepinephrine