Elsevier

Bone

Volume 19, Issue 6, December 1996, Pages 609-614
Bone

Original article
Involvement of different ion channels in osteoblasts' and osteocytes' early responses to mechanical strain

https://doi.org/10.1016/S8756-3282(96)00260-8Get rights and content

Abstract

The involvement of functional ion channels in previously documented early responses of osteocytes and osteoblasts to mechanical strain in bone tissue was investigated in explants of rat ulnae by the use of ion channel blockers. Gadolinium chloride (a blocker of stretch/shear-sensitive cation channels) elevated basal prostaglandin (PG) E2 and prostacyclin (PGI2) release and osteocyte glucose-6-phosphate dehydrogenase (G6PD) activity, but was associated with a reduction in basal nitric oxide (NO) production. Gadolinium abolished loading-related increases in the release of PGI2 and NO and osteocyte G6PD activity. Gadolinium also reduced the loading-related release of PGE2 assumed to originate from osteoblasts and the magnitude of loading-related increases in G6PD activity in these cells. Nifedipine (a blocker of L-type voltage-dependent calcium channels) had no effect on basal levels of prostanoid or NO release, or G6PD activity in osteocytes or osteoblasts, and did not affect loading-related release of PGI2 or increase in osteocyte G6PD. However, nifedipine prevented loading-related increases in PGE2 and NO release and osteoblast G6PD activity. These results are consistent with osteocytes' response to bone loading requiring activatable ion channels sensitive to gadolinium, but not those sensitive to nifedipine. In osteoblasts, the early responses to bone loading appear to be associated with ion channels sensitive to gadolinium and nifedipine; however, the nifedipine-sensitive channels seem to have the dominant effect.

References (45)

  • S.L. Dallas et al.

    Early strain-related changes in cultured embryonic chick tibiotarsi parallel those associated with adaptive modeling in vivo

    J Bone Miner Res

    (1993)
  • R.M. Davidson et al.

    Multiple forms of mechanosensitive ion channels in osteoblast-like cells

    Pflugers Arch

    (1990)
  • M.J. Davis et al.

    Stretch-activated single-channel and whole cell currents in vascular smooth muscle cells

    Am J Physiol

    (1992)
  • A.J. El-Haj et al.

    Cellular responses to mechanical loading in vitro

    J Bone Miner Res

    (1990)
  • J. Ferrante et al.

    Drug- and disease induced regulation of voltage-dependent calcium channels

    Pharm Rev

    (1990)
  • S.W. Fox et al.

    Nitric oxide is an early mediator of the induction of bone formation by mechanical strain

    J Bone Miner Res

    (1995)
  • M. Hecker et al.

    Vasoconstriction and increased flow: Two principal mechanisms of shear stress-dependent endothelial autocoid release

    Am J Physiol

    (1993)
  • W.S.S. Jee et al.

    The role of bone cells in increasing metaphyseal hard tissue in rapidly growing rats treated with prostaglandin E2

    Bone

    (1987)
  • J. Klein-Nulend et al.

    Sensitivity of osteocytes to biomechanical stress in vitro

    FASEB J

    (1995)
  • H. MacArthur et al.

    Selective inhibition of agonist-induced but not shear stress dependent release of endothelial autocoids by thapsigargin

    Br J Pharmacol

    (1993)
  • J.R. Mosley

    The effect of mechanical load and oestrogen on the development of long bone architecture

    PhD thesis

    (1996)
  • D.W. Murray et al.

    The effect of strain on bone cell prostaglandin E2 release: A new experimental method

    Calcif Tissue Int

    (1990)
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