April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Lamina cribrosa pore size increases when human eyes are subjected to acute intraocular pressure elevation
Author Affiliations & Notes
  • Rouzbeh Amini
    Biomedical Engineering, University of Akron, Akron, OH
  • Jonathan L Grimm
    Ophthalmology, University of Pittsburgh, Pittsburgh, PA
  • Ning-Jiun Jan
    Ophthalmology, University of Pittsburgh, Pittsburgh, PA
    Bioengineering, University of Pittsburgh, Pittsburgh, PA
  • Donald J Brown
    Gavin Herbert Eye Institute, University of California, Irvine, Irvine, CA
  • Ian A Sigal
    Ophthalmology, University of Pittsburgh, Pittsburgh, PA
    Bioengineering, University of Pittsburgh, Pittsburgh, PA
  • Footnotes
    Commercial Relationships Rouzbeh Amini, None; Jonathan Grimm, None; Ning-Jiun Jan, None; Donald Brown, None; Ian Sigal, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 4249. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Rouzbeh Amini, Jonathan L Grimm, Ning-Jiun Jan, Donald J Brown, Ian A Sigal; Lamina cribrosa pore size increases when human eyes are subjected to acute intraocular pressure elevation. Invest. Ophthalmol. Vis. Sci. 2014;55(13):4249.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract
 
Purpose
 

To quantify eye-specific areal, circumferential, and radial stretches induced within the lamina cribrosa (LC) and pia matter of human eyes subjected to acute intraocular pressure (IOP) elevation.

 
Methods
 

Five human eyes from three donors aged 23-82 were scanned using second harmonic generated (SHG) imaging (Zeiss 510 Meta LSM). The optic nerves were cut to allow imaging of the LC from the posterior direction. Images up to a depth of 300 µm (2 µm depth resolution) were acquired at IOPs ranging from 10 to 50 mmHg, after allowing equilibration for 30 min. Mosaic lateral resolution varied from1.76 to 4.97 µm/pixel. Digital image correlation techniques were used to calculate the deformation mapping between maximum intensity projection images at low and at elevated IOP (Sigal IA, et al. IOVS 2013; In-Press). The LC beams, LC pores, and pia matter were segmented manually. Stretches were calculated for each segmented section separately.

 
Results
 

In all samples the LC pores areal stretch increased significantly when IOP was elevated (P’s< 0.0001, single-tailed t-test for each sample, Figure). In the pia region, in all but one case, the circumferential stretch was significantly higher than the radial stretch (P’s < 0.0001, single-tailed paired t-test). Further, in all but one case, the value of both circumferential and radial stretches was significantly higher than one (P’s< 0.0001, single-tailed t-test for each sample). Although the standard deviations of the measured values were relatively small, there were regional differences in the stretch values of the LC pores, LC beams, and pia matters of the eyes (Figure).

 
Conclusions
 

We measured eye-specific IOP-induced directional deformations of the pores and beams of the LC as well as those of pia matter in uncut and unfixed human eyes. The most interesting outcome was the increase in the average area of the LC pores during exposure to high IOP. Thus, for the majority of the retinal ganglion cell axons, the passage through the LC expanded. Only for a small minority of the axons did the physical space for passing the LC narrowed. In the pia region, as expected, the direction of higher stretch (i.e. circumferential direction) matched the gross ECM structure. Such matching further exemplifies how in numerous regions of the ocular globe (e.g. pia, corneal limbus, etc.), the tissue structure anisotropy is closely related to its mechanical function.

  
Keywords: 577 lamina cribrosa • 629 optic nerve • 708 sclera  
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×