Significance: Strabismus, misalignments of the visual axes, is prevalent in the US and usually treated surgically. Misdiagnoses and sub-optimal outcomes are predictable consequences of inadequate understanding of extraocular anatomy and oculomotor control. Our overall aim is to develop a quantitative, physiologically realistic understanding of extraocular biomechanics, applied to diagnosis and treatment of strabismus. We previously showed that distributed midorbital connective and smooth muscle tissues function as rectus extraocular muscle (EOM) pulley, crucial to normal ocular kinematics. Recent studies suggest that the global lamina of each EOM rotates the eye, whereas the orbital lamina translates the pulley that determines the global lamina's functional origin. More complete characterization of extraocular tissue architecture should reveal other mechanically significant structures, also not easily discriminable because distributed. These findings, and out direct physiologic muscle force measurements have cast doubt on the classic and fundamental oculomotor concept of the Final Common Path. Validation and development of these ideas will continue to have broad impact on laboratory studies of ocular motility and on diagnosis and treatment of strabismus. Studies: We will: (01) test predictions of differential contraction of global and orbital EOM laminae and movements of connective tissue pulleys with conjugate and vergence eye movements, using implanted gold microspheres and digital X-ray imaging in alert monkeys; (2) characterize extraocular tissue architecture by reconstructing multiple interlaced immunohistochemically stained thin serial sections of cadaveric human and monkey orbits; (3) test the Active Pulley Hypothesis, a challenge to the classic notion of the Final Common Path, using physiologic muscle force measurement in alert monkeys, and (4) develop scientifically and clinically useful biomechanical modeling tools that reflect current physiologic findings and hypotheses.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY013443-05
Application #
6838758
Study Section
Visual Sciences B Study Section (VISB)
Program Officer
Hunter, Chyren
Project Start
2001-01-01
Project End
2007-12-31
Budget Start
2005-01-01
Budget End
2007-12-31
Support Year
5
Fiscal Year
2005
Total Cost
$439,500
Indirect Cost
Name
Smith-Kettlewell Eye Research Institute
Department
Type
DUNS #
073121105
City
San Francisco
State
CA
Country
United States
Zip Code
94115
Miller, Joel M; Rossi, Ethan A; Wiesmair, Martin et al. (2006) Stability of gold bead tissue markers. J Vis 6:616-24
Miller, Joel M; Demer, Joseph L; Poukens, Vadims et al. (2003) Extraocular connective tissue architecture. J Vis 3:240-51
Miller, Joel (2003) No oculomotor plant, no final common path. Strabismus 11:205-11
Miller, Joel M; Bockisch, Christopher J; Pavlovski, Dmitri S (2002) Missing lateral rectus force and absence of medial rectus co-contraction in ocular convergence. J Neurophysiol 87:2421-33