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Breed- and gender-dependent differences in eye growth and form deprivation responses in chick

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Abstract

This study investigated the influences of breed and gender on the response to form deprivation and subsequent changes (recovery) when normal vision was restored. Two breeds of chickens, the White Leghorn and broiler cross, were compared, as well as male and female chicks for the White Leghorn breed. Normal eye growth was faster in the more rapidly growing broiler chicks; gender-differences were not as great as breed-differences although male White Leghorns ultimately became heavier and showed slightly greater normal eye growth than females. While both breeds showed high myopia and axial elongation in response to form deprivation, they differed significantly in the magnitude of their response, with White Leghorns showing more myopia and greater axial elongation and also recovering more slowly. Responses to form deprivation were similar for both genders, with respect to both the amount of myopia and axial elongation produced, although the female chicks recovered faster. Together these observations indicate that, although the overall pattern of response of form deprivation is consistent across both breed and gender, related quantitative differences in responses can be expected and need to be taken into account in experimental design and cross-study comparisons.

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Abbreviations

WL :

White Leghorn chicks

BC :

broiler cross chicks

M :

male chicks

F :

female chicks

N :

normal eye

T :

treated eye

FD :

form deprivation

ACD :

anterior chamber depth

ALT :

axial lens thickness

VCD :

vitreous chamber depth

AL :

axial length

References

  • Adret P, Rogers LJ (1989) Sex difference in the visual projections of young chicks: A quantitative study of the thalamofugal pathway. Brain Res 478: 59–73

    Google Scholar 

  • Bartmann M, Schaeffel F (1994) A simple mechanism for emmetropization without cues from accommodation or colour. Vision Res 34: 873–876

    Google Scholar 

  • Bartmann M, Schaeffel F, Hagel G, Zrenner E (1994) Constant light affects retinal dopamine levels and blocks deprivation myopia but not lens-induced refractive errors in chickens. Visual Neurosci 11: 199–208

    Google Scholar 

  • Bercovitz AB, Harrison PC, Leary GA (1972) Light induced alterations in growth pattern of the avian eye. Vision Res 12: 1253–1259

    Google Scholar 

  • Bradshaw JL, Rogers LJ (1993) The evolution of lateral asymmetries, language, tool use, and intellect. Chapter 2. Asymmetries in birds. Academic Press, San Diego, pp 37–97

    Google Scholar 

  • Goldschmidt E (1969) Refraction in the newborn. Acta Ophthalmol 47: 570–577

    Google Scholar 

  • Goss DA (1987) Cessation of the age of childhood myopia progression. Ophthalmol Physiol Opt 7: 195–197

    Google Scholar 

  • Goss DA, Winkler RL (1983) Progression of myopia in youth: Age of cessation. Am J Optom Physiol Opt 60: 651–658

    Google Scholar 

  • Grosvenor T (1988) Myopia in Melanesian school children in Vanuatu. Acta Ophthalmol (Suppl) 185: 24–28

    Google Scholar 

  • Hayes BP, Fitzke FW, Hodos W, Holden AL (1986) A morphological analysis of experimental myopia in young chicks. Invest Ophthalmol Vis Sci 27: 981–991

    Google Scholar 

  • Johnson RJ (1988) Diminution of pulsatile growth hormone secretion in the domestic fowl (Gallus domesticus): Evidence of sexual dimorphism. J Endocrinol 199: 101–109

    Google Scholar 

  • Larsen JS (1971a) The sagittal growth of the eye. III. Ultrasonic measurement of the posterior segment (axial length of the vitreous) from birth to puberty. Acta Ophthalmol 49: 441–453

    Google Scholar 

  • Larsen JS (1971b) The sagittal growth of the eye. IV. Ultrasonic measurement of the axial length of the eye from birth to puberty. Acta Ophthalmol 49: 873–886

    Google Scholar 

  • Lauber JK, Kinnear A (1979) Eye enlargement in birds induced by dim light. Can J Ophthalmol 14: 265–269

    Google Scholar 

  • Lauber JK, Oishi T (1987) Lid suture myopia in chicks. Invest Ophthalmol Vis Sci 28: 1851–1858

    Google Scholar 

  • Lin LL, Chen C, Hung P, Ko L (1988) Nation-wide survey of myopia among schoolchildren in Taiwan, 1986. Acta Ophlhalmol (Suppl) 185: 29–34

    Google Scholar 

  • Mench JA, Andrew RJ (1986) Lateralization of a food search task in the domestic chick. Behav Neur Biol 46: 107–114

    Google Scholar 

  • Norton TT (1990) Experimental myopia in tree shrews. In: Bock G, Widdows K (eds) Myopia and the control of eye growth. Ciba Foundation Symposium 155. John Wiley and Sons Ltd, Chichester, pp 178–199

    Google Scholar 

  • Osol G, Schwartz B, Foss DC (1986) The effect of photoperiod and lid suture on eye growth in chickens. Invest Ophthalmol Vis Sci 27: 255–260

    Google Scholar 

  • Pickett-Seltner RL, Sivak JG, Pasternak JJ (1988) Experimentally induced myopia in chicks: Morphometric and biochemical analysis during the first 14 days after hatching. Vision Res 28: 323–328

    Google Scholar 

  • Rada J, McFarland AL, Cornuet P, Hassell J (1992) Increased aggrecan (cartilage proteoglycan) production in the sclera of myopic chicks. Dev Biol 147: 303–312

    Google Scholar 

  • Rajendra S, Rogers LJ (1993) Asymmetry is present in the thalamofugal visual projections of female chicks. Exp Brain Res 92: 542–544

    Google Scholar 

  • Raviola E, Wiesel TN (1990) Neural control of eye growth and experimental myopia in primates. In: Bock G, Widdows K (eds) Myopia and the control of eye growth. Ciba Foundation Symposium 155. John Wiley and Sons Ltd, Chichester, pp 22–44

    Google Scholar 

  • Rogers LJ (1982) Light experience and asymmetry of brain function in chickens. Nature 297: 223–225

    Google Scholar 

  • Schaeffel F, Glasser A, Howland HC (1988) Accommodation, refractive error and eye growth in chickens. Vision Res 28: 639–657

    Google Scholar 

  • Schmid KL, Wildsoet CF, Pettigrew JD (1991) Myopia production and eye growth regulation in two breeds of chickens. Clin Exp Optom 74: 217

    Google Scholar 

  • Sivak JG, Barrie DL, Weerheim JA (1989) Bilateral experimental myopia in chicks. Optom Vis Sci 66: 854–858

    Google Scholar 

  • Sperduto RD, Seigel D, Roberts J, Rowland M (1983) Prevalence of myopia in the United States. Arch Ophthalmol 101: 405–407

    Google Scholar 

  • Troilo D, Gottlieb MD, Wallman J (1987) Visual deprivation causes myopia in chicks with optic nerve section. Curr Eye Res 6: 993–999

    Google Scholar 

  • Troilo D, Li T, Glasser A, Howland HC (1995) Differences in eye growth and the response to visual deprivation in different strains of chicks. Vision Res 35: 1211–1216

    Google Scholar 

  • van Rens GHMB, Arkell SM (1991) Refractive errors and axial length among Alaskan Eskimos. Acta Ophthalmol 69: 27–32

    Google Scholar 

  • Wallman J (1993) Retinal control of eye growth and refraction. In: Osbourne N, Chader G (eds) Progress in retinal research. Vol 12. Pergamon Press, Oxford, pp 133–153

    Google Scholar 

  • Wallman J, Adams JI (1987) Developmental aspects of experimental myopia in chicks: Susceptibility, recovery and relation to emmetropization. Vision Res 27: 1139–1163

    Google Scholar 

  • Wallman J, Turkel J, Trachtman JN (1978) Extreme myopia produced by modest changes in early visual experience. Science 201: 1249–1251

    Google Scholar 

  • Wallman J, Gottlieb MD, Rajaram V, Fugate-Wentzek LA (1987) Local retinal regions control local eye growth and myopia. Science 237: 73–77

    Google Scholar 

  • Wallman J, Wildsoet CF, Xu A, Gottlieb MD, Nickla DL, Marran L, Krebs W, Christensen AM (1995) Moving the retina: Choroidal modulation of refractive state. Vision Res 35: 37–50

    Google Scholar 

  • Wildsoet CF, Pettigrew JD (1988a) Experimental myopia and anomalous eye growth patterns unaffected by optic nerve section in chickens: Evidence for local control of eye growth. Clin Vis Sci 3: 99–107

    Google Scholar 

  • Wildsoet CF, Pettigrew JD (1988b) Kainic acid-induced eye enlargement in chickens: Differential effects on anterior and posterior segments. Invest Ophthalmol Vis Sci 29: 311–319

    Google Scholar 

  • Wildsoet C, Wallman J (1995) Choroidal and scleral mechanisms of compensation for spectacle lenses in chicks. Vision Res 35: 1175–1194

    Google Scholar 

  • Yinon U, Rose L, Shapiro A (1980) Myopia in the eye of developing chicks following monocular and binocular lid closure. Vision Res 20: 137–121

    Google Scholar 

  • Yinon U, Koslowe KC, Lobel D, Landshman N, Barishak YR (1982/1983) Lid suture myopia in developing chicks: Optical and structural considerations. Curr Eye Res 2: 877–882

    Google Scholar 

  • Zappia JV, Rogers LJ (1987) Sex differences and reversal of brain asymmetry by testosterone in chickens. Behav Brain Res 23: 261–267

    Google Scholar 

  • Zhu X, Lin T, Stone RA, Laties A (1994) Male and female chick eyes differ in size and responses to visual deprivation. Invest Ophthalmol Vis Sci [ARVO Suppl] 35: 1800

    Google Scholar 

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Schmid, K., Wildsoet, C. Breed- and gender-dependent differences in eye growth and form deprivation responses in chick. J Comp Physiol A 178, 551–561 (1996). https://doi.org/10.1007/BF00190185

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