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Substance P-like immunoreactivity in the parietal eye visual system of the lizard Uta stansburiana

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Summary

We examined the parietal eye visual system of the iguanid lizard Uta stansburiana for the presence of substance P-like immunoreactivity by use of both immunofluorescence and peroxidase-antiperoxidase techniques. In the parietal eye no substance P-containing somata were found; however, its plexiform layer contained small (ca. 1 μm diam) immunoreactive fibers. These fibers apparently originate outside the parietal eye. Immunoreactive fibers also were found in the parietal nerve, the dorsal sac, and the leptomeninx of the pineal gland. No labeled somata were observed in any of these regions in either normal or colchicine treated animals. Previously we demonstrated that a system of centrifugal fibers to the parietal eye originates from neurons in the dorsal sac (Engbretson et al. 1981). The apparent absence of substance P-containing neurons in the dorsal sac suggests that the substance P-containing fibers in the parietal eye are not the previously observed centrifugal fibers. The source of the substance P-containing fibers in the parietal eye is unknown. The pars dorsolateralis of the left medial habenular nucleus receives a dense substance P-positive projection. No such projection was seen in the right habenula. Simultaneous visualization of the terminals of ganglion cells of the parietal eye (labeled with orthograde intraaxonally transported horseradish peroxidase) and substance P-like immunofluorescence showed that the locus of habenular immunoreactivity is distinct from the projection field of the parietal eye. Thus the substance P-positive terminals in the habenula do not originate in the parietal eye. Transection of the parietal nerve confirmed this conclusion.

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References

  • Ariëns-Kappers CU, Huber GC, Crosby EC (1936) The comparative anatomy of the nervous system of vertebrates including man. Macmillan, New York

    Google Scholar 

  • Brecha N, Karten HJ, Laverack C (1979) Enkephalin-containing amacrine cells in the avian retina: immunohistochemical localization. Proc Natl Acad Sci USA 76:3010–3014

    Google Scholar 

  • Brecha N, Karten HJ, Schenker C (1981) Neurotensin-like and somatostatin-like immunoreactivity within amacrine cells of the retina. Neuroscience 6:1329–1340

    Google Scholar 

  • Collin JP (1979) Recent advances in pineal cytochemistry. Evidence of the production of indoleamines and proteinaceous substances by rudimentary photoreceptor cells and pinealocytes of amniota. Prog in Brain Res 52:271–296

    Google Scholar 

  • Cuello AC, Kanazawa J (1978) The distribution of substance P immunoreactive fibers in the rat central nervous system. J Comp Neurol 178:129–146

    Google Scholar 

  • Cuello AC, Galfre G, Milstein C (1979) Detection of substance P in the central nervous system by a monoclonal antibody. Proc Natl Acad Sci USA 76:3532–3536

    Google Scholar 

  • Eakin RM (1964) Development of the third eye in the lizard, Sceloporus occidentalis. Rev Suisse Zool 71:267–285

    Google Scholar 

  • Eakin RM, Westfall JA (1960) Further observations on the fine structure of the parietal eye of lizards. J Biophys Biochem Cytol 8:483–499

    Google Scholar 

  • Edvinsson L, McCulloch J, Uddman R (1981) SubstanceP: immunohistochemical localization and effect upon cat pial arteries in vitro and in situ. J Physiol 318:251–258

    Google Scholar 

  • Engbretson GA, Lent CM (1976) Parietal eye of the lizard: neuronal photoresponses and feedback from the pineal gland. Proc Natl Acad Sci USA 73:654–657

    Google Scholar 

  • Engbretson GA, Reiner A, Brecha N (1981) Habenular asymmetry and the central connections of the parietal eye of the lizard. J Comp Neurol 198:155–165

    Google Scholar 

  • Herkenham M, Nauta WJH (1977) Afferent connections of the habenular nuclei in the rat. A horseradish peroxidase study, with a note on the fiber-of-passage problem. J Comp Neurol 173:123–145

    Google Scholar 

  • Hökfelt T, Kellerth JD, Nilsson G, Pernow B (1974) Substance P: localization in the central nervous system and in some primary sensory neurons. Science 190:889–890

    Google Scholar 

  • Iversen LL, Nicoll RA, Vale WW (eds) (1978) Neurobiology of peptides. Neurosci Res Prog Bull 16:211–370

  • Jenison G, Nolte J (1979) The fine structure of the parietal retinas of Anolis carolinensis and Iguana iguana. Cell Tissue Res 199:235–247

    Google Scholar 

  • Karten HJ, Brecha N (1980) Localisation of substance P immunoreactivity in amacrine cells of the retina. Nature 283:87–88

    Google Scholar 

  • Korf H-W, Wagner U (1981) Nervous connections of the parietal eye in adult Lacerta s. sicula Rafinesque as demonstrated by anterograde and retrograde transport of horseradish peroxidase. Cell Tissue Res 219:567–583

    Google Scholar 

  • Kreutzberg GW (1969) Neural dynamics and axonal flow. 4. Blockage of intra-axonal enzyme transport by colchicine. Proc Natl Acad Sci USA 62:722–728

    Google Scholar 

  • LaVail JH, LaVail MM (1974) The retrograde intraaxonal transport of horseradish peroxidase in the chick visual system: a light and electron microscopic study. J Comp Neurol 157:303–358

    Google Scholar 

  • Ljungdahl A, Hökfelt T, Nilsson G (1978) Distribution of substance P-like immunoreactivity in the central nervous system of the rat. I. Cell bodies and terminals. Neuroscience 3:861–943

    Article  CAS  PubMed  Google Scholar 

  • Meiniel A, Collin JP, Hartwig HG (1973) Pinéal et troisième oeil de Lacerta vivipara (J.), au cours de la vie embryonnaire et postnatale. Z Zellforsch 144:89–115

    Google Scholar 

  • Meiniel A, Collin JP, Roux M (1975) Pinéal et 3ème oeil de l'embryon de Lacerta vivipara: étude qualitative et quantitative, en microscopie photonique de l'incorporation de 5-hydroxytryptophane-3H au cours de l'ontogenèse. J Neural Transm 36:249–279

    Google Scholar 

  • Mroz EA, Brownstein MJ, Leeman SE (1976) Evidence for substance P in the habenularinterpeduncular tract. Brain Res 113:597–599

    Google Scholar 

  • Petit A (1968) Ultrastructure de la rétine de l'oeil pariétal d'un Lacertilien, Anguis fragilis. Z Zellforsch 92:70–93

    Google Scholar 

  • Quay WB (1965) Retinal and pineal hydroxyindole-O-methyl transferase activity in vertebrates. Life Sci 4:983–991

    Google Scholar 

  • Quay WB (1979) The parietal eye-pineal complex. In: Gans C, Northcutt RG, Ulinski P (eds) Biology of the reptilia Vol 9A. Academic Press, New York

    Google Scholar 

  • Reiner A, Karten HJ, Korte G (1980) Substance P: localization within paleostriato-tegmental pathways in birds and reptiles. Soc Neurosci Abstr 6:810

    Google Scholar 

  • Stebbins RC (1954) Amphibians and reptiles of Western North America. McGraw-Hill, New York

    Google Scholar 

  • Sternberger LA (1979) Immunocytochemistry. John Wiley and Sons, New York, 2nd ed

    Google Scholar 

  • Watson JT (1979) Autoradiographic evidence of central connections of the parietal nerve in the lizard Holbrookia propinqua. Brain Res 178:577–579

    Google Scholar 

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Engbretson, G.A., Brecha, N. & Reiner, A. Substance P-like immunoreactivity in the parietal eye visual system of the lizard Uta stansburiana . Cell Tissue Res. 227, 543–554 (1982). https://doi.org/10.1007/BF00204784

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