Harderian Glands pp 279-295 | Cite as
The Pineal and the Harderian Glands: Evidence for Mutual Interactions
Abstract
The pineal gland and the Harderian glands have a number of biochemical and physiological features which are similar. Both organs contain melatonin and associated enzymes required for its synthesis (Cardinali and Wurtman 1972; Bubenik et al. 1978; Balemans et al. 1980; Reiter et al. 1981). Additionally, both the Harderian glands (Guerrero et al. 1987) and the pineal gland (Guerrero et al. 1988) contain the 5′-deiodinase enzyme which converts the relatively inactive thyroid hormone, thyroxine, to its active form, triiodothyronine (T3). In both the Harderian and the pineal glands, melatonin and T3 synthesis are rhythmic. Finally, both organs also exhibit day/night rhythms in vasopressin and oxytocin (Gauquelin et al. 1988). Why these organs have these similarities is unknown and, indeed, astonishing considering their widely different embryological derivations, etc. Recently, it has become apparent that there may be a bidirectional physiologic interaction between these organs. The purpose of this chapter is to summarize the presumptive interrelationships.
Keywords
Pineal Gland Syrian Hamster Melatonin Level Harderian Gland Pineal MelatoninPreview
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References
- Axelrod, Wurtman RJ, Snyder SH (1965) Control of hydrozyindole-O-methyltransferase activity in the rat pineal gland by environmental lighting. J Biol Chem 240:949–954PubMedGoogle Scholar
- Balemans MGM, Pévet P, Legerstee WC, Nevo E (1980) Preliminary investigations on melatonin and 5-methoxytryptophol synthesis in the pineal, retina and Harderian gland of the mole rat (Spalax ehrenbergi) and in the pineal of the mouse “Eyeless”. J Neural Transm 49:247–255PubMedCrossRefGoogle Scholar
- Bubenik GA, Brown GM, Grota LJ (1976) Immunohistochemical localization of melatonin in the rat Harderian gland. J Histochem Cytochem 24:1173–1177PubMedCrossRefGoogle Scholar
- Bubenik GA, Purtill RA, Brown GM, Grota LJ (1978) Melatonin in the retina and the Harderian gland. Ontogeny, diurnal variations and melatonin treatment. Exp Eye Res 27:323–333PubMedCrossRefGoogle Scholar
- Cardinali DP, Wurtman RJ (1972) Hydroxyindole-O-methyltransferase in rat pineal, retina and Harderian gland. Endocrinology 91:247–252PubMedCrossRefGoogle Scholar
- Clabough JW, Norvell JE (1974) Pineal influence on the Harderian glands of female golden hamsters. Anat Rec 178:119–125PubMedCrossRefGoogle Scholar
- Cogburn LA, Wilson-Placentra S, Letcher LR (1987) Influence of pinealectomy on plasma and extrapineal melatonin rhythms in young chickens (Gallus domesticus). Gen Comp Endocrinol 68:343–356PubMedCrossRefGoogle Scholar
- Gauquelin G, Gharib C, Ghaemmaghami F, Allevard A-M, Cherbal F, Geelen G, Bouzeghrane F, Legros J-J (1988) A day/night rhythm of vasopressin and oxytocin in rat retina, pineal and Harderian gland. Peptides 9:289–293PubMedCrossRefGoogle Scholar
- Guerrero JM, Puig-Domingo M, Vaughan GM, Reiter RJ (1987) Characterization of type II thyroxine 5′-deiodinase activity in the rat Harderian gland. Life Sci 41:1179–1185PubMedCrossRefGoogle Scholar
- Guerrero JM, Puig-Domingo M, Santana C, Menendez-Pelaez A, Reiter RJ (1988) Inhibition of pineal type II 5′-deiodinase does not effect the nocturnal increase of N-acetyltransferase activity and melatonin content in either euthyroid or thyroidectomized rats. J Pineal Res 5:513–520PubMedCrossRefGoogle Scholar
- Haldar C, Ghosh M (1989) Effect of pinealectomy and 5-methoxyindoles on Harderian gland activity of the Indian jungle bush quail Perdicula asiatica. Indian J Exp Biol 27:704–708PubMedGoogle Scholar
- Hoffman RA (1971) Influence of some endocrine glands, hormones and blinding on the histology and porphyrins of the Harderian glands of golden hamsters. Am J Anat 132:463–478PubMedCrossRefGoogle Scholar
- Hoffman RA, Reiter RJ (1965a) Pineal gland: influence on gonads of male hamsters. Science 148:1609–1611PubMedCrossRefGoogle Scholar
- Hoffman RA, Reiter RJ (1965b) Rapid pinealectomy in hamsters and other small rodents. Anat Rec 153:19–22PubMedCrossRefGoogle Scholar
- Kappers JA (1960) The development, topographical relations and innervation of the epiphysis cerebri in the albino rat. Z Zellforsch Mikrosk Anat 52:163–215PubMedCrossRefGoogle Scholar
- Klüver H (1944) Porphyrins, the nervous system, and behavior. J Psychol 17:209–217CrossRefGoogle Scholar
- Lopez-Gonzalez MA, Calvo JR, Rubio A, Goberna R, Guerrero JM (1990) Characterization of melatonin-binding sites in the Harderian gland and median eminence of the rat. Life Sci 48:1165–1171CrossRefGoogle Scholar
- Marrufo B, Menendez-Pelaez A, Buzzell GR, Gonzalez-Brito A, Reiter RJ (1989) 5α-Dihydrotestos-terone administration converts indoleamine metabolism and porphyrin content of the female Syrian hamster Harderian gland to the male type. Proc Soc Exp Biol Med 192:192–195PubMedGoogle Scholar
- Menendez-Pelaez A, Reiter RJ, Howes KA, Puig-Domingo M, Vaughan MK, Troiani ME, Little JC (1988a) Harderian gland N-acetyltransferase activity in the male Syrian hamster: effects of gonadectomy, short photoperiod exposure or subcutaneous melatonin implants. Endocr Res 14:121–130PubMedCrossRefGoogle Scholar
- Menendez-Pelaez A, Reiter RJ, Guerrero JM, Santana C, Howes KA, Gonzalez-Brito A (1988b) N-acetyltransferase activity and melatonin concentrations in the Harderian glands of female Syrian hamsters: alterations following either pinealectomy of bilateral superior cervical gan-glionectomy. Biochem Arch 4:231–238Google Scholar
- Menendez-Pelaez A, Buzzell GR, Gonzalez-Brito A, Reiter RJ (1990) Androgenic control of N-acetyltransferase activity in the Harderian glands of the female Syrian hamster is mediated by 5α-dihydrotestosterone. J Cell Biochem 42:95–100PubMedCrossRefGoogle Scholar
- Mhatre MC, van Jaarsveld AS, Reiter RJ, (1988) Melatonin in the lacrimal gland: first demonstration and experimental manipulation. Biochem Biophys Res Commun 153:1186–1192PubMedCrossRefGoogle Scholar
- Noell WK, Walker VS, Kang BS, Berman S (1966) Retinal damage by light in rats. Invest Opthalmol 5:450–473Google Scholar
- Norvell JE, Clabough JW (1972) Adrenergic and cholinergic innervation of the hamster Harderian gland. Science 178:1102–1103PubMedCrossRefGoogle Scholar
- O’Steen WK, Lytle RB (1971) Early cellular disruption and phagocytosis in photically-induced retinal degeneration. Am J Anat 130:227–234PubMedCrossRefGoogle Scholar
- Pang SF, Allen AE (1986) Extra-pineal melatonin in the retina: its regulation and physiological function. Pineal Res Rev 4:55–96Google Scholar
- Pang SF, Brown GM, Grota LJ, Chambers JW, Rodman RL (1977) Determination of N-acetyl-serotonin and melatonin activities in the pineal gland, retina, Harderian gland, brain and serum of rats and chickens. Neuroendocrinology 23:1–13PubMedCrossRefGoogle Scholar
- Panke ES, Reiter RJ, Rollag MD, (1979a) Effect of removal of the Harderian glands on pineal melatonin concentrations in the Syrian hamster, Mesocricetus auratus. Experientia 35:1405–1406PubMedCrossRefGoogle Scholar
- Panke ES, Rollag MD, Reiter RJ (1979b) Pineal melatonin concentrations in the Syrian hamster. Endocrinology 104:194–197PubMedCrossRefGoogle Scholar
- Quay WB (1963) Orcadian rhythm in rat pineal serotonin and its modification by es trous cycle and photoperiod. Gen Comp Endocrinol 3:473–480CrossRefGoogle Scholar
- Reiter RJ (1972) Compensatory growth of the ovaries, adrenal glands and kidneys in blinded, anosmic rats. Experientia 28:1492PubMedCrossRefGoogle Scholar
- Reiter RJ (1973) Comparative effects of continual lighting and pinealectomy on the eyes, the Harderian glands and reproduction in pigmented and albino rats. Comp Biochem Physiol 44A:503–509CrossRefGoogle Scholar
- Reiter RJ (1980) The pineal and its hormones in the control of reproduction in mammals. Endocr Rev 1:109–131PubMedCrossRefGoogle Scholar
- Reiter RJ (1988) Neuroendocrinology of melatonin. In: Miles A, Philbrick DRS, Thompson C (eds) Melatonin: clinical perspectives. Oxford University Press, Oxford, pp 1–42Google Scholar
- Reiter RJ, Hedlund L (1976) Peripheral sympathetic innervation of the deep pineal gland of the golden hamster. Experientia 32:1071–1072PubMedCrossRefGoogle Scholar
- Reiter RJ, Hester RJ (1966) Interrelationships of the pineal gland, the superior cervical ganglia and the photoperiod in the regulation of the endocrine system of hamsters. Endocrinology 79:1168–1170PubMedCrossRefGoogle Scholar
- Reiter RJ, Klein DC (1971) Observations on the pineal gland, the Harderian glands, the retina, and the reproductive organs of adult female rats exposed to continuous light. J Endocrinol 51:117–125PubMedCrossRefGoogle Scholar
- Reiter RJ, Klein DC, Weller JC (1971) Pineal N-acetyltransferase activity in blinded and anosmic rats. Endocrinology 89:1020–1023PubMedCrossRefGoogle Scholar
- Reiter RJ, Richardson BA, Hurlbut EC (1981) Pineal, retinal and Harderian gland melatonin in a diurnal species, the Richardson’s ground squirrel (Spermophilus richardsonii). Neurosci Lett 22:285–288CrossRefGoogle Scholar
- Reiter RJ, Richardson BA, Matthews SA, Lane SJ, Ferguson BN (1983) Rhythms in immunoreactive melatonin in the retina and Harderian gland of rats: persistence after pinealectomy. Life Sci 32:1129–1136CrossRefGoogle Scholar
- Sashima M, Hatakeyama S, Satoh M, Suzuki A (1989) Harderianization is another sexual dimorphism of rat exorbital lacrimal gland. Acta Anat 135:303–306PubMedCrossRefGoogle Scholar
- Sheridan MN, Reiter RJ (1970) Observations on the pineal system in the hamster. II. Fine structure of the deep pineal. J Morphol 131:163–178PubMedCrossRefGoogle Scholar
- Snyder SH, Zweig M, Axelrod J (1964) Control of the circadian rhythm in serotonin content of the rat pineal gland. Life Sci 3:1175–1179PubMedCrossRefGoogle Scholar
- Synder SH, Zweig M, Axelrod J, Fischer JE (1965) Control of the circadian rhythm in serotonin content of the rat pineal gland. Proc Nat Acad Sci 53:301–305CrossRefGoogle Scholar
- Vakkuri O, Rintamäki H, Leppäluoto J (1985a) Plasma and tissue concentrations of melatonin after midnight light exposure and pinealectomy in the pigeon. J Endocrinol 105:263–268PubMedCrossRefGoogle Scholar
- Vakkuri O, Rintamäki H, Leppäluoto J (1985b) Presence of immunoreactive melatonin in different tissues of the pigeon (Columbia livid). Gen Comp Endocrinol 58:69–75PubMedCrossRefGoogle Scholar
- Vilchis F, Hernandez A, Perez AE, Perez-Palacios G (1987) Hormone regulation of the rodent Harderian gland: binding properties of the androgen receptor in the male golden hamster. J Endocrinol 112:3–8PubMedCrossRefGoogle Scholar
- Wetterberg L (1972) Increase in Harderian gland porphyrin content in castrated male hamsters dependent on light and visual function. Life Sci 11 (II):541–546CrossRefGoogle Scholar
- Wetterberg L, Geller E, Yuwiler A (1970a) Harderian gland: an extraretinal photoreceptor influencing the pineal gland in neonatal rats? Science 167:884–885PubMedCrossRefGoogle Scholar
- Wetterberg L, Yuwiler A, Ulrich R, Geller E, Wallace R (1970b) Harderian gland: influence on pineal hydroxyindole-O-methyltransferase activity in neonatal rats. Science 170:194–196PubMedCrossRefGoogle Scholar
- Wetterberg L, Ulrich R, Yuwiler A (1973) Light, the Harderian gland and the rodent pineal. In: Proc 4th Int Congr Endocrinology, Elsevier, New York, p 268Google Scholar
- Wurtman RJ, Axelrod J, Philips LS (1963) Melatonin synthesis in the pineal gland: control by light. Science 142: 1071–1073PubMedCrossRefGoogle Scholar
- Yu HS, Pang SF, Tang PL (1981) Increase in the level of retinal melatonin and persistence of its diurnal rhythm in rats after pinealectomy. J Endocrinol 91:477–481PubMedCrossRefGoogle Scholar
- Zweig M, Snyder SH, Axelrod J (1966) Evidence for a non-retinal pathway of light to the pineal gland of newborn rats. Proc Nat Acad Sci 56:515–519PubMedCrossRefGoogle Scholar