Abstract
Cranial irradiation in prepubertal children with leukemia or brain tumors can lead to precocious or in high doses to late puberty. To unravel the underlying mechanisms, we developed a rat model with selective cranial Co60-irradiation technique. Infantile (12–16 d old) or juvenile (21–23 d old) female Sprague-Dawley rats received a single dose of 4, 5, 6, 9 or 2 × 9 Gy (at days 21 and 23). Each group consisted of 7–20 animals. High radiation doses (9 Gy and more) caused retardation of sexual development, whereas low radiation doses (5 or 6 Gy) led to accelerated onset of puberty in 20% of infantile irradiated rats animals as determined by vaginal opening. Interestingly, at peripubertal age (postnatal day 32–34), 5 or 6 Gy infantile irradiated rats had significantly higher serum LH levels stimulated by GnRH and estradiol levels (p < 0.05). 2 × 9 Gy irradiated rats had at the age of 3 mo a marked growth retardation and significantly lower GH levels than the controls (p < 0.05) whereas prolactin, FSH, TSH, T4, and corticosterone levels were comparable with controls. These studies demonstrate that the GnRH-pulse generator is very radiosensitive as precocious activation occurred after low dose irradiation (5 or 6 Gy) of infantile rats without any other endocrine disorder. High radiation doses (9 or 2 × 9 Gy) induced retardation of sexual maturation and later on growth hormone deficiency. Moreover this model of cranial irradiation seems to be suitable to study the molecular mechanisms of radiation induced pubertal changes.
Similar content being viewed by others
Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
Abbreviations
- Co60:
-
(radioactive) cobalt
- Gy:
-
gray
- T4:
-
thyroxine
- GnRH:
-
gonadotropin-releasing hormone
- TRH:
-
thyroid-releasing hormone
- GHRH:
-
growth hormone releasing hormone
References
Collett-Solberg PF, Sernyak H, Satin-Smith M, Katz LL, Sutton L, Molloy P, Moshang T Jr 1997 Endocrine outcome in long-term survivors of low-grade hypothalamic/chiasmatic glioma. Clin Endocrinol 47: 79–85.
Davies HA, Didcock E, Didi M, Ogilvy-Stuart A, Wales JKH, Shalet SM 1994 Disproportionate short stature after cranial irradiation and combination chemotherapy for leukaemia. Arch Dis Child 70: 472–475.
Müller HL, Klinkhammer-Schalke M, Kühl J 1998 Final height and weight of long-term survivors of childhood malignancies. Exp Clin Endocrinol Diabetes 106: 135–139.
Lannering B, Jansson C, Rosberg S, Albertsson-Wikland K 1997 Increased LH and FSH secretion after cranial irradiation in boys. Med Pediatr Oncol 29: 280–287.
Melin AE, Adan L, Leverger G, Souberbielle JC, Schaison G, Brauner R 1998 Growth hormone secretion, puberty and adult height after cranial irradiation with 18 Gy for leukaemia. Eur J Pediatr 157: 703–707.
Mohnike K, Dörffel W, Timme J, Kluba U, Aumann V, Vorwerk P, Mittler U 1997 Final height and puberty in 40 patients after antileukaemic treatment during childhood. Eur J Pediatr 156: 272–276.
Pinkel D, Woo S 1994 Prevention and treatment of meningeal leukemia in children. Blood 84: 355–366.
Schrappe M, Reiter A, Sauter S, Ludwig WD, Wörmann B, Harbott J, Bender-Götze C, Dörffel W, Dopfer R, Frey E, Havers W, Henze G, Kühl J, Richter R, Ritter J, Treuner J, Zintl F, Odenwald E, Welte K, Riehm H 1994 Konzeption und Zwischenergebnis der Therapiestudie ALL-BFM 90 zur Behandlung der akuten lymphoblastischen Leukämie bei Kindern und Jugendlichen: Die Bedeutung des initialen Therapieansprechens im Blut und Knochenmark. Klin Pädiatr 206: 208–209.
Quigley C, Cowell C, Jiminez M, Burger H, Kirk J, Bergin M, Stevens M, Simpson J, Silink M 1989 Normal or early development of puberty despite gonadal damage in children treated for acute lymphoblastic leukemia. N Engl J Med 321: 143–151.
Ogilvy-Stuart AL, Clayton PE, Shalet SM 1994 Cranial irradiation and early puberty. J Clin Endocrinol Metab 78: 1282–1286.
Rappaport R, Brauner R, Czernichow P, Thibaud E, Renier D, Zucker JM, Lemerle J 1982 Effect of hypothalamic and pituitary irradiation on pubertal development in children with cranial tumors. J Clin Endocrinol Metab 54: 1164–1168.
Canfi A, Chayoth R, Weill S, Bedrak E 1990 The reproductive system of male rats exposed to very low doses of ionizing radiation, hormonal profile of animals exposed after sexual maturity. Andrologia 22: 129–136.
Freud A, Canfi A, Sod-Moriah UA, Chayoth R 1990 Neonatal low-dose gamma irradiation-induced impaired fertility in mature rats. Isr J Med Sci 26: 611–615.
Harms PG, Ojeda SR 1974 A rapid and simple method for chronic cannulation of the jugular vein. J Appl Physiol 36: 391–392.
Aubert ML, Pierroz DD, Gruaz NM, d‘Alleves V, Vuagnat BA, Pralong FP, Blum WF, Sizonenko PC 1998 Metabolic control of sexual function and growth: role of neuropeptide Y and leptin. Mol Cell Endocrinol 140: 107–113.
Roth C, Leonhadt S, Theiling K, Lakomek M, Jarry H, Wuttke W 1998 Ontogeny of the GnRH-, glutaminase- and glutamate decarboxylase-gene in the hypothalamus of female rats. Dev Brain Res 110: 105–114.
Colemann CN 1998 Of what use is molecular biology to the practicing radiation oncologist?. Radiother Oncol 46: 117–125.
Hall E 1993 Nine decades of radiobiology: is radiation therapy any better for it?. Cancer 71: 3753–3766.
Schunior A, Zengel AE, Mullenix PJ, Tarbell NJ, Howes A, Tassinari MS 1990 An animal model to study toxicity of central nervous system therapy for childhood acute lymphoblastic leukemia: effects on growth and craniofacial proportion. Cancer Res 50: 6455–6460.
Wildt L, Marshall G, Knobil E 1980 Experimental induction of puberty in the infantile female rhesus monkey. Endocrinology 131: 1559–1561.
Bourgignon JP, Gerard A, Alvarez Gonzalez ML, Franchimont P 1992 Neuroendocrine mechanisms of onset of puberty. J Clin Invest 90: 1736–1744.
Donoso AO, Lopez FJ, Negro-Vilar A 1992 Cross-talk between excitatory and inhibitory amino acids in the regulation of luteinizing hormone-releasing hormone secretion. Endocrinology 131: 1559–1561.
Moguilevsky JA, Carbone S, Szwarcfarb B, Rondina D 1991 Sexual maturation modifies the GABAergic control of gonadotrophin secretion in female rats. Brain Res 563: 12–16.
Mitsushima D, Hei DL, Terasawa E 1994 γ-Aminobutyric acid is an inhibitory neurotransmitter restricting the release of luteinizing hormone-releasing hormone before the onset of puberty. Proc Natl Acad Sci USA 91: 395–399.
Junier MP, Ma YJ, Costa ME, Hoffman G, Hill DF, Ojeda SR 1991 Transforming growth factor alpha contributes to the mechanism by which hypothalamic injury induces precocious puberty. Proc Natl Acad Sci 88: 9743–9747.
Junier MP, Hill DF, Costa ME, Felder S, Ojeda SR 1993 Hypothalamic lesions that induce female precocious puberty activate glial expression of the epidermal growth factor receptor gene: differential regulation of alternatively spliced transcripts. J Neurosci 13: 703–713.
Ma YJ, Hill DF, Junier MP, Costa ME, Felder SE, Ojeda SR 1994 Expression of epidermal growth factor receptor changes in the hypothalamus during the onset of female puberty. Mol Cell Neurosci 5: 246–262.
Rage F, Hill DF, Sena-Esteves M, Breakefield XO, Coffey RJ, Costa ME, McCann SM, Ojeda SR 1997 Targeting transforming growth factor alpha expression to discrete loci of the neuroendocrine brain induces female sexual precocity. Proc Natl Acad Sci USA 94: 2735–2740.
Ayala ME, Monroy J, Morales L, Castro ME, Dominguez R 1998 Effects of a lesion in the dorsal raphe nuclei performed during the juvenile period of the female rat, on puberty. Brain Res Bull 47: 211–218.
Winterer J, Barnes KM, Lichter AS, Deluca AM, Loriaux DL, Cutler GB Jr 1988 Effect of gonadotropin secretion rate on the radiosensitivity of the rat luteinizing hormone-releasing hormone neuron and gonadotroph. Endocrinology 122: 884–890.
Dörr W, Kummermehr J 1990 Accelerated repopulation of mouse tongue epithelium during fractionated or following single doses. Radiother Oncol 17: 249–259.
Schunior A, Mullenix PJ, Zengel AE, Landy H, Howes A, Tarbell NJ 1994 Radiation effects on growth are altered in rats by prednisone and methotrexate. Pediatr Res 35: 416–423.
Author information
Authors and Affiliations
Additional information
This paper is part of the habilitation thesis of C. Roth.
Rights and permissions
About this article
Cite this article
Roth, C., Schmidberger, H., Schaper, O. et al. Cranial Irradiation of Female Rats Causes Dose-Dependent and Age-Dependent Activation or Inhibition of Pubertal Development. Pediatr Res 47, 586–591 (2000). https://doi.org/10.1203/00006450-200005000-00005
Received:
Accepted:
Issue date:
DOI: https://doi.org/10.1203/00006450-200005000-00005
This article is cited by
-
Radiations and female fertility
Reproductive Biology and Endocrinology (2018)
-
Radiation-induced hypopituitarism after cancer therapy: who, how and when to test
Nature Clinical Practice Endocrinology & Metabolism (2009)
-
Hypopituitarism following radiotherapy
Pituitary (2009)
-
Hypopituitarism As a Consequence of Brain Tumours and Radiotherapy
Pituitary (2005)


