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Alcohol and Puberty: Mechanisms of Delayed Development

William L. Dees, Ph.D.; Jill K. Hiney, Ph.D.; and Vinod K. Srivastava, Ph.D.

William L. Dees, Ph.D., is a professor; Jill K. Hiney, Ph.D., is a research assistant professor; and Vinod K. Srivastava, Ph.D., is a research associate professor, all in the Department of Veterinary Integrative Sciences, College of Veterinary Medicine, Texas A&M University, College Station, Texas.

Volume 38, Issue 2 ⦁ Pages: 277-282

    Abstract

    Adolescence represents a vulnerable period for developing youth. Alcohol use and misuse are especially problematic behaviors during this time. Adolescents are more sensitive to alcohol and less tolerant of its detrimental effects than are adults. Research in humans and animals has revealed that early alcohol consumption can result in delayed pubertal development. Animal studies have shown that alcohol detrimentally affects neuroendocrine systems within the hypothalamic region of the brain that are associated with the normal, timely onset of the pubertal process. To effectively restore development and shorten recovery time associated with the adverse effects of alcohol on puberty, researchers must first understand the molecular and physiological mechanisms by which alcohol interferes with critical hypothalamic functions.

    Despite efforts to prevent underage alcohol use, drinking does occur as early as the 6th grade. According to a recent national survey, 9.7 percent of 8th graders and 21.5 percent of 10th graders reported using alcohol at least once in the previous 30 days (Johnston et al. 2016). This is important because people who begin drinking between ages 11 and 14 are at increased risk for developing alcohol use disorder (DeWit et al. 2000), compared with those who begin drinking at later ages. These high-risk age groups also are exactly within the pubertal time frame. Some of the younger adolescents may not have begun the pubertal process. Others, however, are subject to the process being slowed or halted by alcohol, thus impeding further development. Following a brief summary of alcohol’s effects on puberty in humans, this review describes the neuroendocrine processes that control puberty and research using animal models to assess the effects of prepubertal alcohol exposure.

    Early research demonstrated that alcohol use by adolescent boys causes suppressed serum levels of growth hormone (GH), luteinizing hormone (LH), and testosterone (Diamond et al. 1986; Frias et al. 2000a,b), as well as lower bone density (Fehily et al. 1992; Neville et al. 2002). In adolescent girls, alcohol use caused suppressed serum GH and estradiol (E2) levels (Block et al. 1993; Frias et al. 2000b). Other studies found evidence for disruptions in stature, weight distribution, and a risk for nutritional deficiencies (Block et al. 1991; Yamamoto et al. 1991). More recently, studies in girls have shown that prepubertal alcohol use was associated with delayed breast development (Peck et al. 2011) and onset of menarche (Richards et al. 2011). This research suggested that prepubertal girls who use alcohol have four times the chance of delayed onset of puberty than those who do not (Peck et al. 2011). This finding is confirmed in animal models, which show that alcohol acts within the hypothalamic region of the brain to suppress key puberty-related genes and hormones responsible for the normal timing of development.

    Basic Neuroendocrine Control of Puberty

    The onset of puberty results from a complex series of interactions between nerve cells (i.e., neurons) and glial cells (i.e., nonneuronal brain cells) within the hypothalamus that are governed by metabolic signals, as well as genetic and environmental influences. Although age at puberty varies widely between and among mammalian species, the main event that signals puberty onset is basically similar, in that it relies on the increased pulsatile secretory activity of a hypothalamic neuropeptide, luteinizing hormone–releasing hormone (LHRH). This event occurs through the enhanced developmental responsiveness of the LHRH-producing neurons and their nerve terminals to excitatory inputs, such as insulin-like growth factor-1 (IGF-1) (Hiney et al. 1996; Wilson 1998) and the kisspeptins (Kp), a family of neuropeptide products of the KiSS-1 gene (Navarro et al. 2004; Shahab et al. 2005), as well as leptin (Dearth et al. 2000; Lebrethon et al. 2000), transforming growth factor α (Ojeda et al. 1990), and excitatory amino acids (Claypool et al. 2000; Gay and Plant 1987; Urbanski and Ojeda 1990).

    In addition to the development of excitatory inputs, the timing of puberty is influenced by a concomitant and gradual removal of prepubertal inhibitory inputs, such as γ aminobutyric acid (GABA) and the opioid peptides β endorphin and dynorphin (Lehman et al. 2010; Navarro et al. 2009; Srivastava et al. 2015; Terasawa and Fernandez 2001). This alteration, often referred to as a “brake” on the pubertal process, is responsible for keeping prepubertal LHRH secretion low. As LHRH secretion increases, it drives the timing of puberty in both sexes by stimulating pituitary gonadotropin secretions, which in turn stimulate gonadal steroid synthesis and secretions for further maturation of the hypothalamus and reproductive organs. Although all of the excitatory and inhibitory influences noted above have been shown to be involved in the pubertal process, the mechanism-of-action portion of this review will concentrate on the most current findings about some of these modulators in relation to their upstream and downstream influences on the pubertal process.

    Overall Effects of Alcohol on Puberty-Related Hormones and Indices of Pubertal Development

    Initial studies using both female and male rodents revealed that chronic alcohol administration caused delayed puberty (Anderson et al. 1987; Bo et al. 1982; Ramaley 1982). Over the years, researchers have attempted to correlate the timing of puberty with specific puberty-related hormones following chronic prepubertal alcohol exposure. In female rats, alcohol caused delayed vaginal opening and the age at first estrus (Dees and Skelley 1990; Emanuele et al. 2002), as well as suppressed serum levels of GH and LH but not follicle-stimulating hormone (FSH) (Dees and Skelley 1990). In this regard, the differential effects of alcohol on LH and FSH were not surprising, because this previously had been shown in adult rats (Dees and Kozlowski 1984). Significantly, several studies have shown that prepubertal alcohol exposure in females caused suppressed circulating levels of E2 (Bo et al. 1982; Dees and Skelley 1990; Emanuele et al. 2002), a clear indication of impaired ovarian development and activity. Although less is known about the prepubertal effects of alcohol in males, it has been shown to cause an early suppression in serum LH (Cicero et al. 1990) and to reduce the serum levels of GH and testosterone. Prepubertal alcohol use also can lead to lower testicular weight and smaller secondary sex organs (Anderson et al. 1987; Cicero et al. 1990; Emanuele et al. 1999; Tentler et al. 1997).

    Additional research conducted in an animal model that more closely resembled humans, female rhesus monkeys, found that chronically administered alcohol resulted in suppressed GH, LH, and E2 (Dees et al. 2000), exactly as described above in immature female rats. Furthermore, these actions were associated with the altered development of a regular monthly pattern of menstruation (Dees et al. 2000).

    In addition to the effects of alcohol on GH and LH, research has shown that prepubertal alcohol administration caused suppressed serum IGF-1 in immature female rats (Emanuele et al. 2002; Srivastava et al. 1995) and rhesus monkeys (Dees et al. 2000), thereby reducing the amount of peptide available to the prepubertal hypothalamus. This is relevant because IGF-1 normally can act centrally to influence both the hypothalamic–pituitary–gonadal axis and the hypothalamic–pituitary GH axis at puberty. Specifically, IGF-1 has been shown to act at the hypothalamic level to stimulate LHRH/LH secretion (Hiney et al. 1991, 1996) and advance the time of puberty in female rodents (Danilovich et al. 1999; Hiney et al. 1996). The ability of IGF-1 to regulate GH through its actions on hypothalamic growth hormone–releasing hormone and somatostatin (i.e., somatotropin release–inhibiting factor), the latter being a GH-release inhibitor, have been well documented (for review, see Bercu 1996).

    It is important to note that the central control of these two hypothalamic systems is complex and interrelated, especially regarding the important integrative and bidirectional influences of IGF-1 on their respective neuro-secretions. Although a detailed discussion of these basic interrelationships is beyond the scope of this review, it also is worth noting that alcohol can affect both of these systems at multiple levels. For example, in addition to the aforementioned alcohol-related suppression of LHRH/LH resulting in suppressed serum E2, alcohol also causes altered hypothalamic growth hormone–releasing hormone synthesis and secretion (Dees et al. 1990). This then results in decreased pulsatile GH release (Dees et al. 1988), which in turn downregulates IGF-1 synthesis by liver hepatocytes (Srivastava et al. 2002). The resulting alcohol-induced suppression in circulating IGF-1 (Srivastava et al. 1995) causes suppressed body growth and interferes with the maturation and function of several organ systems. Furthermore, the accompanying reduction in circulating IGF-1 to feedback on the hypothalamus further reduces the secretion of LH and GH (for review, see Dees et al. 2009).

    All of the above hormones are critical for puberty. However, alcohol’s suppression of the pituitary secretion of LH has become a primary focus of research on pubertal onset, because this gonadotropin is regulated by LHRH, the hypothalamic peptide responsible for beginning the pubertal process. Researchers now are examining whether the alcohol-induced effect to suppress LH is a result of a hypothalamic or pituitary site of action.

    The Hypothalamic Site of Alcohol’s Actions

    Studies in female rats, which showed increased hypothalamic LHRH content after chronic prepubertal alcohol administration (Dees et al. 1990), offered the first indirect evidence that alcohol affects this part of the brain.Subsequently, alcohol was shown to block the stimulatory effects of norepinephrine (Hiney and Dees 1991), IGF-1 (Hiney et al. 1998), leptin (Hiney et al. 1999), and N-methyl-dl-aspartic acid (NMA) (Nyberg et al. 1993) on the in vitro release of prepubertal LHRH. Although important, these collective observations did not rule out the possibility that alcohol also may act at the level of the pituitary.

    To definitively assess the site of alcohol action, prepubertal rhesus monkeys that had been chronically exposed to alcohol were subjected to hypothalamic and pituitary response tests (Dissen et al. 2004). The hypothalamic stimulation test showed that the NMA-induced LH secretion observed in the non–alcohol-treated monkeys was blocked in the alcohol-treated monkeys. This is significant, because NMA causes LH release by first stimulating hypothalamic LHRH secretion and does not act at the pituitary level. Three weeks later, these same animals were given LHRH to test pituitary responsiveness. Results indicated that the LH response to the peptide was the same in both non–alcohol-treated and alcohol-treated monkeys, conclusively demonstrating the hypothalamic site of action.

    Mechanisms of Action

    Upstream Effects of Alcohol on LHRH Synthesis

    The majority of LHRH-synthesizing neurons are localized within the brain preoptic area and the region just posterior to it referred to as the anterior hypothalamic area. This latter area also contains the anteroventral periventricular (AVPV) nucleus. Neurons in the AVPV nucleus produce kisspeptins, which regulate prepubertal LHRH synthesis and are critical for the onset of puberty (de Roux et al. 2003; Keen et al. 2008; Navarro et al. 2004; Shahab et al. 2005). Thus, research focused on discerning which factors affect prepubertal KiSS-1 expression. Chronic prepubertal alcohol exposure was shown to cause suppressed KiSS-1 gene expression in the AVPV nucleus of female rats, an action associated with a decrease in the usual level of phosphorylated Akt (Srivastava et al. 2009). Akt is a transduction signal that mediates the actions of IGF-1 (Cardona-Gomez et al. 2002), a peptide known to activate puberty in rats and rhesus monkeys (Hiney et al. 1996; Wilson 1998). Understanding IGF-1’s ability to regulate KiSS-1 was essential to further research. In studies with rats, an injection of IGF-1 directly into the brain’s third ventricle caused the upregulation of prepubertal KiSS-1 gene expression in the AVPV nucleus 6 hours later (Hiney et al. 2009). Subsequently, alcohol was shown to block the IGF-1 induction of KiSS-1 in the AVPV nucleus by inhibiting IGF-1 receptor (IGF-1R)-induced phosphorylation of Akt (Hiney et al. 2010). Figure 1 depicts this alcohol action, which leads to suppressed Kp and, subsequently, suppression of LHRH synthesis.

    Image
    Graphic showing blocking of the IGF-1 induction of KiSS-1 in the AVPV nucleus by inhibiting IGF-1 receptor (IGF-1R)-induced phosphorylation of Akt, which leads to suppressed Kp and, subsequently, suppression of LHRH synthesis.
    Figure 1 Alcohol blocks the ability of insulin-like growth factor-1 (IGF-1) to induce the KiSS-1 gene and therefore suppresses production of kisspeptins (Kp), a family of neuropeptide products of KiSS-1, by inhibiting IGF-1 receptor (IGF-1R)-induced phosphorylation of Akt, a transduction signal that mediates the actions of IGF-1. Suppressed Kp production subsequently results in reduced synthesis of luteinizing hormone–releasing hormone (LHRH).

    SOURCE: Hiney et al. 2010.

    Further investigation will determine whether the suppressed Akt activity occurred directly at the level of Kp-containing neurons or through an interneuron or glial cell that also expresses the IGF-1R. However, the fact that alcohol can interfere with this pathway to LHRH synthesis is important, because once the onset of puberty begins, the synthesis of this peptide must keep pace with its release to drive the pubertal process.

    Downstream Effects of Alcohol on LHRH Release

    Alcohol is known to alter several downstream signals in the hypothalamus that collectively reduce LHRH release at puberty. Although the numerous excitatory substances mentioned above influence LHRH at puberty, the role of KiSS-1 and Kp also are noteworthy. KiSS-1 expression increases in the hypothalamus as puberty approaches (Navarro et al. 2004), and Kp is a potent stimulator of prepubertal LHRH secretion (Keen et al. 2008; Navarro et al. 2004). By suppressing prepubertal KiSS-1/Kp (Srivastava et al. 2009), alcohol contributes to decreased LHRH secretion at a time when increases are needed as puberty approaches. In addition, alcohol has been shown to stimulate the release of GABA and the opioid peptides (Lomniczi et al. 2000), which, as stated above, are known inhibitors of LHRH release. Alcohol also can activate the hypothalamic–pituitary–adrenal axis (Rivier 1996), and the hormones involved in the stimulation of this stress axis can suppress LH secretion (Kinsey-Jones et al. 2009; Li et al. 2015). Furthermore, the newly described gene Lin28b also is associated with the brake on puberty, and its expression has been shown to gradually decrease as puberty approaches (Sangiao-Alvarellos et al. 2013).

    Recent research assessed whether alcohol would alter the normal pubertal rise in Kp and decrease in Lin28b protein. Chronic alcohol exposure reversed these actions within the brain region known as the medial basal hypothalamus (MBH) in prepubertal female rats by suppressing Akt, KiSS-1, and Kp (Srivastava et al. 2009, 2015), while stimulating the synthesis of Lin28b (Srivastava et al. 2015). In addition, research showed that Lin28b induced dynorphin (DYN) synthesis and that alcohol stimulated DYN release (Srivastava et al. 2015). DYN inhibits Kp and LHRH secretion (Lehman et al. 2010; Navarro et al. 2009). Because the MBH contains neurons that coexpress Kp and DYN, these observations are relevant to the control of prepubertal LHRH secretion. Figure 2 illustrates the simultaneous and differential effects of alcohol on the excitatory Kp and inhibitory Lin28b pathways. Although LHRH neurons are not localized within the MBH of the rat, they are in primates, including humans. Therefore, both the release and synthesis of LHRH in the MBH of primates may be affected by alcohol.

     

    Image
    Graphic showing the simultaneous and differential effects of alcohol on the excitatory Kp and inhibitory Lin28b pathways.
    Figure 2 Schematic showing the effects of alcohol (ALC) on critical pathways within the hypothalamus that contribute to the control of luteinizing hormone–releasing hormone (LHRH) secretion. (1) Alcohol inhibits Akt, a transduction signal that mediates the actions of insulin-like growth factor-1 (IGF-1). This results in suppressed synthesis of kisspeptins (Kp), peptides that stimulate LHRH secretion. (2) Alcohol prevents the normal pubertal decline in the expression of Lin28b, a gene associated with the brake on puberty, by stimulating its synthesis. (3) Lin28b then stimulates synthesis of dynorphin (DYN), a peptide that inhibits Kp. (4) Alcohol stimulates the release of inhibitory DYN to suppress Kp. (5) The suppressed Kp ultimately results in decreased LHRH release. Red indicates suppression/inhibition; Blue indicates stimulation. For clarity, other factors contributing to LHRH release are not shown.

    In addition to alcohol’s actions on neuronal inputs controlling prepubertal LHRH secretion discussed above, alcohol may affect neuronal-to-glial and glial-to-glial inputs facilitating LHRH release within the MBH. LHRH secretory activity can be modulated by a specific neuronal-glial gene family that synthesizes signaling proteins involved in bidirectional communications at puberty (Ojeda et al. 2010). Chronic prepubertal alcohol exposure decreases the synthesis of glial protein tyrosine phosphatase-β, which is required for binding to the neuronal components contactin and contactin-associated protein-1. This finding demonstrates that alcohol can alter these interactions and interfere with glial–neuronal communications (Srivastava et al. 2011a).

    Glial-to-glial interactions also are affected by alcohol. Once released, glial-derived epidermal growth factor and transforming growth factor α (TGFα) both bind to the erbB1 receptor on adjacent glial cells and stimulate the release of prostaglandin E2 (PGE2) (Ma et al. 1997), a well-known stimulator of LHRH secretion. Alcohol exposure initially was shown to inhibit PGE2 release induced by epidermal growth factor/TGFα (Hiney et al. 2003). In addition, glial-derived IGF-1 binds to IGF-1R on adjacent glial cells, which produce TGFα, and alcohol exposure altered the synthesis and release of TGFα (Srivastava et al. 2011b) and PGE2 (Hiney et al. 1998; Srivastava et al. 2011b), thereby resulting in decreased prepubertal LHRH secretion. Furthermore, specialized glial cells within the MBH known as tanycytes release glial-derived TGFβ1, causing retraction of their processes and allowing for better entry of LHRH into the system of blood vessels that connect the hypothalamus with the pituitary (i.e., hypophyseal portal system) (Prevot et al. 2003). Alcohol blocks IGF-1 from stimulating the synthesis and release of TGFβ1 by altering the IGF-1R synthesis and Akt phosphorylation, therefore further contributing to diminished LHRH secretion (Hiney et al. 2014).

    Conclusion

    Alcohol use and misuse by adolescents increases the risk for altered neuro-endocrine function, potentially modifying the timing of pubertal development. This review highlights results of research with animal models showing the site and mechanisms by which alcohol causes puberty-related problems. These studies demonstrate that alcohol acts within the hypothalamus to alter the expression and function of excitatory and inhibitory puberty-related genes and neuro-hormones, which are critical for the timely increase in LHRH secretion and the onset of puberty. More research in this field is needed and would no doubt promote a better understanding of normal mechanisms controlling events leading to increased LHRH release at puberty, as well as the cause-and-effect relationships by which alcohol can differentially affect them.

    Advancing knowledge in this area will allow researchers to begin to identify potential treatment substances that may lessen the impact and shorten the recovery time of adolescents who show signs of delayed development associated with alcohol use and misuse. It also is significant that delayed puberty is known to be associated with altered gonadal steroid production, which is needed for the development and function of several body systems. Furthermore, delayed pubertal development correlates with other health concerns such as altered bone density or height and weight issues, as well as psychological problems. Thus, the neuroendocrine consequences of alcohol use can result in far-reaching adolescent health concerns.

     

    Acknowledgments

    Supported by National Institutes of Health Grant AA–007216.

    Disclosures

    The authors declare that they have no competing financial interests.

    References

     

    Anderson, R.A., Jr.; Willis, B.R.; Phillips, J.F.; et al. Delayed pubertal development of the male reproductive tract associated with chronic ethanol ingestion. Biochemical Pharmacology 36(13):2157–2167, 1987. PMID: 3606634

    Bercu, B.B. Disorders of growth hormone secretion. In: Lifshitz, F., Ed. Pediatric Endocrinology. 3rd ed. New York: Marcel Dekker, Inc., 1996, pp. 45–59.

    Block, G.D.; Yamamoto, M.E.; and Ishii, E. Association of adolescent alcohol consumption with growth and body composition. Alcoholism: Clinical and Experimental Research 15(1):361, 1991.

    Block, G.D.; Yamamoto, M.E.; Mallick, A.; et al. Effects on pubertal hormones by ethanol abuse in adolescents. Alcoholism: Clinical and Experimental Research 17(2):505, 1993.

    Bo, W.J.; Krueger, W.A.; Rudeen, P.K.; and Symmes, S.K. Ethanol-induced alterations in the morphology and function of the rat ovary. Anatomical Record 202(2):255–260, 1982. PMID: 7199834

    Cardona-Gomez, G.P.; Mendez, P.; and Garcia-Segura, L.M. Synergistic interaction of estradiol and insulin-like growth factor-1 in the activation of PI3K/Akt signaling in the adult rat hypothalamus. Brain Research: Molecular Brain Research 107(1):80–88, 2002. PMID: 12414126

    Cicero, T.J.; Adams, M.L.; O’Connor, L.; et al. Influence of chronic alcohol administration on representative indices of puberty and sexual maturation in male rats and the development of their progeny. Journal of Pharmacology and Experimental Therapeutics 255(2):707–715, 1990. PMID: 2243349

    Claypool, L.E.; Ksuya, E.; Saitoh, Y.; et al. N-methyl D,L-aspartate induces the release of luteinizing hormone-releasing hormone in the prepubertal and pubertal rhesus monkey as measured by in vivo push-pull perfusion in the stalk-median eminence. Endocrinology 141(1):219–228, 2000. PMID: 10614642

    Danilovich, N.; Wernsing, D.; Coschigano, K.T.; et al. Deficits in female reproductive function in GH-R-KO mice: Role of IGF-1. Endocrinology 140(6):2637–2640, 1999. PMID: 10342852

    Dearth, R.K.; Hiney, J.K.; and Dees, W.L. Leptin acts centrally to induce the prepubertal secretion of luteinizing hormone in the female rat. Peptides 21(3):387–392, 2000. PMID: 10793221

    Dees, W.L., and Kozlowski, G.P. Differential effects of ethanol on luteinizing hormone, follicle stimulating hormone and prolactin secretion in the female rat. Alcohol 1(6):429–433, 1984. PMID: 6443069

    Dees, W.L., and Skelley, C.W. Effects of ethanol during the onset of female puberty. Neuroendocrinology 51(1):64–69, 1990. PMID: 2106089

    Dees, W.L.; Dissen, G.A.; Hiney, J.K.; et al. Alcohol ingestion inhibits the increased secretion of puberty-related hormones in the developing female rhesus monkey. Endocrinology 141(4):1325–1331, 2000. PMID: 10746635

    Dees, W.L.; Skelley, C.W.; Hiney, J.K.; and Johnston, C.A. Actions of ethanol on hypothalamic and pituitary hormones in prepubertal female rats. Alcohol 7(1):21–25, 1990. PMID: 1968748

    Dees, W.L.; Skelley, C.W.; Rettori, V.; et al. Influence of ethanol on growth hormone secretion in adult and prepubertal female rats. Neuroendocrinology 48(5):495–499, 1988. PMID: 3244403

    Dees, W.L.; Srivastava, V.K.; and Hiney, J.K. Actions and interactions of alcohol and insulin-like growth factor-1 on female pubertal development. Alcoholism: Clinical and Experimental Research 33(11):1847−1856, 2009. PMID: 19719789

    de Roux, N.; Genin, E.; Carel, J.C.; et al. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proceedings of the National Academy of Sciences of the United States of America 100(19):10972–10976, 2003. PMID: 12944565

    DeWit, D.J.; Adlaf, E.M.; Offord, D.R.; and Ogborne, A.C. Age at first alcohol use: A risk for the development of alcohol disorders. American Journal of Psychiatry 157(5):745–750, 2000. PMID: 10784467

    Diamond, F., Jr.; Ringenberg, L.; MacDonald, D.; et al. Effects of drug and alcohol abuse upon pituitary-testicular function in adolescent males. Journal of Adolescent Health Care 7(1):28–33, 1986. PMID: 2935515

    Dissen, G.A.; Dearth, R.K.; Scott, H.M.; et al. Alcohol alters luteinizing hormone secretion in immature female rhesus monkeys by a hypothalamic action. Endocrinology 145(10):4558–4564, 2004. PMID: 15217984

    Emanuele, M.A.; LaPaglia, N.; Steiner, J.; et al. Effects of nitric oxide synthase blockade on the acute response of the reproductive axis to ethanol in pubertal male rats. Alcoholism: Clinical and Experimental Research 23(5):870–877, 1999. PMID: 10371408

    Emanuele, N.; Ren, J.; LaPaglia, N.; et al. EtOH disrupts female mammalian puberty: Age and opiate dependence. Endocrine 18(3):247–254, 2002. PMID: 12450316

    Fehily, A.M.; Coles, R.J.; Evans, W.D.; and Elwood, P.C. Factors affecting bone density in young adults. American Journal of Clinical Nutrition 56(3):579–586, 1992. PMID: 1503072

    Frias, J.; Rodriguez, R.; Torres, J.M.; et al. Effects of acute alcohol intoxication on pituitary–gonadal axis hormones, pituitary-adrenal axis hormones, beta–endorphin and prolactin in human adolescents of both sexes. Life Sciences 67(9):1081–1086, 2000a. PMID: 10954041

    Frias, J.; Torres, J.M.; Rodriguez, R.; et al. Effects of acute alcohol intoxication on growth axis in human adolescents of both sexes. Life Sciences 67(22):2691–2697, 2000b. PMID: 11105985

    Gay, V.L., and Plant, T.M. N-methyl-D,L-aspartate elicits hypothalamic gonadotropin-releasing hormone release in prepubertal male rhesus monkeys (Macaca mulatta). Endocrinology 120(6):2289–2296, 1987. PMID: 3106017

    Hiney, J.K., and Dees, W.L. Ethanol inhibits luteinizing hormone-releasing hormone release from the median eminence of prepubertal female rats in vitro: Investigation of its actions on norepinephrine and prostaglandin-E2. Endocrinology 128(3):1404–1408, 1991. PMID: 1999162

    Hiney, J.K.; Dearth, R.K.; Lara, F. 3rd; et al. Effects of ethanol on leptin secretion and the leptin-induced luteinizing hormone (LH) from late juvenile female rats. Alcoholism: Clinical and Experimental Research 23(11):1785–1792, 1999. PMID: 10591595

    Hiney, J.K.; Dearth, R.K.; Srivastava, V.K.; et al. Actions of ethanol on epidermal growth factor receptor activated luteinizing hormone secretion. Journal of Studies on Alcohol 64(6):809–816, 2003. PMID: 14743943

    Hiney, J.K.; Ojeda, S.R.; and Dees, W.L. Insulin-like growth factor 1: A possible metabolic signal involved in the regulation of female puberty. Neuroendocrinology 54(4):420–423, 1991. PMID: 1758585

    Hiney, J.K.; Srivastava, V.K.; and Dees, W.L. Insulin-like growth factor-1 stimulation of hypothalamic KiSS-1 gene expression is mediated by Akt: Effect of alcohol. Neuroscience 166(2):625–632, 2010. PMID: 20034543

    Hiney, J.K.; Srivastava, V.; Lara T.; and Dees, W.L. Ethanol blocks the central action of IGF-1 to induce luteinizing hormone secretion in the prepubertal female rat. Life Sciences 62(4):301–308, 1998. PMID: 9450501

    Hiney, J.K.; Srivastava, V.; Nyberg, C.L.; et al. Insulin-like growth factor-1 of peripheral origin acts centrally to accelerate the initiation of female puberty. Endocrinology 137(9):3717–3728, 1996. PMID: 8756538

    Hiney, J.K.; Srivastava, V.K.; Pine, M.D.; and Dees, W.L. Insulin-like growth factor-1 activates KiSS-1 gene expression in the brain of the prepubertal female rat. Endocrinology 150(1):376–384, 2009. PMID: 18703622

    Hiney, J.K.; Srivastava, V.K.; Volz, C.E.; and Dees, W.L. Alcohol alters insulin-like growth factor-1-induced transforming growth factor ß1synthesis in the medial basal hypothalamus of the prepubertal female rat. Alcoholism: Clinical and Experimental Research 38(10):2572–2578, 2014. PMID: 25335926

    Johnston, L.D.; O’Malley, P.M.; Miech, R.A.; et al. Monitoring the Future: National Survey Results on Drug Use, 1975−2015: Overview, Key Findings on Adolescent Drug Use. Ann Arbor: Institute for Social Research, University of Michigan, 2016. Available at: http://monitoringthefuture.org/pubs/monographs/mtf-overview2015.pdf. Accessed May 24, 2016.

    Keen, K.L.; Wegner, F.H.; Bloom, S.R.; et al. An increase in kisspeptin-54 release occurs with the pubertal increase in luteinizing hormone-releasing hormone-1 release in the stalk-median eminence of female rhesus monkeys in vivo. Endocrinology 149(8):4151–4157, 2008. PMID: 18450954

    Kinsey-Jones, J.S.; Li, X.F.; Knox, A.M.; et al. Down-regulation of hypothalamic kisspeptin and its receptor, Kiss1r, mRNA expression is associated with stress-induced suppression of luteinizing hormone secretion in the female rat. Journal of Neuroendocrinology 21(1):20–29, 2009. PMID: 19094090

    Lebrethon, M.C.; Vandersmissen, E.; Gerard, A.; et al. In vitro stimulation of the prepubertal rat gonadotropin-releasing hormone pulse generator by leptin and neuropeptide Y through distinct mechanisms. Endocrinology 141(4):1464–1469, 2000. PMID: 10746651

    Lehman, M.N.; Coolen, L.M.; and Goodman, R.L. Minireview: Kisspeptin/neurokinin B/dynorphin (KNDy) cells of the arcuate nucleus: A central node in the control of gonadotropin-releasing hormone secretion. Endocrinology 151(8):3479–3489, 2010. PMID: 20501670

    Li X.; Shao, B.; Lin, C.; et al. Stress-induced inhibition of LH pulses in female rats: Role of GABA in arcuate nucleus. Journal of Molecular Endocrinology 55(1):9–19, 2015. PMID: 25999179

    Lomniczi, A.; Mastronardi, C.A.; Faletti, A.G.; et al. Inhibitory pathways and the inhibition of luteinizing hormone-releasing hormone release by alcohol. Proceedings of the National Academy of Sciences of the United States of America 97(5):2337–2342, 2000. PMID: 10688896

    Ma, Y.J. ; Berg-von der Emde, K.; Rage, F.; et al. Hypothalamic astrocytes respond to transforming growth factor-alpha with secretion of neuroactive substances that stimulate the release of luteinizing hormone-releasing hormone. Endocrinology 138(1):19–25, 1997. PMID: 8977380

    Navarro, V.M.; Castellano, J.M.; Fernández-Fernández, R.; et al. Developmental and hormonally regulated messenger ribonucleic acid expression of KiSS-1 and its putative receptor, GPR54, in rat hypothalamus and potent luteinizing hormone-releasing activity of KiSS-1 peptide. Endocrinology 145(10):4565–4574, 2004. PMID: 15242985

    Navarro, V.M.; Gottsch, M.L.; Chavkin, C.; et al. Regulation of gonadotropin-releasing hormone secretion by kisspeptin/dynorphin/neurokinin B neurons in the arcuate nucleus of the mouse. Journal of Neuroscience 29(38):11859–11866, 2009. PMID: 19776272

    Neville, C.E.; Murray, L.J.; Boreham, C.A.; et al. Relationship between physical activity and bone mineral status in young adults: The Northern Ireland Young Hearts Project. Bone 30(5):792–798, 2002. PMID: 11996922

    Nyberg, C.L.; Hiney, J.K.; Minks, J.B.; and Dees, W.L. Ethanol alters N-methyl-DL-aspartic acid-induced secretion of luteinizing hormone releasing hormone and the onset of puberty in the female rat. Neuroendocrinology 57(5):863–868, 1993. PMID: 8413822

    Ojeda, S.R.; Dubay, C.; Lomniczi, A.; et al. Gene networks and the neuroendocrine regulation of puberty. Molecular and Cellular Endocrinology 324(1–2):3–11, 2010. PMID: 20005919

    Ojeda, S.R.; Urbanski, H.F.; Costa, M.E.; et al. Involvement of transforming growth factor alpha in the release of luteinizing hormone-releasing hormone from the developing female hypothalamus. Proceedings of the National Academy of Sciences of the United States of America 87(24):9698–9702, 1990. PMID: 2263621

    Peck, J.D.; Peck, B.M.; Skaggs, V.J.; et al. Socio-environmental factors associated with pubertal development in female adolescents: The role of tobacco and alcohol use. Journal of Adolescent Health 48(3):241–246, 2011. PMID: 21338894

    Prevot, V.; Cornea, A.; Mungenast, A.; et al. Activation of erbB-1 signaling in tanycytes of the median eminence stimulates transforming growth factor beta1 release via prostaglandin E2 production and induces cell plasticity. Journal of Neuroscience 23(33):10622–10632, 2003. PMID: 14627647

    Ramaley, J.A. The regulation of gonadotropin secretion in immature ethanol-treated male rats. Journal of Andrology 3(4):248–255, 1982.

    Richards, M.A., and Oinonen, K.A. Age at menarche is associated with divergent alcohol use patterns in early adolescence and early adulthood. Journal of Adolescence 34(5):1065–1076, 2011. PMID: 21115194

    Rivier, C. Alcohol stimulates ACTH secretion in the rat: Mechanisms of action and interactions with other stimuli. Alcoholism: Clinical and Experimental Research 20(2):240–254, 1996. PMID: 8730214

    Sangiao-Alvarellos, S.; Manfredi-Lozano, M.; Ruiz-Pino, F.; et al. Changes in hypothalamic expression of the Lin28/let-7 system and related microRNAs during postnatal maturation and after experimental manipulations of puberty. Endocrinology 154(2):942–955, 2013. PMID: 23291449

    Shahab, M.; Mastronardi, C.; Seminara, S.B.; et al. Increased hypothalamic GPR54 signaling: A potential mechanism for initiation of puberty in primates. Proceedings of the National Academy of Sciences of the United States of America 102(6):2129–2134, 2005. PMID: 15684075

    Srivastava, V.K.; Dearth, R.K.; Hiney, J.K.; et al. Alcohol suppresses insulin-like growth factor-1 gene expression in prepubertal transgenic female mice overexpressing the bovine growth hormone gene. Alcoholism: Clinical and Experimental Research 26(11):1697–1702, 2002. PMID: 12436059

    Srivastava, V.K.; Hiney, J.K.; and Dees, W.L. Short-term alcohol administration alters KiSS-1 gene expression in the reproductive hypothalamus of prepubertal female rats. Alcoholism: Clinical and Experimental Research 33(9):1605–1614, 2009. PMID: 19519717

    Srivastava, V.K.; Hiney, J.K.; and Dees, W.L. Hypothalamic actions and interactions of alcohol and IGF-1 on the expression of glial receptor protein tyrosine phosphatase-β during female pubertal development. Alcoholism: Clinical and Experimental Research 35(10):1812–1821, 2011a. PMID: 21595703

    Srivastava, V.K.; Hiney, J.K.; and Dees, W.L. Prepubertal ethanol exposure alters hypothalamic transforming growth factor-α and erbB1 receptor signaling in the female rat. Alcohol 45(2):173–181, 2011b. PMID: 20926228

    Srivastava, V.; Hiney, J.K.; Nyberg, C.L.; and Dees, W.L. Effect of ethanol on the synthesis of insulin-like growth factor-1 (IGF-1) and the IGF-1 receptor in late prepubertal female rats: A correlation with serum
    IGF-1. Alcoholism: Clinical and Experimental Research 19(6):1467–1473, 1995. PMID: 8749812

    Srivastava, V.K.; Hiney, J.K.; Stevener, K.; and Dees, W.L. Differential effects of alcohol on excitatory and inhibitory puberty-related peptides in the basal hypothalamus of the female rat. Alcoholism: Clinical and Experimental Research 39(12):2386–2393, 2015. PMID: 26608747

    Tentler, J.J.; Lapaglia, N.; Steiner, J.; et al. Ethanol, growth hormone and testosterone in peripubertal rats. Journal of Endocrinology 152(3):477–487, 1997. PMID: 9071969

    Terasawa, E., and Fernandez, D.L. Neurobiological mechanisms of the onset of puberty in primates. Endocrine Reviews 22(1):111–151, 2001. PMID: 11159818

    Urbanski, H.F., and Ojeda, S.R. A role for N-methyl-D-aspartate (NMDA) receptors in the control of LH secretion and initiation of female puberty. Endocrinology 126(3):1774–1776, 1990. PMID: 1968384

    Wilson, M.E. Premature elevation in serum insulin-like growth factor-1 advances first ovulation in rhesus monkeys. Journal of Endocrinology 158(2):247–257, 1998. PMID: 9771469

    Yamamoto, M.E.; Block, G.D., and Ishii, E. Food patterns among adolescents: Influence of alcohol consumption. Alcoholism: Clinical and Experimental Research 15:359, 1991.