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Alcohol Research: Current Reviews, Volume 34, Issue Number 3


Circadian Genes, the Stress Axis, and Alcoholism

Dipak K. Sarkar, Ph.D., D.Phil.

Dipak K. Sarkar, Ph.D., D.Phil., is the director of and a professor in the Endocrinology Program and Department of Animal Sciences, Rutgers, The State University of New Jersey, New Brunswick, New Jersey.

The body’s internal system to control the daily rhythm of the body’s functions (i.e., the circadian system), the body’s stress response, and the body’s neurobiology are highly interconnected. Thus, the rhythm of the circadian system impacts alcohol use patterns; at the same time, alcohol drinking also can alter circadian functions. The sensitivity of the circadian system to alcohol may result from alcohol’s effects on the expression of several of the clock genes that regulate circadian function. The stress response system involves the hypothalamus and pituitary gland in the brain and the adrenal glands, as well as the hormones they secrete, including corticotrophin-releasing hormone, adrenocorticotrophic hormone, and glucocorticoids. It is controlled by brain-signaling molecules, including endogenous opioids such as β-endorphin. Alcohol consumption influences the activity of this system and vice versa. Finally, interactions exist between the circadian system, the hypothalamic–pituitary–adrenal axis, and alcohol consumption. Thus, it seems that certain clock genes may control functions of the stress response system and that these interactions are affected by alcohol.

Key words: Alcohol consumption; alcohol use, abuse and dependence; alcohol and other drug use pattern; genetics; genetic factors; circadian system; clock genes; stress; stress response; biological adaptation to stress; neurobiology; hypothalamic– pituitary– adrenal axis

Alcohol abuse and dependence are estimated to affect 1 in 8 adults in the United States and several hundred million people worldwide (Grant et al. 2004). To define at-risk populations and develop better treatments, it is important to further identify the genetic and environmental factors that contribute to alcohol addiction. Recent evidence suggests that the body’s internal system that helps control the daily rhythm of the body’s activities (i.e., the circadian system), the body’s stress response system, and the body’s neurobiology of alcohol are extensively intertwined. This article explores some of these interactions.

The Circadian System and Alcohol’s Effects on It

The circadian system—or the body’s internal clock—is a naturally present regulatory system that helps the body maintain an approximately 24-hour cycle in biochemical, physiological, or behavioral processes, thereby allowing the organism to anticipate and prepare for regular environmental changes (i.e., the day–night cycle). For example, circadian rhythms maintain not only sleeping and feeding patterns but also physiological processes such as body temperature, brain-wave activity, hormone production, and cell regeneration. The circadian clockwork results from the interaction of specific clock genes, including genes known as Period (Per1, Per2, and Per3), Clock, Bmal1, and Cryptochrome (Cry1 and Cry2), and others.1 The activity of these genes is controlled by two tightly coupled transcriptional and translational feedback loops that sustain a near 24-hour periodicity of cellular activity. Expression of these clock genes, in turn, regulates the expression of other clock-controlled genes (Ko and Takahashi 2006).

1 By convention, gene names in animals are written in uppercase and lowercase and italicized. Gene names in humans are written in all caps and are italicized, whereas the acronyms for the encoded proteins are all caps but not italicized.

In both humans and animal models, complex bidirectional relationships seem to exist between alcohol intake or exposure and circadian clock systems. The impact of the circadian system on alcohol use is shown by the fact that both preference for and consumption of alcohol are modulated by time of day, and studies found that genetic interactions link core circadian clock genes with alcohol drinking (Spanagel et al. 2005a, b). In addition, disruption of the normal circadian rhythm (i.e., circadian desynchronization) seems to increase the use of alcohol, as seen in frequent travelers and rotating-shift workers, possibly because it frequently activates the body’s stress response (i.e., increases the allostatic load2) (Rosenwasser et al. 2010; Trinkoff and Storr 1998). At the same time, a strong relationship seems to exist between alcohol drinking and altered circadian functions. For example, alcohol intake can alter the following circadian responses:

  • Circadian rhythms in blood pressure, core body temperature, and hormone release in humans (Danel et al. 2009; Devaney et al. 2003; Nakashita et al. 2009);
  • Shifts in the normal circadian rhythm (i.e., circadian phase shifting) and in the free-running period3 in mice (Prosser et al. 2008; Seggio et al. 2009);
  • Return to a normal circadian rhythm after a disruption (i.e., circadian phase resetting) and nocturnal activity patterns in hamsters (Ruby et al. 2009; Seggio et al. 2007); and
  • Rhythmicity in the activity of certain brain cells (i.e., proopiomelanocortin [POMC]4-producing neurons) in a brain region called the hypothalamus (which is involved in the body’s stress system) in rats (Chen et al. 2004).

2 The term allostatic load refers to the physiological consequences of chronic exposure to fluctuating or heightened hormonal responses resulting from repeated or chronic stress.

3 Free-running period is a period that is not adjusted or entrained to the 24-hour cycle in nature or to any artificial cycle.

4 POMC is a precursor molecule primarily produced in and secreted by the pituitary gland but also in the hypothalamus. POMC subsequently can be processed in other tissues into numerous different products, which in turn exert specific effects on the organism and play a role in a wide range of physiological processes. One of these products is adrenocorticotropic hormone (ACTH), which is produced in the pituitary gland and is part of the body’s stress response system, the hypothalamic–pituitary– adrenal (HPA) axis.

Even alcohol exposure before birth can interfere with circadian systems. Thus, prenatal ethanol exposure in rats can alter core body temperature and phase-shifting ability (Sakata- Haga et al. 2006); rhythmic activity of the pituitary gland and the adrenal gland, both of which are part of the body’s stress response system (Taylor et al. 1982); the rhythmic release of the main stress hormone (i.e., corticosterone) (Handa et al. 2006); immune cell rhythms (Arjona et al. 2006); and circadian expression of POMC in the hypothalamus (Chen et al. 2006).

Why Is the Body’s Circadian System So Vulnerable to Alcohol Toxicity?

One logical explanation for the sensitivity of the circadian system to alcohol suggests that alcohol specifically targets one or more of the genes that regulate circadian functions. Using different experimental designs, researchers have demonstrated that alcohol exposure significantly alters the expression of several core clock genes. For example, in chronic alcohol-drinking rats, circadian expression of Per1 and Per2 is significantly disrupted in the hypothalamus (Chen et al. 2006). Likewise, prenatal alcohol exposure alters circadian expression of Per1 and Per2 genes in the hypothalamus and in tissues in other parts of the body in rats and mice (Arjona et al. 2006; Chen et al. 2004; Ko and Takahashi 2006). In addition, neonatal alcohol exposure reduces Cry1 expression in a brain region called the suprachiasmatic nucleus and advances the phase of the Per2 rhythm in the cerebellum and liver (Farnell et al. 2008). In human studies, the expression of clock genes (Per, Cry, and Bmal1) is reduced in white blood cells of male alcoholic patients (i.e., after chronic alcohol exposure) (Huang et al. 2010), whereas alcohol drinking in healthy males (i.e., acute exposure) increases Bmal1 expression in these cells (Ando et al. 2010). Finally, variations of the Per2 gene in which individual DNA building blocks are altered (i.e., single nucleotide polymorphisms [SNPs]) are associated with increased alcohol consumptions in male patients (Spanagel 2005a) and adolescent boys (Comasco et al. 2010). These observations suggest that clock genes are targets through which alcohol may alter circadian functions. However, in-depth molecular studies are necessary to elucidate the potential mechanisms by which alcohol directly or indirectly affects clock gene expression and cellular functions.

Circadian Systems, the Stress Response, and Alcohol Consumption

The Stress Response System

The circadian system also may be involved in regulating alcohol-drinking behavior by interacting with a hormone system called the hypothalamic–pituitary–adrenal (HPA) axis, which plays a central role in the body’s stress response as well as in reward mechanisms. Stress increases the production of a hormone called corticotrophin-releasing hormone (CRH) in certain cells in a region known as the paraventricular nucleus (PVN) in the hypothalamus. The CRH then is secreted into the blood vessels leading to the pituitary gland, where it interacts with a specific molecule, the CRH receptor1 (CRHR1), on specific cells in the anterior pituitary. In response, these cells begin the synthesis and release of adrenocorticotropic hormone (ACTH) into the circulation. ACTH, in turn, stimulates the release of glucocorticoids (i.e., corticosterone in rats and cortisol in humans) from the outer layer (i.e., cortex) of the adrenal glands that are located on top of the kidneys. The glucocorticoids then act on numerous tissues throughout the organism to coordinate the body’s stress response. However, the CRH/CRHR1 system is found not only in the hypothalamus but also in other areas of the brain and helps mediate the actions of the brain’s central stress response systems.

The CRH–HPA system is controlled by many brain-signaling molecules (i.e., neurotransmitters) and their receptors, including opioid peptides5 (e.g., β-endorphin [β-EP]) and their receptors. For example, in rats, the bodies of CRF-producing cells are found in the same locations of the PNV as the fibers of β-EP–releasing cells. In another area of the hypothalamus called the median eminence, a certain type of opioid receptors (i.e., µ-opioid receptors [MOP-r]) is located on the ends of CRH-releasing cells. Agents that stimulate the activity of this receptor (i.e., MOP-r agonists) can inhibit neurotransmitter-stimulated CRF release from the hypothalamus in vitro. Likewise, studies in living organisms found that β-EP infusion decreased CRH release in the blood vessels linking the hypothalamus and the pituitary (Plotsky 1991), and morphine pretreatment prevented stress-induced HPA activation (Zhou et al. 1999). Finally, transplantation of β-EP–producing cells into the PVN suppressed HPA activation under different conditions and normalized stress hyperresponse in fetal alcohol-exposed rats (Boyadjieva et al. 2009). All of these data suggest that endogenous opioids (and, by extension, opiate drugs) have a counterregulatory effect on the stress response.

5 Opioid peptides are short sequences of amino acids (i.e., peptides) that are naturally produced by the body and have effects resembling those of opiate drugs. The three main classes of endogenous opioids are endorphins, enkephalins, and dynorphins. Endorphins also are derived from POMC, which also is the precursor for ACTH.

Alcohol and the Stress Response

In the central nervous system, β-EP long has been suspected of contributing to the positive reinforcement and motivational properties of several addictive substances. For example, microinjection of this peptide to several regions of the brain’s reward system that involves the neurotransmitter dopamine (i.e., the mesolimbic dopamine system), such as the nucleus accumbens, produced place preference (Bals-Kubik et al. 1993). In addition, several studies have demonstrated that repeated administration of alcohol, cocaine, or heroin significantly attenuated β-EP expression in various limbic areas (Jarjour et al. 2009; Rasmussen et al. 2002; Sweep et al. 1988), supporting the notion that β-EP may contribute significantly in the development of alcohol abuse and dependence.

The stress response system also interacts with these reward pathways. For example, the CRH/CRHR1 system can activate mesolimbic dopaminergic pathways and increase dopamine-mediated signal transmission in various parts of the mesolimbic system, including the nucleus accumbens, amygdala, and medial prefrontal cortex. Furthermore, elevation of plasma corticosterone has been associated with increases in alcohol self-administration (Fahlke et al. 1995). Finally, evidence indicates that corticosterone directly stimulates activity of the mesolimbic dopamine system, subsequently increasing drug-seeking behavior (Piazza et al. 1996). Thus, stress, via activation of the CRH–HPA circuits and/or extrahypothalamic CRH circuits, increases mesolimbic dopamine that, in turn, increases drug seeking in drug-treated animals. The relationship between the stress response and the mesolimbic dopamine system is further supported by findings that an abnormality in POMC-mediated regulation of the HPA axis may lead to excess alcohol drinking under stressful conditions. Finally, consistent with animal studies demonstrating acute and chronic effects of alcohol on the HPA axis (Koob and Bloos 1998), studies in humans have documented HPA axis alterations in both actively drinking and recently abstinent alcoholics (Sinha 2007; Uhart and Wand 2009).

Circadian Genes, the Stress Response, and Alcohol

Several findings have suggested that interactions exist between the circadian system, the HPA axis, and alcohol-drinking behavior (see the figure). For example, in animal studies, forced-swimming and immobilization stress elevated expression of the murine Per1 gene in CRH-positive cells of the PVN (Takahashi et al. 2001). On the other hand, stress-related (i.e., cortisol-induced) transcriptional activation of human Per1 was reduced in a type of human blood cells (i.e., B-lymphoblastoid cells) that carried an altered form of the Per1 gene (i.e., the rs3027172 genotype), which has been associated with an increased risk of alcoholism (Dong et al. 2011). Moreover, alcohol consumption can decrease Per2 expression in POMC-producing neurons in the hypothalamus (Chen et al. 2004), and certain mutations in the murine Per2 gene interfere with alcohol’s stimulatory effect on POMC neurons (Agapito et al. 2010) and alter the rhythmic changes in corticosterone levels in the blood (Yang et al. 2009). Thus, it seems that the Per1 and Per2 genes may control functions of CRH- and POMC-producing neurons and that these interactions are affected by alcohol.

Activation of microglia and astrocytes by alcohol in the brain.

Figure Conceptual framework of how the circadian genes regulating stress-induced excess alcohol drinking. Clock genes (Per = P, Cry = C, Bmal1 = B, and Clock = Cl) are key components of the circadian mechanism controlling the functions of nerve cells in the hypothalamus and pituitary that produce two molecules important in the body’s stress response—corticotrophin-releasing hormone (CRH) and proopiomelanocortin (POMC). Of these clock genes, Per might be a potential target of alcohol (indicated by a * symbol) in CRH and POMC neurons and may control the stress-induced propensity to consume alcohol.

NOTE: (+) = stimulatory effect; (–) = inhibitory effect.

It is possible that alcohol-mediated modulation of Per genes may play a significant role in modulating HPA axis function, which in turn may lead to an increased propensity to drink alcohol following a stressful event. This view is supported by the recent findings by Dong and colleagues (2011) that the presence of certain Per1 mutations increased psychosocial stress-induced alcohol drinking in mice, increased alcohol-drinking behavior in human adolescents following psychosocial adversity, and reduced cortisol-induced transcriptional activation of Per1 in human B-lymphoblastoid cells. Other recent findings, although preliminary, showed that a certain Per2 mutation increased basal levels of plasma corticosterone and alcohol drinking while preventing stress-induced increases in corticosterone levels and alcohol drinking in mice (Logan et al. 2011). In this context, it is interesting to note that mice carrying mutations in Per2, but not Per1, display ethanol reinforcement and alcohol-seeking behavior (Spanagel et al. 2005a; Zghoul et al. 2007).


The studies reviewed here suggest an intricate interaction between circadian genes, the body’s stress response, and alcohol consumption. Thus, it seems that particularly the Per1 and Per2 genes, which have a distinct influence on the HPA axis, may control stress-induced propensity to alcohol drinking behavior. However, additional research is needed to address this novel concept involving clock genes, stress, and alcohol drinking.

Financial Disclosure

The author declares that he has no competing financial interests.


Agapito, M.; Mian, N.; Boyadjieva, N.I.; and Sarkar, D.K. Period 2 gene deletion abolishes ß-endorphin neuronal response to ethanol. Alcoholism: Clinical and Experimental Research 34(9):1613–1618, 2010. PMID: 20586752

Ando, H.; Ushijima, K.; Kumazaki, M.; et al. Associations of metabolic parameters and ethanol consumption with messenger RNA expression of clock genes in healthy men. Chronobiology International 27(1):194–203, 2010. PMID: 20205566

Arjona, A.; Boyadjieva, N.; Kuhn, P.; and Sarkar, D.K. Fetal ethanol exposure disrupts the daily rhythms of splenic granzyme B, IFN-gamma, and NK cell cytotoxicity in adulthood. Alcoholism: Clinical and Experimental Research 30(6):1039–1044, 2006. PMID: 16737463

Bals-Kubik, R.; Ableitner, A.; Herz, A.; and Shippenberg, T.S. Neuroanatomical sites mediating the motivational effects of opioids as mapped by the conditioned place preference paradigm in rats. Journal of Pharmacology and Experimental Therapeutics 264(1): 489–495, 1993. PMID: 8093731

Boyadjieva, N.I.; Ortigüela, M.; Arjona, A.; et al. ß-endorphin neuronal cell transplant reduces corticotropin releasing hormone hyperresponse to lipopolysaccharide and eliminates natural killer cell functional deficiencies in fetal alcohol exposed rats. Alcoholism: Clinical and Experimental Research 33(5):931–937, 2009. PMID: 19320628

Chen, C.P.; Kuhn, P.; Advis, J.P.; and Sarkar, D.K. Chronic ethanol consumption impairs the circadian rhythm of pro-opiomelanocortin and period genes mRNA expression in the hypothalamus of the male rat. Journal of Neurochemistry 88(6):1547–1554, 2004. PMID: 15009656

Chen, C.P.; Kuhn, P.; Advis, J.P.; and Sarkar, D.K. Prenatal ethanol exposure alters the expression of period genes governing the circadian function of beta-endorphin neurons in the hypothalamus. Journal of Neurochemistry 97(4):1026–1033, 2006. PMID: 16686691

Comasco, E.; Nordquist, N.; Göktürk, C.; et al. The clock gene PER2 and sleep problems: Association with alcohol consumption among Swedish adolescents. Upsala Journal of Medical Sciences 115(1):41–48, 2010. PMID: 20187847

Danel, T.; Cottencin, O.; Tisserand, L.; and Touitou, Y. Inversion of melatonin circadian rhythm in chronic alcoholic patients during withdrawal: Preliminary study on seven patients. Alcohol and Alcoholism 44(1):42–45, 2009. PMID: 19029096

Devaney, M.; Graham, D.; and Greeley, J. Circadian variation of the acute and delayed response to alcohol: Investigation of core body temperature variations in humans. Pharmacology, Biochemistry, and Behavior 75(4):881–887, 2003. PMID: 12957231

Dong, L.; Bilbao, A.; Laucht, M.; et al. Effects of the circadian rhythm gene period 1 (per1) on psychosocial stress-induced alcohol drinking. American Journal of Psychiatry 168(10):1090–1098, 2011. PMID: 21828288

Fahlke, C.; Hård, E.; Eriksson, C.J.; et al. Consequence of long-term exposure to corticosterone or dexamethasone on ethanol consumption in the adrenalectomized rat, and the effect of type I and type II corticosteroid receptor antagonists. Psychopharmacology (Berl) 117(2):216–224, 1995. PMID: 7753970

Farnell, Y.Z.; Allen, G.C.; Nahm, S.S.; et al. Neonatal alcohol exposure differentially alters clock gene oscillations within the suprachiasmatic nucleus, cerebellum, and liver of adult rats. Alcoholism: Clinical and Experimental Research 32(3):544–552, 2008. PMID: 18215209

Grant, B.F.; Dawson, D.A.; Stinson, F.S. et al. The 12-month prevalence and trends in DSM-IV alcohol abuse and dependence: United States, 1991-1992 and 2001-2002. Drug and Alcohol Dependence 74: 223–234, 2004. PMID: 15194200

Handa, R.J.; Zuloaga, D.G.; and McGivern, R.F. Prenatal ethanol exposure alters core body temperature and corticosterone rhythms in adult male rats. Alcohol 41(8):567–575, 2007. PMID: 18047910

Huang, M.C.; Ho, C.W.; Chen, C.H.; et al. Reduced expression of circadian clock genes in male alcoholic patients. Alcoholism: Clinical and Experimental Research 34(11):1899–1904, 2010. PMID: 20735373

Jarjour, S.; Bai, L.; and Gianoulakis, C. Effect of acute ethanol administration on the release of opioid peptides from the midbrain including the ventral tegmental area. Alcoholism: Clinical and Experimental Research 33(6): 1033–1043, 2009. PMID: 19302084

Ko, C.H., and Takahashi, J.S. Molecular components of the mammalian circadian clock. Human Molecular Genetics 15 (Spec. No. 2):R271–R277, 2006. PMID: 16987893

Koob, G., and Bloom, F.E. Cellular and molecular mechanisms of drug dependence. Science 242(4879):715–723, 1998. PMID: 2903550

Kovanen, L.; Saarikoski, S.T.; Haukka, J.; et al. Circadian clock gene polymorphisms in alcohol use disorders and alcohol consumption. Alcohol and Alcoholism 45(4):303–311, 2010. PMID: 20554694

Logan, R.W.; O’ Connell, S.; Levitt, D.; et al. The involvement of clock gene Per2 in mediating stress-induced alcohol drinking behavior in fetal-alcohol exposed mice. Alcoholism: Clinical and Experimental Research 35:107, 2011.

Nakashita, M.; Ohkubo, T.; Hara, A.; et al. Influence of alcohol intake on circadian blood pressure variation in Japanese men: The Ohasama study. American Journal of Hypertension 22(11):1171–1176, 2009. PMID: 19713946

Perreau-Lenz, S.; Zghoul, T.; de Fonseca, F.R.; et al. Circadian regulation of central ethanol sensitivity by the mPer2 gene. Addiction Biology 14(3):253–259, 2009. PMID: 19523042

Piazza, P.V.; Barrot, M.; Rougé-Pont, F.; et al. Suppression of glucocorticoid secretion and antipsychotic drugs have similar effects on the mesolimbic dopaminergic transmission. Proceedings of the National Academy of Sciences of the United States of America 93(26):15445–15450, 1996. PMID: 8986831

Plotsky, P.M. Pathways to the secretion of adrenocorticotropin: A view from the portal. Journal of Neuroendocrinology 3(1):1–9, 1991. PMID: 19215439

Prosser, R.A.; Mangrum, C.A.; and Glass, J.D. Acute ethanol modulates glutamatergic and serotonergic phase shifts of the mouse circadian clock in vitro. Neuroscience 152(3):837–848, 2008. PMID: 18313227

Rasmussen, D.D.; Boldt, B.M.; Wilkinson, C.W.; and Mitton, D.R. Chronic daily ethanol and withdrawal: 3. Forebrain pro-opiomelanocortin gene expression and implications for dependence, relapse, and deprivation effect. Alcoholism: Clinical and Experimental Research 26(4):535–546, 2002. PMID: 11981131

Rosenwasser, A.M.; Clark, J.W.; Fixaris, M.C.; et al. Effects of repeated light-dark phase shifts on voluntary ethanol and water intake in male and female Fischer and Lewis rats. Alcohol 44(3):229–237, 2010. PMID: 20488643

Rosenwasser, A.M.; Fecteau, M.E.; Logan, R.W.; et al. Circadian activity rhythms in selectively bred ethanol-preferring and nonpreferring rats. Alcohol 36(2):69–81, 2005. PMID: 16396740

Ruby, C.L.; Brager, A.J.; DePaul, M.A.; et al. Chronic ethanol attenuates circadian photic phase resetting and alters nocturnal activity patterns in the hamster. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology 297(3):R729–R737, 2009. PMID: 19553498

Sakata-Haga, H.; Dominguez, H.D.; Sei, H.; et al. Alterations in circadian rhythm phase shifting ability in rats following ethanol exposure during the third trimester brain growth spurt. Alcoholism: Clinical and Experimental Research 30(5):899–907, 2006. PMID: 16634860

Seggio, J.A.; Fixaris, M.C.; Reed, J.D.; et al. Chronic ethanol intake alters circadian phase shifting and free-running period in mice. Journal of Biological Rhythms 24(4):304–312, 2009. PMID: 19625732

Sinha, R. The role of stress in addiction relapse. Current Psychiatry Reports 9(5):388–395, 2007. PMID: 17915078

Spanagel, R.; Pendyala, G.; Abarca, C.; et al. The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption. Nature Medicine 11(1):35–42, 2005a. PMID: 15608650

Spanagel, R.; Rosenwasser, A.M.; Schumann, G.; and Sarkar, D.K. Alcohol consumption and the body’s biological clock. Alcoholism: Clinical and Experimental Research 29(8): 1550–1557, 2005b. PMID: 16156052

Sweep, C.G.; Van Ree, J.M.; and Wiegant, V.M. Characterization of beta-endorphin-immunoreactivity in limbic brain structures of rats self-administering heroin or cocaine. Neuropeptides 12(4):229–236, 1988. PMID: 2976900

Takahashi, S.; Yokota, S.; Hara, R.; et al. Physical and inflammatory stressors elevate circadian clock gene mPer1 mRNA levels in the paraventricular nucleus of the mouse. Endocrinology 142(11):4910–4917, 2001. PMID: 11606459

Taylor, A.N.; Branch, B.J.; Cooley-Matthews, B.; and Poland, R.E. Effects of maternal ethanol consumption in rats on basal and rhythmic pituitary-adrenal function in neonatal offspring. Psychoneuroendocrinology 7(1):49–58, 1982. PMID: 7201653

Trinkoff, A.M., and Storr, C.L. Work schedule characteristics and substance use in nurses. American Journal of Industrial Medicine 34(3): 266–271, 1988. PMID: 9698996

Uhart, M., and Wand, G.S. Stress, alcohol and drug interaction: An update of human research. Addiction Biology 14(1):43–64, 2009. PMID: 18855803

Yang, S.; Liu, A.; Weidenhammer, A.; et al. The role of mPer2 clock gene in glucocorticoid and feeding rhythms. Endocrinology 150(5):2153–2160, 2009. PMID: 19179447

Zghoul, T.; Abarca, C.; Sanchis-Segura, C.; et al. Ethanol self-administration and reinstatement of ethanol-seeking behavior in Per1(Brdm1) mutant mice. Psychopharmacology (Berl) 190(1):13–19, 2007. PMID: 17051414

Zhou, Y.; Spangler, R.; Maggos, C.E.; et al. Hypothalamic-pituitary-adrenal activity and pro-opiomelanocortin mRNA levels in the hypothalamus and pituitary of the rat are differentially modulated by acute intermittent morphine with or without water restriction stress. Journal of Endocrinology 163(2):261–267, 1999. PMID: 10556776

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