Corticotropin releasing factor-binding protein (CRF-BP) as a potential new therapeutic target in Alzheimer’s disease and stress disorders

Alzheimer’s disease is the most common cause of dementia and one of the most complex human neurodegenerative diseases. Numerous studies have demonstrated a critical role of the environment in the pathogenesis and pathophysiology of the disease, where daily life stress plays an important role. A lot of epigenetic studies have led to the conclusion that chronic stress and stress-related disorders play an important part in the onset of neurodegenerative disorders, and an enormous amount of research yielded valuable discoveries but has so far not led to the development of effective treatment strategies for Alzheimer’s disease. Corticotropin-releasing factor (CRF) is one of the major hormones and at the same time a neuropeptide acting in stress response. Deregulation of protein levels of CRF is involved in the pathogenesis of Alzheimer’s disease, but little is known about the precise roles of CRF and its binding protein, CRF-BP, in neurodegenerative diseases. In this review, we summarize the key evidence for and against the involvement of stress-associated modulation of the CRF system in the pathogenesis of Alzheimer’s disease and discuss how recent findings could lead to new potential treatment possibilities in Alzheimer’s disease by using CRF-BP as a therapeutic target.


Release of CRF in response to stress
Stress is a life-saving mechanism that has been shaped and refined throughout evolution 1 . Acute stress leads to an increase in attention and to memory consolidation 2,3 . For example, anxiety is a normal reaction to stress and, if not excessive, is crucial for homeostasis. However, chronic or excessive stress leads to a decrease in performance and cognition, and hence limited adaptation to the stressor 4,5 . Individual kinetics and magnitude of stress response determine its outcome in terms of resilience or development of stress-related disorders 6 . This can occur in every stage of life 5,7 . Already before birth, stressful situations can have a major impact on the future life span of the organism as well as in newborn, young adult, and older stages of life 7,8 .
Stress response is a highly orchestrated mechanism whereby the body rapidly activates the autonomic nervous system and the hypothalamic-pituitary-adrenocortical (HPA) axis 9,10 . By activation of the HPA axis and the autonomic nervous system, an enormous number of hormones, neurotransmitters, and neuropeptides are released as adaptive reactions to restore homeostasis 10 . Corticotropin-releasing factor (CRF) and CRF family peptides ( Fig. 1) are major regulators of stress response due to their ability to integrate physiological responses to react against a stressor, and due to their dual roles as hormones and as neuromodulators [10][11][12] .
As a hormone, the 41-amino acid polypeptide CRF is secreted at the onset of stress in the paraventricular nucleus of the hypothalamus 13 . CRF is delivered via the bloodstream to the anterior pituitary, where it binds to its receptors and stimulates adrenocorticotropic hormone (ACTH) release. ACTH release activates synthesis of corticosteroids in the adrenal cortex: glucocorticoids such as cortisol in humans and corticosterone in rodents 13,14 . Glucocorticoids can exert profound modulatory effects on a variety of brain functions from early sensitive developmental stages to late adulthood. Fetal exposure to exogenous glucocorticoids or prenatal stress can lead to permanent alteration of HPA function and stress-related performance 15 . At the adult stage, high levels of glucocorticoids have been associated with reduced cognitive ability, including poor memory and decreased mental flexibility and processing speed 16 . After crossing the blood-brain barrier, glucocorticoids activate two types of receptors, the glucocorticoid receptor (GR) and the mineralocorticoid receptor (MR), which mediate stress response in the brain 6,17 . MRs are active under basal conditions and have high affinity to glucocorticoids. GRs have low affinity to glucocorticoids and are activated in response to high levels of the hormone during stress 18,19 . To summarize, endogenous corticosteroid secretion from the adrenal cortex is mainly under the control of ACTH produced by the pituitary gland. ACTH secretion is controlled mostly by the hypothalamic CRF. The aforementioned phenomena rely on transcriptional regulation and occur within time frames ranging from hours to weeks 20 .

Roles of CRF as a neuromodulator
In contrast to hormones, neurotransmitters and neuromodulators exhibit fast action, allowing neurons to react to stressful situations on the synaptic level, within milliseconds to minutes 20 . CRF acts as the principal hormone in the HPA axis 21 , as discussed above, and triggers a number of secondary stress-related events such as secretion of the corticosteroids in the adrenal cortex. However, in addition to its action to regulate the HPA axis at the level of the pituitary, CRF is also expressed in different parts of the brain, where it can act as a neuromodulator or neurotransmitter in response to autonomic and behavioral responses 22 . Here, CRF synergizes with corticosteroids to fine-tune stress responses in a short time frame 11,23,24 .
CRF binds to two receptors, CRF-R1 and CRF-R2, with a higher affinity for CRF-R1 23 (Fig. 1). Both are seven-span G-coupled receptors, are expressed in different regions in the brain, and share~70% identity with each other [25][26][27][28] . In addition to CRF, these receptors can bind three other ligands ( Fig. 1): urocortin (UCN) I, UCN II (stresscopinrelated peptide), and UCN III (stresscopin). UCN I can bind to both receptors with similar affinity 29 , UCN II shows preferential binding to CRF-R2, and UCN III selectively binds CRF-R2 23 . Binding of CRF and UCN I to CRF-R1 and CRF-R2 is modulated in vivo and in vitro by the CRF-binding protein (CRF-BP) 30 , a 37 kDa glycoprotein that was first detected in human plasma [31][32][33] . CRF-BP is structurally unrelated to CRF receptors 34 . In vertebrates, CRF-BP binds to both CRF (Ki = 0.2 nM) and UCN I (Ki = 2 nM) with sub-nanomolar affinity ( Fig. 1 and Table 1), which is greater than the affinity between CRF and its receptors. The affinity of CRF-BP for the other CRF family members is substantially lower: for UCN II, the IC50 is 4.4 nM and UCN III has no affinity for CRF-BP, only for CRF-R2 30,35 . This suggests that CRF-BP could differentially modulate the activity of several CRF family members.
The discovery of a rodent-specific splice variant α-isoform of CRF-R2 (sCRF-Rα2), which encodes the soluble ligand-binding domain of CRF-R2 36 , suggests an even greater complexity of the CRF family. Similar to CRF-BP, sCRF-Rα2 binds CRF and UCN I but has a distinct distribution in comparison with CRF-BP 36,37 (Fig. 1). Fig. 1 The CRF family and its relation with CRF-BP. The CRF family consists of two different CRF receptors: CRF-R1 (one functional isoform) and CRF-R2 (three functional isoforms: α, β, γ). The ligands, CRF and UCN I, UCN II and UCN III will bind and will induce G-proteincoupled signaling via CRF-Rs. The arrows represent the affinity between ligand and receptor or ligand and binding protein. The different affinities are represented by the pattern and thickness of the arrow lines; dashed lines will represent lower affinity as compared with solid arrow lines. The weight of the solid lines will give even more detail about the affinity between both ligand and receptor. CRF displays a relatively high affinity for CRF-R1 and CRF-R2. CRF has a comparatively lower affinity for CRF-R2 compared with its affinity for CRF-R1. UCN I has an approximately equal affinity for both receptors, and UCN II and UCN III seem to be selective for CRF-R2. The signaling cascade also includes CRF-BP and the recently identified soluble αisoform of CRF-R2 (sCRF-Rα2). CRF-BP binds to CRF and UCN I with high affinity to modulate the biological activities of the ligands. Both CRF-BP and CRF-Rα2 are able to sequester CRF and UCN I, whereas CRF-BP exerts a low affinity for UCN II. Abbreviations; corticotropinreleasing factor (CRF), urocortin (UCN), CRF receptor 1 (CRF-R1), CRF receptor 2 (CRF-R2), CRF-binding protein (CRF-BP), α-soluble isoform of CRF-R2 (sCRF-Rα2) In bold, receptor activation; underlined, ECD1-binding domain; blue letter, CRF-R2 specific; double underlined, CRF-BP sequence; Ki, binding affinity sCRF-Rα2 is highly expressed in the olfactory bulb, cortex, midbrain, and the pituitary, and lower levels are found in the hypothalamus, pons, medulla, and spinal cord, and shows high overlap with the cellular distribution of CRF-R1 36,38 . In the CNS, CRF-BP is highly expressed in the cortex, olfactory bulb, hippocampus, and amygdala, and is known to inhibit CRF actions in the HPA axis 39,40 . In the brain, CRF-BP function depends on the tissue and cellular context 41 . Here, CRF-BP and CRF exhibit limited coexpression at the cellular level 36,38 . CRF-BP is localized at the CRF target sites such as the prefrontal cortex and amygdala, regions important in stress-related conditions including anxiety and addiction 41 . Notably, there is a difference in expression of the CRF-BP between male and female mice. In females, CRF-BP expression is positively regulated by estrogen and gonadotropin-releasing hormone in pituitary cell types. This increased expression positively correlates with several conditions such as anorexia, mood disorders, and anxiety disorders, which are more prevalent in females 42 .
In addition to its functions in stress, CRF exerts timeand dose-dependent direct actions during learning and memory formation. The exposure of neurons to acute CRF in vitro induces adaptation by spine increase and spine maturation, but exposure to high dosages of the peptide results in spine retraction and loss of synapses in the hippocampus 20,43 . Opposite effects were seen in the cerebellum, where an increase of spines and dendritic complexity was observed in response to physiological concentrations of CRF in organotypic slice cultures 44,45 . Clearly, effects of CRF on cellular plasticity and connectivity are highly dependent on the context, i.e., the administered dose, duration of stimulation, and cellular composition. It was further shown that chronic exposure or high levels of CRF lead to the activation of CRF-R1, and subsequently actin cytoskeleton rearrangements and atrophy of the spines and dendrites over longer time periods 46,47 . This decrease in spines and in dendritic complexity, and changes in synaptic function are cellular hallmarks of cognitive impairment 20 , characteristic, among others, for late stages of neurodegenerative disorders such as Alzheimer's disease 48-50 . Stress as an environmental risk factor in Alzheimer's disease Alzheimer's disease (AD) is an age-dependent neurodegenerative disorder that causes progressive cognitive impairment and structural alterations in the brain. The brains of patients with AD are characterized by the deposition of extracellular amyloid plaques consisting of β-amyloid (Aβ) peptides, the product of the proteolytic processing of the amyloid precursor protein (APP), and by abnormal hyperphosphorylation of the Tau protein, which precipitates in the form of neurofibrillary tangles inside the neurons 48,49 . A hallmark of the disease is the progressive neuronal loss in the hippocampus and cortex, brain structures that are extremely important in memory formation [50][51][52] . The most common form of AD is sporadic AD without a familial link, but genetically the disease presents as both familial and sporadic cases 53 . Despite many years of research, whether all forms of AD have a common underlying etiology remains poorly understood. A major effort in the research field has been put into the investigation of genetic factors, although environmental factors could be similarly or even more important in the onset of the disease 54 .
For example, in an AD mouse model, carrying a mutated form of APP, accumulation of Aβ and hyperphosphorylated Tau has been shown to occur as a result of exposure to high stress levels by acute restrained stress, chronic isolation, and social stress paradigms [55][56][57] . A reduction in the number of mature dendritic spines in a triple-transgenic mouse model of AD (3 × Tg-AD: PS1 (M146V), APP (Swe), tau (P301L)) and increased Aβ levels due to the augmentation of amyloid-β protein precursor processing 58 have been observed in response to short-term stress.
Exposure to stress early in life can contribute to the later development of AD [59][60][61][62] . High and chronic stress levels lead to a hyper-activation of the HPA axis, which correlates with the rate of AD progression 63,64 . At the same time, chronic stress and stress-dependent disorders, such as posttraumatic stress, and major depression disorders have been linked to the hyper-activation of HPA axis and are directly correlated to a dysregulation in the CRF system 11,13 and AD 5,14,15 .
Chronic stress-dependent disorders can trigger and/or facilitate AD. This effect is specific to the onset of depression late in adulthood, but not for early-age depression 65,66 . However, stress-dependent disorders such as depression, anxiety disorders, and mood disorders are often concurrent with AD. Patients with early AD display alterations in mood before or concurrently with initial signs of minor cognitive impairment or memory loss 67,68 . Recently, a unique transgenic rat model of AD, TgF344-AD (APP (Swe), (PS1ΔE9)), has been used to investigate emotional components of AD 69 . Young TgF344-AD rats were tested for spatial memory functions in a Morris water maze and for anxiety-like behavior in an elevated plus maze. TgF344-AD rats showed increased anxiety-like behavior without a significant decline in spatial memory. These results indicate that enhanced anxiety-like behavior correlates with an early stage of AD and can be used as an early marker 58 . Furthermore, depression-like symptoms can accelerate the loss of brain tissue shown in magnetic resonance imagingstudies in patients with early stages of AD [70][71][72] . To summarize, stress can lead to AD and accelerate neurodegeneration, but disease progression can in turn cause disruption of stress response circuits, which can exacerbate stress-like symptoms, forming a vicious cycle 66 . On the other hand, AD is caused by a combination of different factors and not only linked to high and/or chronic stress levels.
The link between CRF and AD As discussed above, the effect of chronic or high levels of stress leads to the hyperactivation of the HPA axis. Besides the elevation of glucocorticoids 73 , clinical studies have documented the CRF dysregulation in patients with AD [74][75][76] . Significant reduction of the CRF immunoreactivity (CRF-IR) was observed in postmortem tissue in the cerebrocortical areas and in the cerebrospinal fluid of patients with AD compared with that in control tissue 75,77,78 . Together with the decrease in CRF-IR, increase in the concentration of the CRF receptors (CRF-Rs) in the cortex has been directly linked to AD 74,79 . CRF-expressing neurons in the paraventricular nucleus of the hypothalamus show elevated levels of CRF mRNA in postmortem brain from AD patients compared with age-matched healthy controls 48 ; however, the number of CRFexpressing cells is not altered. Calcium flux measurements and neuronal death assays in culture suggested a neuroprotective role for CRF in response to Aβ toxicity in AD brain, although this hypothesis was never confirmed by in vivo studies 80 . It has been hypothesized that CRF might stimulate non-amyloidogenic APP cleavage, exerting a beneficial effect on Aβ accumulation 81 . In vivo animal studies identified CRF as a factor that enhances cognition and memory. Upon injection in the amygdala and the ventricles of the rat brain, CRF dose-dependently improved retention of the inhibitory avoidance response and improved acquisition of a visual discrimination task 22,82 . In addition, blockage of CRF in the basolateral amygdala in rats and restoring free levels of CRF afterwards showed improved memory 83 . Notably, these are all aspects of memory and cognition that are significantly impacted in AD patients 84 .
In contrast to these findings, multiple studies have demonstrated that exposure to stress, along with elevated levels of CRF, provoked Aβ neuropathology [85][86][87] . For example, in the 3 × Tg-AD mice 88 , enhanced CRF signaling associated with short-term life stress in adults enhanced the progression of Aβ neuropathology 58 . In parallel, infusion of CRF directly into the hippocampus increased the concentration of two major isoforms of Aβ, namely Aβ40 and Aβ42 85,86 , therefore facilitating AD. Park et al. 89 reported a link between this Aβ-enhancing potential of stress-induced CRF and γ-secretase activity as the underlying mechanism. Further, reduced CRF signaling in CRF-R1-deficient mice or treatment with the antagonist NBI-30775 (also known as R121919) both alleviated the stress-induced aggravation in Aβ pathology in a stress-like paradigm in AD mouse models 90,91 . In addition to increasing Aβ concentration, CRF can also enhance Tau pathology 56,92 . Enhancement of Tau phosphorylation at specific epitopes was observed in CRFoverexpressing mice and could be reversed by the specific CRF-R1 antagonist NBI-30775 93 .
To summarize, chronic stress in combination with high CRF levels can cause stress-dependent disorders, increase the risk of AD, and can lead to other diseases 94 . On the other hand, in neurodegenerative diseases, low CRF concentrations are observed 78,95,96 . Chronic stress leads to HPA axis overstimulation, followed by the generation of high CRF and GRs levels in the blood, which can cause detrimental effects to neurons and their connections. These detrimental effects can lower CRF levels in the brain leading to a decrease in its neuromodulatory functions in memory and cognition 6,58,97 .
As of today, AD remains incurable. There is a clear potential to investigate the link between CRF and AD with a focus on developing CRF-centric therapeutic approaches. Targeting CRF signaling, particularly CRF receptors, in stress disorders has been considered as a valid approach for a considerable time 10 .

Signaling and pharmacology of CRF receptors
CRF-Rs belong to the family of G-protein-coupled receptors (GPCRs). These GPCRs mainly activate Gs, which will in turn increase adenylcyclase and stimulate enzymatic activity. Activation of the CRF-Rs, by CRF or by their other ligands, follows a two-step mechanism. First, the C-terminus of CRF binds to the N-terminus of the CRF-Rs. This first interaction causes a conformational change in the CRF-R, which stabilizes the CRF-CRF-Rs interaction, whereupon the interaction with the Nterminus of CRF initiates, and thereby triggers, cellular signaling by activating G-protein signaling [98][99][100][101][102] . Different ligands cause different conformational changes and consequently lead to binding of different G-proteins that will each activate distinct signaling pathways 103 . For example, in primary cells of pregnant myometrium, upon binding of UCN I with CRF-R1, there is an activation of mitogenactivated protein, which stimulates G q for activation of the IP3-protein kinase signaling pathway; however, CRF binding does not activate the same signaling cascade 104 . CRF-R1 peptide agonists, such as astressin (Ki = 0,7), lack the N-terminus of the CRF (Table 1) but bind with high affinity to the extracellular binding domain to prevent binding of a CRF-R agonist. The lack of the N-terminus prevents G-protein interactions and thus inhibits downstream signaling 101,105 . Conversely, ligands such as αhelical CRF fragment 9-41 that lack the C-terminus (Table 1) can bind with low affinity (Ki = 19) and still will be able to activate the receptor 106,107 . Non-peptide antagonists or small molecule agonists, such as NBI-30775, antalarmin, and CRA-0450, bind almost exclusively to the juxtamembrane region, which partially inhibits CRF-R1 ligand binding by blocking the interaction of a ligand with the juxtamembrane domain, but cannot prevent the binding between the ligand and the extracellular domain of the receptor. NBI-30775, antalarmin, and CRA-0450 are allosteric inhibitors; they do not bind to the N-terminus to activate the receptor, but instead bind to the J-domain where they will cause a conformational change, leading to the inactivation of the receptor ( Table 1).
To date, there are no specific non-peptide or smallmolecule antagonists for CRF-R2 10,108 . CRF-R1 antagonists such as NBI-30775, pexacerfont, and CP-316,311 were the first allosteric GPCR inhibitors in clinical trials against depression and anxiety disorders. However, none of these compounds showed efficacy in advanced trials [109][110][111] . More recent pre-clinical discoveries present a more detailed view on the interaction between a ligand and the CRF-Rs. The observation of receptor association and dissociation revealed a significant difference between lead compounds. These differences could explain the disappointing outcome of previous clinical trials. Future trials could be improved by focusing on maximizing the receptor residence time or adjusting the dosage of antagonist to ensure CRF-R1 in the brain will remain occupied over longer periods 112 . In addition, novel technologies, such as positron emission tomography, genetic screening, and local viral CRF overexpression tools open up new opportunities to develop new compounds that will be more effective to influence CRF-R1 downstream signaling 10,113 .

CRF-BP and treatment of AD
A growing body of evidence suggests a prominent role of CRF-BP in the CRF system. CRF-BP regulates CRF bioavailability in the HPA axis and can restore normal levels of CRF. It is therefore tempting to consider targeting CRF-BP as a potential therapeutic route to control CRF levels, which are disrupted in AD, to improve memory and to delay AD progression.
CRF-BP is highly conserved in gene structure throughout the evolution from invertebrates to humans 114 . Studies have indicated its importance in the regulation of CRF activity 39 . CRF-BP expression is increased in the pituitary and the brain, predominantly by stress 115 . This increased expression of the CRF-BP, specifically in the HPA axis, results in lower levels of free, i.e., CRF-BP-unbound, CRF and suppresses CRF-R1 activation and downstream signaling. CRF-BP is expressed in a highly tissue-specific pattern and differs between species. Human CRF-BP is detected in the plasma, placenta, synovial fluid, amniotic fluid, liver, the pituitary, and the brain 116 . In other species, notably in rodents, CRF-BP expression is exclusively restricted to the brain and the pituitary 32,39 . These species-specific expression patterns represent an important limiting factor in behavioral and in vivo studies for evaluating the full physiological functions of the protein in rodent stress models. In the past, three different mouse models with altered CRF-BP expression were created: two transgenic mouse lines that overexpress CRF-BP and one CRF-BP knockout model [117][118][119][120] (Table 2). Phenotypical studies showed increased anxiety in mice with a CRF-BP-null mutation 117,121 . Unfortunately, no study has so far shown changes in memory consolidation or cognition in these transgenic CRF-BP models. In the human brain, a large portion of CRF appears to be complexed with CRF-BP and therefore likely unavailable for activating CRF-Rs and downstream events 122 . The effective concentration of free CRF is not directly related to total CRF abundance. Instead, the effective concentration is a function of both CRF and CRF-BP levels 116 . Several clinical trials that investigated the inhibition of CRF by blocking its receptor CRF-R1 as a potential treatment for CRF-dependent disorders had negative outcomes, as discussed above. The clinical studies either demonstrated multiple side effects, such as in the case of compound R121919, which caused elevated liver enzymes, or reported a complete lack of efficacy, such as in the case of CP-316,311, verucerfont, and pexacerfont 10,123 . Accordingly, such drugs that directly target the binding of CRF-BP to CRF and indirectly inactivate CRF-R1 may represent attractive nextgeneration candidates for the treatment of stressdependent disorders, potentially including AD.
Using the CRF-BP antagonist ligand CRF 6-33 , Behan et al. 124 showed a restoration of normal brain levels of CRF in AD models. The application of CRF 6-33 increased free levels of CRF and demonstrated cognitionenhancement properties in the Morris water maze paradigm of learning and memory in AD mice. This indirect approach to activate CRF-Rs does not require CRF-R agonists and is consequently unlikely to result in no characteristic side effects of CRF-R agonisms, such as disturbance in anxiety and arousal, which are characteristic to CRF-R1 and not CRF-R2 124,125 . In AD, there is no change in CRF-BP, so the total amount of hCRF does provide a readout of free levels of CRF. Therefore, releasing CRF from its binding protein would elevate the levels of available CRF in the aging brain. Consequently, CRF-BP ligands could potentially be sufficient to alleviate some of the symptoms and memory deficits in AD patients. In addition, the critical role of astrocytes in AD and other neurodegenerative diseases such as amyotrophic lateral sclerosis and multiple sclerosis is currently emerging 126,127 . Astrocytes express and release CRF-BP, and display the highest amount of membrane-bound CRF-BP. The astrocyte-associated CRF-BP reservoir

Phenotype
Increased locomotor activity and a non-significant decrease in anxiety Overexpression of CRF-BP in the brain, the pituitary, and peripheral tissue Attenuation of ACTH secretion after lipopolysaccharide treatment 119 Phenotype

Increased body weight
Knockout models CRF-BP-null mutation (CRF-BP KO) Levels of corticosterone and ACTH were unchanged 117,121 Phenotype Reduced body weight (male mice), increased anxiety (sex dependent) Impairment of maternal aggression but no change of inter male aggression Non-genetic modifications Acute stress condition and/or removal from adrenal glands in rats (adrenalectomy) The acute stress condition: increased CRF-BP expression Adrenalectomy condition: decreased CRF-BP expression 138 Induced stress by food deprivation in rats Increased CRF-BP in basolateral amygdala. Decreased CRF-BP expression in the pituitary and elevated plasma corticosterone 139 The effect of acute and chronic restraint stress, specific on basolateral amygdala and dorsal hippocampus in rats Acute stress condition: increased CRF-BP mRNA expression. Chronic stress condition: no change in CRF-BP mRNA levels in basolateral amygdala. CRF-BP mRNA levels in the hippocampus were unaltered 140 The effect of acute restraint stress in basolateral and central amygdala in rats Increased expression in the basolateral amygdala. No change in CFR-BP expression in the central amygdala. No changes in CRF or CRF-Rs mRNA in both regions 141 Social defeat in male rats There may be an increase in free available CRF 142 Phenotype Impairment of social approach behavior. After adding CRF 6-33 into the bed nuclei of the stria terminals, restored social approach might potentially play a causative role in AD and represent a therapeutic target. Astrocytes have attracted attention due to their role in disease 127 and until now their roles as an important source of CRF-BP have not been broadly investigated in stress-related diseases or neurodegenerative disorders.

Conclusions
Stress and AD are strongly linked to each other. Ligands and receptors of the CRF system have been investigated as therapeutic targets in neuropsychiatric disorders in numerous studies and clinical trials. Interpretation of these data is not always straightforward. As discussed above, effects of CRF as neuropeptide are highly variable depending on the location, dose, and exposure time. Further, a clear distinction must be made between functions as hormone and as neuropeptide, particularly with regard to local vs. systemic and primary vs. secondary effects. Here we provide a rationale for targeting CRF-BP as an alternative approach in AD. Admittedly, there is still a shortage of mechanistic data about CRF-BP and its possible function and distribution in the brain. Two studies investigating the potential roles of CRF-BP in AD focused on its inactivating impact/effect on CRF and UCN I interactions with their receptors 124,125 . In an animal model, by targeting the CRF-BP it was possible to achieve restoration of memory and learning the brain functions impaired in AD 125 . These findings could lead to new treatment possibilities in AD by using CRF-BP as a therapeutic target. The aforementioned studies did not investigate any other possible roles of the binding protein, its possible brain region-specific functions, or its cellular and subcellular localization 124,125 . Furthermore, one needs to consider the difference in AD prevalence between male and female subjects, and the fact that females are more susceptible to develop stress-dependent disorders, correlating with and potentially due to the different distribution pattern of CRF-BP in the brain 42,128 . Nevertheless, CRF-BP appears to be an attractive target for symptomatic treatment in AD. Inhibition of CRF-BP has the potential to boost free CRF levels, which are decreased in AD. Unlike CRF-R1 antagonists, targeting CRF-BP is unlikely to interfere with the HPA axis and to cause pertinent side effects. Clearly, more fundamental research is required prior to any progression to the clinic.