Systemic Ghrelin Treatment Induces Rapid, Transient, and Asymmetric Changes in the Metabolic Activity of the Mouse Brain

Introduction: Ghrelin regulates a variety of functions by acting in the brain. The targets of ghrelin in the mouse brain have been mainly mapped using immunolabeling against c-Fos, a transcription factor used as a marker of cellular activation, but such analysis has several limitations. Here, we used positron emission tomography in mice to investigate the brain areas responsive to ghrelin. Methods: We analyzed in male mice the brain areas responsive to systemically injected ghrelin using positron emission tomography imaging of 18F-fluoro-2-deoxyglucose (18F-FDG) uptake, an indicator of metabolic rate. Additionally, we studied if systemic administration of fluorescent ghrelin or native ghrelin displays symmetric accessibility or induction of c-Fos, respectively, in the brain of male mice. Results: Ghrelin increased 18F-FDG uptake in few specific areas of the isocortex, striatum, pallidum, thalamus, and midbrain at 0–10-min posttreatment. At the 10–20 and 20–30 min posttreatment, ghrelin induced mixed changes in 18F-FDG uptake in specific areas of the isocortex, striatum, pallidum, thalamus, and midbrain, as well as in areas of the olfactory areas, hippocampal and retrohippocampal regions, hypothalamus, pons, medulla, and even the cerebellum. Ghrelin-induced changes in 18F-FDG uptake were transient and asymmetric. Systemically administrated fluorescent-ghrelin-labeled midline brain areas known to contain fenestrated capillaries and the hypothalamic arcuate nucleus, where a symmetric labeling was observed. Ghrelin treatment also induced a symmetric increased c-Fos labeling in the arcuate nucleus. Discussion/Conclusion: Systemically injected ghrelin transiently and asymmetrically affects the metabolic activity of the brain of male mice in a wide range of areas, in a food intake-independent manner. The neurobiological bases of such asymmetry seem to be independent of the accessibility of ghrelin into the brain.

[1]  F. Wasinski,et al.  Characterization of the metabolic differences between male and female C57BL/6 mice. , 2022, Life sciences.

[2]  M. Perelló,et al.  The controversial role of the vagus nerve in mediating ghrelin's actions: gut feelings and beyond , 2022, IBRO neuroscience reports.

[3]  S. Cantel,et al.  Circulating ghrelin crosses the blood-cerebrospinal fluid barrier via growth hormone secretagogue receptor dependent and independent mechanisms , 2021, Molecular and Cellular Endocrinology.

[4]  S. Luquet,et al.  Ghrelin treatment induces rapid and delayed increments of food intake: a heuristic model to explain ghrelin’s orexigenic effects , 2021, Cellular and Molecular Life Sciences.

[5]  M. Michaelides,et al.  Translational PET applications for brain circuit mapping with transgenic neuromodulation tools , 2021, Pharmacology Biochemistry and Behavior.

[6]  M. Perelló,et al.  THE INTRIGUING LIGAND-DEPENDENT AND LIGAND-INDEPENDENT ACTIONS OF THE GROWTH HORMONE SECRETAGOGUE RECEPTOR ON REWARD-RELATED BEHAVIORS , 2020, Neuroscience & Biobehavioral Reviews.

[7]  M. Hallett,et al.  Functional neuroanatomy of the basal ganglia , 2021, Principles and Practice of Movement Disorders.

[8]  L. Ng,et al.  The Allen Mouse Brain Common Coordinate Framework: A 3D Reference Atlas , 2020, Cell.

[9]  T. Horvath,et al.  Metabolic Lateralization in the Hypothalamus of Male Rats Related to Reproductive and Satiety States , 2020, Reproductive Sciences.

[10]  A. McDonald Functional neuroanatomy of the basolateral amygdala: Neurons, neurotransmitters, and circuits. , 2020, Handbook of behavioral neuroscience.

[11]  S. Cantel,et al.  Development of a novel fluorescent ligand of growth hormone secretagogue receptor based on the N-Terminal Leap2 region , 2019, Molecular and Cellular Endocrinology.

[12]  J. Zigman,et al.  Ghrelin's Relationship to Blood Glucose. , 2019, Endocrinology.

[13]  Deranda B. Lester,et al.  Cerebellar Modulation of Mesolimbic Dopamine Transmission Is Functionally Asymmetrical , 2019, The Cerebellum.

[14]  K. Simonyan Recent advances in understanding the role of the basal ganglia , 2019, F1000Research.

[15]  M. Perelló,et al.  Brain accessibility delineates the central effects of circulating ghrelin , 2019, Journal of neuroendocrinology.

[16]  E. Portiansky,et al.  Ghrelin Recruits Specific Subsets of Dopamine and GABA Neurons of Different Ventral Tegmental Area Sub-nuclei , 2018, Neuroscience.

[17]  L. Luyt,et al.  Evidence Supporting a Role for the Blood-Cerebrospinal Fluid Barrier Transporting Circulating Ghrelin into the Brain , 2018, Molecular Neurobiology.

[18]  W. Banks,et al.  Ghrelin transport across the blood–brain barrier can occur independently of the growth hormone secretagogue receptor , 2018, Molecular metabolism.

[19]  A. Dagher,et al.  Ghrelin enhances food odor conditioning in healthy humans: an fMRI study , 2018, bioRxiv.

[20]  M. Schwandt,et al.  Exogenous ghrelin administration increases alcohol self-administration and modulates brain functional activity in heavy-drinking alcohol-dependent individuals , 2018, Molecular Psychiatry.

[21]  R. Cunha,et al.  Central Ghrelin Resistance Permits the Overconsolidation of Fear Memory , 2017, Biological Psychiatry.

[22]  J. Zigman,et al.  Circulating Ghrelin Acts on GABA Neurons of the Area Postrema and Mediates Gastric Emptying in Male Mice , 2017, Endocrinology.

[23]  M. Dresler,et al.  Ghrelin modulates encoding-related brain function without enhancing memory formation in humans , 2016, NeuroImage.

[24]  D. Wesson,et al.  Illustrated Review of the Ventral Striatum's Olfactory Tubercle. , 2016, Chemical senses.

[25]  Philip Gorwood,et al.  New Insights in Anorexia Nervosa , 2016, Front. Neurosci..

[26]  M. Ungureanu,et al.  Effects of ghrelin in energy balance and body weight homeostasis , 2016, Hormones.

[27]  J. Zigman,et al.  Ghrelin activates hypophysiotropic corticotropin-releasing factor neurons independently of the arcuate nucleus , 2016, Psychoneuroendocrinology.

[28]  C. Chen,et al.  Neuroendocrine Regulation of Growth Hormone Secretion. , 2016, Comprehensive Physiology.

[29]  S. Calugi,et al.  Ghrelin response to hedonic eating in underweight and short-term weight restored patients with anorexia nervosa , 2016, Psychiatry Research.

[30]  S. Brimijoin,et al.  Radiometric assay of ghrelin hydrolase activity and 3H-ghrelin distribution into mouse tissues. , 2015, Biochemical pharmacology.

[31]  D. H. Root,et al.  The ventral pallidum: Subregion-specific functional anatomy and roles in motivated behaviors , 2015, Progress in Neurobiology.

[32]  M. Perelló,et al.  Ghrelin Signalling on Food Reward: A Salient Link Between the Gut and the Mesolimbic System , 2015, Journal of neuroendocrinology.

[33]  M. Perelló,et al.  Brain Circuits Mediating the Orexigenic Action of Peripheral Ghrelin: Narrow Gates for a Vast Kingdom , 2015, Front. Endocrinol..

[34]  Minmin Luo,et al.  Whole-brain mapping of the direct inputs and axonal projections of POMC and AgRP neurons , 2015, Front. Neuroanat..

[35]  J. Kehr,et al.  Asymmetry of the endogenous opioid system in the human anterior cingulate: a putative molecular basis for lateralization of emotions and pain. , 2015, Cerebral cortex.

[36]  J. Zigman,et al.  Neuroanatomical characterization of a growth hormone secretagogue receptor‐green fluorescent protein reporter mouse , 2014, The Journal of comparative neurology.

[37]  K. Berridge,et al.  Advances in the neurobiological bases for food ‘liking’ versus ‘wanting’ , 2014, Physiology & Behavior.

[38]  M. Perelló,et al.  Divergent Neuronal Circuitries Underlying Acute Orexigenic Effects of Peripheral or Central Ghrelin: Critical Role of Brain Accessibility , 2014, Journal of neuroendocrinology.

[39]  Jimmy D Bell,et al.  Ghrelin mimics fasting to enhance human hedonic, orbitofrontal cortex, and hippocampal responses to food. , 2014, The American journal of clinical nutrition.

[40]  Paul H. E. Tiesinga,et al.  The Scalable Brain Atlas: Instant Web-Based Access to Public Brain Atlases and Related Content , 2013, Neuroinformatics.

[41]  J. Betley,et al.  Parallel, Redundant Circuit Organization for Homeostatic Control of Feeding Behavior , 2013, Cell.

[42]  M. Perelló,et al.  Analysis of brain nuclei accessible to ghrelin present in the cerebrospinal fluid , 2013, Neuroscience.

[43]  Margot J. Taylor,et al.  The centre of the brain: Topographical model of motor, cognitive, affective, and somatosensory functions of the basal ganglia , 2013, Human brain mapping.

[44]  T. Roux,et al.  Rapid sensing of circulating ghrelin by hypothalamic appetite-modifying neurons , 2013, Proceedings of the National Academy of Sciences.

[45]  J. Obeso,et al.  Functional neuroanatomy of the basal ganglia. , 2012, Cold Spring Harbor perspectives in medicine.

[46]  Johannes E. Schindelin,et al.  Fiji: an open-source platform for biological-image analysis , 2012, Nature Methods.

[47]  Johannes E. Schindelin,et al.  TrakEM2 Software for Neural Circuit Reconstruction , 2012, PloS one.

[48]  M. Dietrich,et al.  Fat incites tanycytes to neurogenesis , 2012, Nature Neuroscience.

[49]  J. Zigman,et al.  Ghrelin Indirectly Activates Hypophysiotropic CRF Neurons in Rodents , 2012, PloS one.

[50]  J. Mclaughlin,et al.  Functional neuroimaging demonstrates that ghrelin inhibits the central nervous system response to ingested lipid , 2012, Gut.

[51]  J. Epelbaum,et al.  Physiological roles of preproghrelin-derived peptides in GH secretion and feeding , 2011, Peptides.

[52]  S. Woods,et al.  Ghrelin Enhances Olfactory Sensitivity and Exploratory Sniffing in Rodents and Humans , 2011, The Journal of Neuroscience.

[53]  P. Ciofi The arcuate nucleus as a circumventricular organ in the mouse , 2011, Neuroscience Letters.

[54]  Satoshi Ikemoto,et al.  Brain reward circuitry beyond the mesolimbic dopamine system: A neurobiological theory , 2010, Neuroscience & Biobehavioral Reviews.

[55]  Kazuomi Kario,et al.  The insular cortex and cardiovascular system: a new insight into the brain-heart axis. , 2010, Journal of the American Society of Hypertension : JASH.

[56]  A. Murphy,et al.  Ghrelin O-acyltransferase (GOAT) is essential for growth hormone-mediated survival of calorie-restricted mice , 2010, Proceedings of the National Academy of Sciences.

[57]  A. Ferguson,et al.  Ghrelin: Central Nervous System Sites of Action in Regulation of Energy Balance , 2010, International journal of peptides.

[58]  Chao-shu Tang,et al.  Ghrelin and Cardiovascular Diseases , 2009, Current Cardiology Reviews.

[59]  K. Kangawa,et al.  Ghrelin: from gene to physiological function. , 2010, Results and problems in cell differentiation.

[60]  R. Palmiter,et al.  Loss of GABAergic Signaling by AgRP Neurons to the Parabrachial Nucleus Leads to Starvation , 2009, Cell.

[61]  A. Ferguson,et al.  Gastrointestinal hormone actions in the central regulation of energy metabolism: potential sensory roles for the circumventricular organs , 2009, International Journal of Obesity.

[62]  Vinal D. Patel,et al.  Metabolic Changes in the Rodent Brain after Acute Administration of Salvinorin A , 2009, Molecular Imaging and Biology.

[63]  Alain Dagher,et al.  Ghrelin modulates brain activity in areas that control appetitive behavior. , 2008, Cell metabolism.

[64]  B. Klapp,et al.  Peripheral injection of ghrelin induces Fos expression in the dorsomedial hypothalamic nucleus in rats , 2006, Brain Research.

[65]  C. Cruz,et al.  The growth hormone secretagogue receptor. , 2008, Vitamins and hormones.

[66]  K. Takayama,et al.  Expression of c-Fos protein in the brain after intravenous injection of ghrelin in rats , 2007, Neuroscience Letters.

[67]  R. C. Pierce,et al.  The mesolimbic dopamine system: The final common pathway for the reinforcing effect of drugs of abuse? , 2006, Neuroscience & Biobehavioral Reviews.

[68]  D. Cummings Ghrelin and the short- and long-term regulation of appetite and body weight , 2006, Physiology & Behavior.

[69]  Roy G. Smith,et al.  Ghrelin amplifies dopamine signaling by cross talk involving formation of growth hormone secretagogue receptor/dopamine receptor subtype 1 heterodimers. , 2006, Molecular endocrinology.

[70]  S. Hyman,et al.  Neural mechanisms of addiction: the role of reward-related learning and memory. , 2006, Annual review of neuroscience.

[71]  W. Banks,et al.  Ghrelin controls hippocampal spine synapse density and memory performance , 2006, Nature Neuroscience.

[72]  A. Craig Forebrain emotional asymmetry: a neuroanatomical basis? , 2005, Trends in Cognitive Sciences.

[73]  P. Hellström,et al.  Effect of peripherally administered ghrelin on gastric emptying and acid secretion in the rat , 2005, Regulatory Peptides.

[74]  M. Ueno,et al.  Immunocytochemical evaluation of the blood-brain barrier to endogenous albumin in the olfactory bulb and pons of senescence-accelerated mice (SAM) , 1996, Histochemistry and Cell Biology.

[75]  R. Sullivan,et al.  Hemispheric Asymmetry in Stress Processing in Rat Prefrontal Cortex and the Role of Mesocortical Dopamine , 2004, Stress.

[76]  B. Klapp,et al.  Intraperitoneal injection of ghrelin induces Fos expression in the paraventricular nucleus of the hypothalamus in rats , 2003, Brain Research.

[77]  B. Halász,et al.  Asymmetry of the neuroendocrine system , 2003, Journal of endocrinological investigation.

[78]  F. Casanueva,et al.  Ghrelin main action on the regulation of growth hormone release is exerted at hypothalamic level. , 2003, The Journal of clinical endocrinology and metabolism.

[79]  S. M. Robinson,et al.  Extent and Direction of Ghrelin Transport Across the Blood-Brain Barrier Is Determined by Its Unique Primary Structure , 2002, Journal of Pharmacology and Experimental Therapeutics.

[80]  Y. Taché,et al.  Peripheral ghrelin selectively increases Fos expression in neuropeptide Y – synthesizing neurons in mouse hypothalamic arcuate nucleus , 2002, Neuroscience Letters.

[81]  G E Hoffman,et al.  Anatomical Markers of Activity in Neuroendocrine Systems: Are we all ‘Fos‐ed out’? , 2002, Journal of neuroendocrinology.

[82]  W. Shimizu,et al.  Hemodynamic, renal, and hormonal effects of ghrelin infusion in patients with chronic heart failure. , 2001, The Journal of clinical endocrinology and metabolism.

[83]  K. Hosoda,et al.  Stomach is a major source of circulating ghrelin, and feeding state determines plasma ghrelin-like immunoreactivity levels in humans. , 2001, The Journal of clinical endocrinology and metabolism.

[84]  K. Moriyama,et al.  A low dose of ghrelin stimulates growth hormone (GH) release synergistically with GH-releasing hormone in humans. , 2001, The Journal of clinical endocrinology and metabolism.

[85]  S. Dickson,et al.  Systemic Administration of Ghrelin Induces Fos and Egr‐1 Proteins in the Hypothalamic Arcuate Nucleus of Fasted and Fed Rats , 2000, Journal of neuroendocrinology.

[86]  T. Hökfelt,et al.  The neuropeptide Y/agouti gene-related protein (AGRP) brain circuitry in normal, anorectic, and monosodium glutamate-treated mice. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[87]  George Paxinos,et al.  The Mouse Brain in Stereotaxic Coordinates , 2001 .

[88]  H. Groenewegen,et al.  The specificity of the ‘nonspecific’ midline and intralaminar thalamic nuclei , 1994, Trends in Neurosciences.

[89]  H. Fukuyama,et al.  The persistence of high uptake of serum albumin in the olfactory bulbs of mice throughout their adult lives. , 1991, Archives of gerontology and geriatrics (Print).

[90]  A. Stoll,et al.  Neurochemical asymmetries in the albino rat's cortex, striatum, and nucleus accumbens. , 1984, Life sciences.

[91]  M. Coltheart Hemispheric asymmetry , 1978, Nature.