Literature DB >> 25978516

Hindbrain Catecholamine Neurons Activate Orexin Neurons During Systemic Glucoprivation in Male Rats.

Ai-Jun Li1, Qing Wang1, Megan M Elsarelli1, R Lane Brown1, Sue Ritter1.   

Abstract

Hindbrain catecholamine neurons are required for elicitation of feeding responses to glucose deficit, but the forebrain circuitry required for these responses is incompletely understood. Here we examined interactions of catecholamine and orexin neurons in eliciting glucoprivic feeding. Orexin neurons, located in the perifornical lateral hypothalamus (PeFLH), are heavily innervated by hindbrain catecholamine neurons, stimulate food intake, and increase arousal and behavioral activation. Orexin neurons may therefore contribute importantly to appetitive responses, such as food seeking, during glucoprivation. Retrograde tracing results showed that nearly all innervation of the PeFLH from the hindbrain originated from catecholamine neurons and some raphe nuclei. Results also suggested that many catecholamine neurons project collaterally to the PeFLH and paraventricular hypothalamic nucleus. Systemic administration of the antiglycolytic agent, 2-deoxy-D-glucose, increased food intake and c-Fos expression in orexin neurons. Both responses were eliminated by a lesion of catecholamine neurons innervating orexin neurons using the retrogradely transported immunotoxin, anti-dopamine-β-hydroxylase saporin, which is specifically internalized by dopamine-β-hydroxylase-expressing catecholamine neurons. Using designer receptors exclusively activated by designer drugs in transgenic rats expressing Cre recombinase under the control of tyrosine hydroxylase promoter, catecholamine neurons in cell groups A1 and C1 of the ventrolateral medulla were activated selectively by peripheral injection of clozapine-N-oxide. Clozapine-N-oxide injection increased food intake and c-Fos expression in PeFLH orexin neurons as well as in paraventricular hypothalamic nucleus neurons. In summary, catecholamine neurons are required for the activation of orexin neurons during glucoprivation. Activation of orexin neurons may contribute to appetitive responses required for glucoprivic feeding.

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Year:  2015        PMID: 25978516      PMCID: PMC5393341          DOI: 10.1210/en.2015-1138

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  61 in total

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3.  Orexinergic activation of medullary premotor neurons modulates the adrenal sympathoexcitation to hypothalamic glucoprivation.

Authors:  Willian S Korim; Lama Bou Farah; Simon McMullan; Anthony J M Verberne
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4.  Neurochemical regulation of feeding in the rat: facilitation by alpha-noradrenergic, but not dopaminergic, receptor stimulants.

Authors:  S Ritter; D Wise; L Stein
Journal:  J Comp Physiol Psychol       Date:  1975-02

5.  Neurons containing orexin in the lateral hypothalamic area of the adult rat brain are activated by insulin-induced acute hypoglycemia.

Authors:  T Moriguchi; T Sakurai; T Nambu; M Yanagisawa; K Goto
Journal:  Neurosci Lett       Date:  1999-04-02       Impact factor: 3.046

6.  Differential responsiveness of dopamine-beta-hydroxylase gene expression to glucoprivation in different catecholamine cell groups.

Authors:  Ai-Jun Li; Qing Wang; Sue Ritter
Journal:  Endocrinology       Date:  2006-04-13       Impact factor: 4.736

7.  2-Deoxy-D-glucose, but not mercaptoacetate, increases food intake in decerebrate rats.

Authors:  Rebecca A Darling; Sue Ritter
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2009-06-03       Impact factor: 3.619

8.  Hindbrain catecholamine neurons mediate consummatory responses to glucoprivation.

Authors:  Bryan Hudson; Sue Ritter
Journal:  Physiol Behav       Date:  2004-09-15

9.  Glucoprivation increases expression of neuropeptide Y mRNA in hindbrain neurons that innervate the hypothalamus.

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Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2013-05-22       Impact factor: 3.619

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2.  Activation of catecholamine neurons in the ventral medulla reduces CCK-induced hypophagia and c-Fos activation in dorsal medullary catecholamine neurons.

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3.  Evidence that hindbrain astrocytes in the rat detect low glucose with a glucose transporter 2-phospholipase C-calcium release mechanism.

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6.  Selective Pharmacogenetic Activation of Catecholamine Subgroups in the Ventrolateral Medulla Elicits Key Glucoregulatory Responses.

Authors:  Ai-Jun Li; Qing Wang; Sue Ritter
Journal:  Endocrinology       Date:  2018-01-01       Impact factor: 4.736

7.  Afferent and efferent connections of C1 cells with spinal cord or hypothalamic projections in mice.

Authors:  Ruth L Stornetta; M Andrews Inglis; Kenneth E Viar; Patrice G Guyenet
Journal:  Brain Struct Funct       Date:  2015-11-11       Impact factor: 3.270

8.  Repeated Pharmacogenetic Catecholamine Neuron Activation in the Ventrolateral Medulla Attenuates Subsequent Glucoregulatory Responses.

Authors:  Ai-Jun Li; Qing Wang; Sue Ritter
Journal:  Diabetes       Date:  2020-09-29       Impact factor: 9.461

Review 9.  Central nervous system regulation of organismal energy and glucose homeostasis.

Authors:  Martin G Myers; Alison H Affinati; Nicole Richardson; Michael W Schwartz
Journal:  Nat Metab       Date:  2021-06-21

10.  NTS Catecholamine Neurons Mediate Hypoglycemic Hunger via Medial Hypothalamic Feeding Pathways.

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