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  1. Article ; Online: A pipeline for the retrieval and extraction of domain-specific information with application to COVID-19 immune signatures.

    Newton, Adam J H / Chartash, David / Kleinstein, Steven H / McDougal, Robert A

    BMC bioinformatics

    2023  Volume 24, Issue 1, Page(s) 292

    Abstract: Background: The accelerating pace of biomedical publication has made it impractical to manually, systematically identify papers containing specific information and extract this information. This is especially challenging when the information itself ... ...

    Abstract Background: The accelerating pace of biomedical publication has made it impractical to manually, systematically identify papers containing specific information and extract this information. This is especially challenging when the information itself resides beyond titles or abstracts. For emerging science, with a limited set of known papers of interest and an incomplete information model, this is of pressing concern. A timely example in retrospect is the identification of immune signatures (coherent sets of biomarkers) driving differential SARS-CoV-2 infection outcomes.
    Implementation: We built a classifier to identify papers containing domain-specific information from the document embeddings of the title and abstract. To train this classifier with limited data, we developed an iterative process leveraging pre-trained SPECTER document embeddings, SVM classifiers and web-enabled expert review to iteratively augment the training set. This training set was then used to create a classifier to identify papers containing domain-specific information. Finally, information was extracted from these papers through a semi-automated system that directly solicited the paper authors to respond via a web-based form.
    Results: We demonstrate a classifier that retrieves papers with human COVID-19 immune signatures with a positive predictive value of 86%. The type of immune signature (e.g., gene expression vs. other types of profiling) was also identified with a positive predictive value of 74%. Semi-automated queries to the corresponding authors of these publications requesting signature information achieved a 31% response rate.
    Conclusions: Our results demonstrate the efficacy of using a SVM classifier with document embeddings of the title and abstract, to retrieve papers with domain-specific information, even when that information is rarely present in the abstract. Targeted author engagement based on classifier predictions offers a promising pathway to build a semi-structured representation of such information. Through this approach, partially automated literature mining can help rapidly create semi-structured knowledge repositories for automatic analysis of emerging health threats.
    MeSH term(s) Humans ; COVID-19 ; SARS-CoV-2
    Language English
    Publishing date 2023-07-20
    Publishing country England
    Document type Journal Article
    ZDB-ID 2041484-5
    ISSN 1471-2105 ; 1471-2105
    ISSN (online) 1471-2105
    ISSN 1471-2105
    DOI 10.1186/s12859-023-05397-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Loss of function of renal Glut2 reverses hyperglycaemia and normalises body weight in mouse models of diabetes and obesity.

    de Souza Cordeiro, Leticia Maria / Bainbridge, Lauren / Devisetty, Nagavardhini / McDougal, David H / Peters, Dorien J M / Chhabra, Kavaljit H

    Diabetologia

    2022  Volume 65, Issue 6, Page(s) 1032–1047

    Abstract: Aims/hypothesis: Renal GLUT2 is increased in diabetes, thereby enhancing glucose reabsorption and worsening hyperglycaemia. Here, we determined whether loss of Glut2 (also known as Slc2a2) specifically in the kidneys would reverse hyperglycaemia and ... ...

    Abstract Aims/hypothesis: Renal GLUT2 is increased in diabetes, thereby enhancing glucose reabsorption and worsening hyperglycaemia. Here, we determined whether loss of Glut2 (also known as Slc2a2) specifically in the kidneys would reverse hyperglycaemia and normalise body weight in mouse models of diabetes and obesity.
    Methods: We used the tamoxifen-inducible CreERT2-Lox system in mice to knockout Glut2 specifically in the kidneys (Ks-Glut2 KO) to establish the contribution of renal GLUT2 to systemic glucose homeostasis in health and in insulin-dependent as well as non-insulin-dependent diabetes. We measured circulating glucose and insulin levels in response to OGTT or IVGTT under different experimental conditions in the Ks-Glut2 KO and their control mice. Moreover, we quantified urine glucose levels to explain the phenotype of the mice independently of insulin actions. We also used a transcription factor array to identify mechanisms underlying the crosstalk between renal GLUT2 and sodium-glucose cotransporter 2 (SGLT2).
    Results: The Ks-Glut2 KO mice exhibited improved glucose tolerance and massive glucosuria. Interestingly, this improvement in blood glucose control was eliminated when we knocked out Glut2 in the liver in addition to the kidneys, suggesting that the improvement is attributable to the lack of renal GLUT2. Remarkably, induction of renal Glut2 deficiency reversed hyperglycaemia and normalised body weight in mouse models of diabetes and obesity. Longitudinal monitoring of renal glucose transporters revealed that Sglt2 (also known as Slc5a2) expression was almost abolished 3 weeks after inducing renal Glut2 deficiency. To identify a molecular basis for this crosstalk, we screened for renal transcription factors that were downregulated in the Ks-Glut2 KO mice. Hnf1α (also known as Hnf1a) was among the genes most downregulated and its recovery restored Sglt2 expression in primary renal proximal tubular cells isolated from the Ks-Glut2 KO mice.
    Conclusions/interpretation: Altogether, these results demonstrate a novel crosstalk between renal GLUT2 and SGLT2 in regulating systemic glucose homeostasis via glucose reabsorption. Our findings also indicate that inhibiting renal GLUT2 is a potential therapy for diabetes and obesity.
    MeSH term(s) Animals ; Blood Glucose/metabolism ; Diabetes Mellitus, Type 2/metabolism ; Disease Models, Animal ; Female ; Glucose/metabolism ; Glucose Transporter Type 2 ; Glycosuria/metabolism ; Humans ; Hyperglycemia/metabolism ; Insulin/metabolism ; Kidney/metabolism ; Male ; Mice ; Obesity/genetics ; Obesity/metabolism ; Sodium-Glucose Transporter 2/genetics ; Sodium-Glucose Transporter 2/metabolism
    Chemical Substances Blood Glucose ; Glucose Transporter Type 2 ; Insulin ; Slc2a2 protein, mouse ; Sodium-Glucose Transporter 2 ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2022-03-15
    Publishing country Germany
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1694-9
    ISSN 1432-0428 ; 0012-186X
    ISSN (online) 1432-0428
    ISSN 0012-186X
    DOI 10.1007/s00125-022-05676-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: A Novel Approach to Assess Metabolic Flexibility Overnight in a Whole-Body Room Calorimeter.

    McDougal, David H / Marlatt, Kara L / Beyl, Robbie A / Redman, Leanne M / Ravussin, Eric

    Obesity (Silver Spring, Md.)

    2020  Volume 28, Issue 11, Page(s) 2073–2077

    Abstract: Objective: This study aimed to investigate a novel approach for determining the effects of energy-standardized dinner meals (high-fat and low-fat) on respiratory exchange ratio (RER) dynamics and metabolic flexibility.: Methods: Using a randomized ... ...

    Abstract Objective: This study aimed to investigate a novel approach for determining the effects of energy-standardized dinner meals (high-fat and low-fat) on respiratory exchange ratio (RER) dynamics and metabolic flexibility.
    Methods: Using a randomized crossover study design, energy expenditure, RER, and macronutrient oxidation rates were assessed in response to a single dinner meal during an overnight stay in a whole-body room calorimeter. Eight healthy adults completed two overnight chamber stays while fed either a high-fat (60% fat, 20% carbohydrate [CHO], 20% protein; food quotient [FQ] = 0.784) or low-fat (20% fat, 60% CHO, 20% protein; FQ = 0.899) dinner containing 40% of daily energy requirements.
    Results: Following the low-fat meal, CHO oxidation first increased before decreasing, resulting in a 12-hour RER:FQ ratio close to 1.0 (0.986 ± 0.019, P = 0.06) and therefore resulting in a 12-hour equilibrated fat balance (29 ± 76 kcal/12 hours). Following the high-fat meal, participants had a RER:FQ ratio above 1.0 (1.061 ± 0.017, P < 0.01), resulting in a significant positive 12-hour fat balance of 376 ± 142 kcal/12 hours. Various RER trajectory parameters were significantly different following the high-fat and low-fat meals.
    Conclusions: This proof-of-concept study provides an alternative approach to quantify metabolic flexibility in response to a high-fat dinner and it can be used to derive indexes of metabolic flexibility, such as the 12-hour RER:FQ ratio or the 12-hour fat balance.
    MeSH term(s) Adolescent ; Adult ; Calorimetry/methods ; Cross-Over Studies ; Energy Metabolism/physiology ; Female ; Humans ; Male ; Metabolic Flux Analysis/methods ; Young Adult
    Language English
    Publishing date 2020-09-27
    Publishing country United States
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2230457-5
    ISSN 1930-739X ; 1071-7323 ; 1930-7381
    ISSN (online) 1930-739X
    ISSN 1071-7323 ; 1930-7381
    DOI 10.1002/oby.22982
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Leptin receptor signaling is required for intact hypoglycemic counterregulation: A study in male Zucker rats.

    Morrison, Christopher D / DuVall, Marina A / Hill, Cristal M / Spann, Redin A / McDougal, David H

    Journal of diabetes and its complications

    2021  Volume 35, Issue 10, Page(s) 107994

    Abstract: Hypoglycemia is a major barrier to clinical management of persons with diabetes. Emerging evidence supports a role for leptin in gating hypoglycemic counterregulation. This work demonstrates that male leptin receptor null, Zucker (fa/fa), rats display ... ...

    Abstract Hypoglycemia is a major barrier to clinical management of persons with diabetes. Emerging evidence supports a role for leptin in gating hypoglycemic counterregulation. This work demonstrates that male leptin receptor null, Zucker (fa/fa), rats display severe impairments in hypoglycemic counterregulation. Thus, augmenting leptin levels may have clinical utility for preventing hypoglycemia.
    MeSH term(s) Animals ; Glucagon-Like Peptide-1 Receptor ; Hypoglycemia/chemically induced ; Hypoglycemia/prevention & control ; Hypoglycemic Agents/pharmacology ; Leptin/metabolism ; Male ; Obesity/complications ; Rats ; Rats, Zucker ; Receptors, Leptin/genetics
    Chemical Substances Glp1r protein, rat ; Glucagon-Like Peptide-1 Receptor ; Hypoglycemic Agents ; Leptin ; Receptors, Leptin
    Language English
    Publishing date 2021-07-15
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1105840-7
    ISSN 1873-460X ; 1056-8727
    ISSN (online) 1873-460X
    ISSN 1056-8727
    DOI 10.1016/j.jdiacomp.2021.107994
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Pipeline for retrieval of COVID-19 immune signatures

    Newton, Adam J H / Chartash, David / Kleinstein, Steven H / McDougal, Robert A

    bioRxiv

    Abstract: Objective: The accelerating pace of biomedical publication has made retrieving papers and extracting specific comprehensive scientific information a key challenge. A timely example of such a challenge is to retrieve the subset of papers that report on ... ...

    Abstract Objective: The accelerating pace of biomedical publication has made retrieving papers and extracting specific comprehensive scientific information a key challenge. A timely example of such a challenge is to retrieve the subset of papers that report on immune signatures (coherent sets of biomarkers) to understand the immune response mechanisms which drive differential SARS-CoV-2 infection outcomes. A systematic and scalable approach is needed to identify and extract COVID-19 immune signatures in a structured and machine-readable format. Materials and Methods: We used SPECTER embeddings with SVM classifiers to automatically identify papers containing immune signatures. A generic web platform was used to manually screen papers and allow anonymous submission. Results: We demonstrate a classifier that retrieves papers with human COVID-19 immune signatures with a positive predictive value of 86%. Semi-automated queries to the corresponding authors of these publications requesting signature information achieved a 31% response rate. This demonstrates the efficacy of using a SVM classifier with document embeddings of the abstract and title, to retrieve papers with scientifically salient information, even when that information is rarely present in the abstract. Additionally, classification based on the embeddings identified the type of immune signature (e.g., gene expression vs. other types of profiling) with a positive predictive value of 74%. Conclusions: Coupling a classifier based on document embeddings with direct author engagement offers a promising pathway to build a semi-structured representation of scientifically relevant information. Through this approach, partially automated literature mining can help rapidly create semi-structured knowledge repositories for automatic analysis of emerging health threats.
    Keywords covid19
    Language English
    Publishing date 2021-12-30
    Publisher Cold Spring Harbor Laboratory
    Document type Article ; Online
    DOI 10.1101/2021.12.29.474353
    Database COVID19

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  6. Article ; Online: FGF21 is required for protein restriction to extend lifespan and improve metabolic health in male mice.

    Hill, Cristal M / Albarado, Diana C / Coco, Lucia G / Spann, Redin A / Khan, Md Shahjalal / Qualls-Creekmore, Emily / Burk, David H / Burke, Susan J / Collier, J Jason / Yu, Sangho / McDougal, David H / Berthoud, Hans-Rudolf / Münzberg, Heike / Bartke, Andrzej / Morrison, Christopher D

    Nature communications

    2022  Volume 13, Issue 1, Page(s) 1897

    Abstract: Dietary protein restriction is increasingly recognized as a unique approach to improve metabolic health, and there is increasing interest in the mechanisms underlying this beneficial effect. Recent work indicates that the hormone FGF21 mediates the ... ...

    Abstract Dietary protein restriction is increasingly recognized as a unique approach to improve metabolic health, and there is increasing interest in the mechanisms underlying this beneficial effect. Recent work indicates that the hormone FGF21 mediates the metabolic effects of protein restriction in young mice. Here we demonstrate that protein restriction increases lifespan, reduces frailty, lowers body weight and adiposity, improves physical performance, improves glucose tolerance, and alters various metabolic markers within the serum, liver, and adipose tissue of wildtype male mice. Conversely, mice lacking FGF21 fail to exhibit metabolic responses to protein restriction in early life, and in later life exhibit early onset of age-related weight loss, reduced physical performance, increased frailty, and reduced lifespan. These data demonstrate that protein restriction in aging male mice exerts marked beneficial effects on lifespan and metabolic health and that a single metabolic hormone, FGF21, is essential for the anti-aging effect of this dietary intervention.
    MeSH term(s) Animals ; Diet, Protein-Restricted ; Fibroblast Growth Factors/metabolism ; Frailty/metabolism ; Hormones/metabolism ; Liver/metabolism ; Longevity ; Male ; Mice
    Chemical Substances Hormones ; fibroblast growth factor 21 ; Fibroblast Growth Factors (62031-54-3)
    Language English
    Publishing date 2022-04-07
    Publishing country England
    Document type Journal Article
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-022-29499-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: FGF21 and the Physiological Regulation of Macronutrient Preference.

    Hill, Cristal M / Qualls-Creekmore, Emily / Berthoud, Hans-Rudolf / Soto, Paul / Yu, Sangho / McDougal, David H / Münzberg, Heike / Morrison, Christopher D

    Endocrinology

    2020  Volume 161, Issue 3

    Abstract: The ability to respond to variations in nutritional status depends on regulatory systems that monitor nutrient intake and adaptively alter metabolism and feeding behavior during nutrient restriction. There is ample evidence that the restriction of water, ...

    Abstract The ability to respond to variations in nutritional status depends on regulatory systems that monitor nutrient intake and adaptively alter metabolism and feeding behavior during nutrient restriction. There is ample evidence that the restriction of water, sodium, or energy intake triggers adaptive responses that conserve existing nutrient stores and promote the ingestion of the missing nutrient, and that these homeostatic responses are mediated, at least in part, by nutritionally regulated hormones acting within the brain. This review highlights recent research that suggests that the metabolic hormone fibroblast growth factor 21 (FGF21) acts on the brain to homeostatically alter macronutrient preference. Circulating FGF21 levels are robustly increased by diets that are high in carbohydrate but low in protein, and exogenous FGF21 treatment reduces the consumption of sweet foods and alcohol while alternatively increasing the consumption of protein. In addition, while control mice adaptively shift macronutrient preference and increase protein intake in response to dietary protein restriction, mice that lack either FGF21 or FGF21 signaling in the brain fail to exhibit this homeostatic response. FGF21 therefore mediates a unique physiological niche, coordinating adaptive shifts in macronutrient preference that serve to maintain protein intake in the face of dietary protein restriction.
    MeSH term(s) Animals ; Brain/physiology ; Dietary Carbohydrates ; Dietary Proteins ; Feeding Behavior ; Fibroblast Growth Factors/physiology ; Homeostasis ; Nutrients
    Chemical Substances Dietary Carbohydrates ; Dietary Proteins ; fibroblast growth factor 21 ; Fibroblast Growth Factors (62031-54-3)
    Language English
    Publishing date 2020-02-19
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 427856-2
    ISSN 1945-7170 ; 0013-7227
    ISSN (online) 1945-7170
    ISSN 0013-7227
    DOI 10.1210/endocr/bqaa019
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Chromosome-level assembly of the

    Cox, Murray P / Guo, Yanan / Winter, David J / Sen, Diya / Cauldron, Nicholas C / Shiller, Jason / Bradley, Ellie L / Ganley, Austen R / Gerth, Monica L / Lacey, Randy F / McDougal, Rebecca L / Panda, Preeti / Williams, Nari M / Grunwald, Niklaus J / Mesarich, Carl H / Bradshaw, Rosie E

    Frontiers in microbiology

    2022  Volume 13, Page(s) 1038444

    Abstract: ... ...

    Abstract Phytophthora
    Language English
    Publishing date 2022-11-02
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587354-4
    ISSN 1664-302X
    ISSN 1664-302X
    DOI 10.3389/fmicb.2022.1038444
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Autonomic control of the eye.

    McDougal, David H / Gamlin, Paul D

    Comprehensive Physiology

    2015  Volume 5, Issue 1, Page(s) 439–473

    Abstract: The autonomic nervous system influences numerous ocular functions. It does this by way of parasympathetic innervation from postganglionic fibers that originate from neurons in the ciliary and pterygopalatine ganglia, and by way of sympathetic innervation ...

    Abstract The autonomic nervous system influences numerous ocular functions. It does this by way of parasympathetic innervation from postganglionic fibers that originate from neurons in the ciliary and pterygopalatine ganglia, and by way of sympathetic innervation from postganglionic fibers that originate from neurons in the superior cervical ganglion. Ciliary ganglion neurons project to the ciliary body and the sphincter pupillae muscle of the iris to control ocular accommodation and pupil constriction, respectively. Superior cervical ganglion neurons project to the dilator pupillae muscle of the iris to control pupil dilation. Ocular blood flow is controlled both via direct autonomic influences on the vasculature of the optic nerve, choroid, ciliary body, and iris, as well as via indirect influences on retinal blood flow. In mammals, this vasculature is innervated by vasodilatory fibers from the pterygopalatine ganglion, and by vasoconstrictive fibers from the superior cervical ganglion. Intraocular pressure is regulated primarily through the balance of aqueous humor formation and outflow. Autonomic regulation of ciliary body blood vessels and the ciliary epithelium is an important determinant of aqueous humor formation; autonomic regulation of the trabecular meshwork and episcleral blood vessels is an important determinant of aqueous humor outflow. These tissues are all innervated by fibers from the pterygopalatine and superior cervical ganglia. In addition to these classical autonomic pathways, trigeminal sensory fibers exert local, intrinsic influences on many of these regions of the eye, as well as on some neurons within the ciliary and pterygopalatine ganglia.
    MeSH term(s) Accommodation, Ocular/physiology ; Animals ; Autonomic Nervous System/physiology ; Eye/blood supply ; Eye/innervation ; Humans ; Intraocular Pressure/physiology ; Neural Pathways/physiology ; Pupil/physiology ; Reflex/physiology ; Regional Blood Flow/physiology ; Trigeminal Nerve/physiology
    Language English
    Publishing date 2015-01
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Review
    ISSN 2040-4603
    ISSN (online) 2040-4603
    DOI 10.1002/cphy.c140014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Response of catecholaminergic neurons in the mouse hindbrain to glucoprivic stimuli is astrocyte dependent.

    Rogers, Richard C / McDougal, David H / Ritter, Sue / Qualls-Creekmore, Emily / Hermann, Gerlinda E

    American journal of physiology. Regulatory, integrative and comparative physiology

    2018  Volume 315, Issue 1, Page(s) R153–R164

    Abstract: ... depends on hindbrain astrocyte glucose sensors (McDougal DH, Hermann GE, Rogers RC. Front Neurosci 7: 249 ...

    Abstract Hindbrain catecholaminergic (CA) neurons are required for critical autonomic, endocrine, and behavioral counterregulatory responses (CRRs) to hypoglycemia. Recent studies suggest that CRR initiation depends on hindbrain astrocyte glucose sensors (McDougal DH, Hermann GE, Rogers RC. Front Neurosci 7: 249, 2013; Rogers RC, Ritter S, Hermann GE. Am J Physiol Regul Integr Comp Physiol 310: R1102-R1108, 2016). To test the proposition that hindbrain CA responses to glucoprivation are astrocyte dependent, we utilized transgenic mice in which the calcium reporter construct (GCaMP5) was expressed selectively in tyrosine hydroxylase neurons (TH-GCaMP5). We conducted live cell calcium-imaging studies on tissue slices containing the nucleus of the solitary tract (NST) or the ventrolateral medulla, critical CRR initiation sites. Results show that TH-GCaMP5 neurons are robustly activated by a glucoprivic challenge and that this response is dependent on functional astrocytes. Pretreatment of hindbrain slices with fluorocitrate (an astrocytic metabolic suppressor) abolished TH-GCaMP5 neuronal responses to glucoprivation, but not to glutamate. Pharmacologic results suggest that the astrocytic connection with hindbrain CA neurons is purinergic via P2 receptors. Parallel imaging studies on hindbrain slices of NST from wild-type C57BL/6J mice, in which astrocytes and neurons were prelabeled with a calcium reporter dye and an astrocytic vital dye, show that both cell types are activated by glucoprivation but astrocytes responded significantly sooner than neurons. Pretreatment of these hindbrain slices with P2 antagonists abolished neuronal responses to glucoprivation without interruption of astrocyte responses; pretreatment with fluorocitrate eliminated both astrocytic and neuronal responses. These results support earlier work suggesting that the primary detection of glucoprivic signals by the hindbrain is mediated by astrocytes.
    MeSH term(s) Animals ; Astrocytes/metabolism ; Calcium Signaling ; Catecholamines/metabolism ; Female ; Genes, Reporter ; Glucose/deficiency ; Glutamic Acid/metabolism ; Immunohistochemistry ; In Vitro Techniques ; Male ; Mice, Inbred C57BL ; Mice, Transgenic ; Microscopy, Confocal ; Neurons/metabolism ; Receptors, Purinergic P2/metabolism ; Rhombencephalon/cytology ; Rhombencephalon/metabolism ; Time Factors ; Tyrosine 3-Monooxygenase/metabolism
    Chemical Substances Catecholamines ; Receptors, Purinergic P2 ; Glutamic Acid (3KX376GY7L) ; Tyrosine 3-Monooxygenase (EC 1.14.16.2) ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2018-03-28
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 603839-6
    ISSN 1522-1490 ; 0363-6119
    ISSN (online) 1522-1490
    ISSN 0363-6119
    DOI 10.1152/ajpregu.00368.2017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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