Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 6

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Traumatic brain injury extending to the striatum alters autonomic thermoregulation and hypothalamic monoamines in recovering rats

Verduzco-Mendoza, Antonio, Mota-Rojas, Daniel, Olmos Hernández, Silvia Adriana, Gálvez-Rosas, Arturo, Aguirre-Pérez, Alexander, Cortes-Altamirano, José Luis, Alfaro-Rodríguez, Alfonso, Parra-Cid, Carmen, Avila-Luna, Alberto, Bueno-Nava, Antonio·2023·Frontiers in Neuroscience

Abstract

The brain cortex is the structure that is typically injured in traumatic brain injury (TBI) and is anatomically connected with other brain regions, including the striatum and hypothalamus, which are associated in part with motor function and the regulation of body temperature, respectively. We investigated whether a TBI extending to the striatum could affect peripheral and core temperatures as an indicator of autonomic thermoregulatory function. Moreover, it is unknown whether thermal modulation is accompanied by hypothalamic and cortical monoamine changes in rats with motor function recovery. The animals were allocated into three groups: the sham group (sham), a TBI group with a cortical contusion alone (TBI alone), and a TBI group with an injury extending to the dorsal striatum (TBI + striatal injury). Body temperature and motor deficits were evaluated for 20 days post-injury. On the 3rd and 20th days, rats were euthanized to measure the serotonin (5-HT), noradrenaline (NA), and dopamine (DA) levels using high-performance liquid chromatography (HPLC). We observed that TBI with an injury extending to the dorsal striatum increased core and peripheral temperatures. These changes were accompanied by a sustained motor deficit lasting for 14 days. Furthermore, there were notable increases in NA and 5-HT levels in the brain cortex and hypothalamus both 3 and 20 days after injury. In contrast, rats with TBI alone showed no changes in peripheral temperatures and achieved motor function recovery by the 7th day post-injury. In conclusion, our results suggest that TBI with an injury extending to the dorsal striatum elevates both core and peripheral temperatures, causing a delay in functional recovery and increasing hypothalamic monoamine levels. The aftereffects can be attributed to the injury site and changes to the autonomic thermoregulatory functions.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.3389/fnins.2023.1304440

Cites

9 of 9 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Research works printed but not linked: 99

  1. Adèr, 1980, Bilaterally diverging axon collaterals and contralateral projections from rat locus coeruleus neurons, demonstrated by fluorescent retrograde double labeling and norepinephrine metabolism, J. Neural Transm., 49, 207, 10.1007/BF01252126 · DOI
  2. Albin, 1989, The functional-anatomy of basal ganglia disorders, Trends Neurosci., 12, 366, 10.1016/0166-2236(89)90074-X · DOI · Paper page
  3. Atkins, 2017, Is temperature an important variable in recovery after mild traumatic brain injury?, F1000Res, 6, 2031, 10.12688/f1000research.12025.1 · DOI
  4. Avila-Luna, 2018, Dopamine D1 receptor activation maintains motor coordination in injured rats but does not accelerate the recovery of the motor coordination deficit, Behav. Brain Res., 336, 145, 10.1016/j.bbr.2017.08.026 · DOI
  5. Avila-Luna, 2016, Effects of dopamine D-1 receptor activation and blockade on dopamine and noradrenaline levels in the rat brain, Neurosci. Lett., 612, 116, 10.1016/j.neulet.2015.11.040 · DOI
  6. Bao, 2021, Iatrogenic hypothalamus injury after resection of Subependymoma within the left brain ventricle, Cureus, 13, e13044, 10.7759/cureus.13044 · DOI
  7. Björklund, 2007, Dopamine neuron systems in the brain: an update, Trends Neurosci., 30, 194, 10.1016/j.tins.2007.03.006 · DOI · Paper page
  8. Bolam, 2016, Histamine and the striatum, Neuropharmacology, 106, 74, 10.1016/j.neuropharm.2015.08.013 · DOI
  9. Boulant, 2006, Neuronal basis of Hammel's model for set-point thermoregulation, J. Appl. Physiol., 100, 1347, 10.1152/japplphysiol.01064.2005 · DOI
  10. Boursin, 2018, Semantics, epidemiology and semiology of stroke, Soins, 63, 24, 10.1016/j.soin.2018.06.008 · DOI
  11. Boyeson, 1992, Cerebellar norepinephrine infusions facilitate recovery after sensorimotor cortex injury, Brain Res. Bull., 29, 435, 10.1016/0361-9230(92)90080-H · DOI
  12. Brailowsky, 1986, Gamma-aminobutyric acid-induced potentiation of cortical hemiplegia, Brain Res., 362, 322, 10.1016/0006-8993(86)90457-9 · DOI
  13. Bricknell, 1997, An evaluation of infra-red tympanic thermometry for thermal physiology research, J. R. Army Med. Corps, 143, 149, 10.1136/jramc-143-03-04 · DOI
  14. Bueno-Nava, 2010, Recovery of motor deficit, cerebellar serotonin and lipid peroxidation levels in the cortex of injured rats, Neurochem. Res., 35, 1538, 10.1007/s11064-010-0213-4 · DOI
  15. Bueno-Nava, 2008, Reversal of noradrenergic depletion and lipid peroxidation in the pons after brain injury correlates with motor function recovery in rats, Neurosci. Lett., 443, 32, 10.1016/j.neulet.2008.07.046 · DOI
  16. Carr, 2013, Inflammation, Cerebral Vasospasm, and Evolving Theories of Delayed Cerebral Ischemia, Neurol. Res. Int., 2013, 506584, 10.1155/2013/506584 · DOI
  17. Childs, 2008, Human brain temperature: regulation, measurement and relationship with cerebral trauma: part 1, Br. J. Neurosurg., 22, 486, 10.1080/02688690802245541 · DOI
  18. Clark, 1986, Changes in body temperature after administration of adrenergic and serotonergic agents and related drugs including antidepressants: II, Neurosci. Biobehav. Rev., 10, 153, 10.1016/0149-7634(86)90025-4 · DOI
  19. Coon, 2018, Chapter 43—thermoregulation in Parkinson disease, 715
  20. Cooper, 2002, Some historical perspectives on thermoregulation, J. Appl. Physiol., 92, 1717, 10.1152/japplphysiol.01051.2001 · DOI
  21. Cooper, 1976, The effect of noradrenaline, injected into the hypothalamus, on thermoregulation in the cat, J. Physiol., 261, 211, 10.1113/jphysiol.1976.sp011554 · DOI
  22. Costa, 2006, Rapid alterations in corticostriatal ensemble coordination during acute dopamine-dependent motor dysfunction, Neuron, 52, 359, 10.1016/j.neuron.2006.07.030 · DOI · Paper page
  23. Cox, 1980, A dopamine-5-hydroxytryptamine link in the hypothalamic pathways which mediate heat loss in the rat, J. Physiol., 303, 9, 10.1113/jphysiol.1980.sp013266 · DOI
  24. De Jonge, 2018, Fever worsens outcomes in animal models of ischaemic stroke: a systematic review and meta-analysis, Eur. Stroke J., 4, 29, 10.1177/2396987318776421 · DOI
  25. Dietrich, 2007, Hyperthermia and central nervous system injury, 201
  26. Ding, 2008, Corticostriatal and thalamostriatal synapses have distinctive properties, J. Neurosci., 28, 6483, 10.1523/JNEUROSCI.0435-08.2008 · DOI · Paper page
  27. Dougherty, 2020, Catecholaminergic axons in the neocortex of adult mice regrow following brain injury, Exp. Neurol., 323, 113089, 10.1016/j.expneurol.2019.113089 · DOI
  28. El Bitar, 2014, Thermoregulatory vasomotor tone of the rat tail and paws in thermoneutral conditions and its impact on a behavioral model of acute pain, J. Neurophysiol., 112, 2185, 10.1152/jn.00721.2013 · DOI
  29. Fealey, 2013, Chapter 7—Interoception and autonomic nervous system reflexes thermoregulation, 79
  30. Feldberg, 1963, A new concept of temperature regulation by amines in the hypothalamus, Nature, 200, 1325, 10.1038/2001325a0 · DOI
  31. Feldman, 1966, Striatal connections and influences on somatosensory and photic projections to the hypothalamus, Electroencephalogr. Clin. Neurophysiol., 21, 249, 10.1016/0013-4694(66)90074-5 · DOI
  32. Franklin, 1993, The influence of thermoregulatory mechanisms on post-exercise hypotension in humans, J. Physiol., 470, 231, 10.1113/jphysiol.1993.sp019856 · DOI
  33. Gaither, 2015, Environmental hyperthermia in prehospital patients with major traumatic brain injury, J. Emerg. Med., 49, 375, 10.1016/j.jemermed.2015.01.038 · DOI
  34. Gálvez-Rosas, 2019, GABAergic imbalance is normalized by dopamine D1 receptor activation in the striatum contralateral to the cortical injury in motor deficit-recovered rats, Psychopharmacology (Berl), 236, 2211, 10.1007/s00213-019-05215-1 · DOI
  35. García-Díaz, 2023, Alpha2-adrenergic receptor activation reinstates motor deficits in rats recovering from cortical injury, Neural Regen. Res., 18, 875, 10.4103/1673-5374.353501 · DOI
  36. Geffroy, 2004, Severe traumatic head injury in adults: which patients are at risk of early hyperthermia?, Intensive Care Med., 30, 785, 10.1007/s00134-004-2280-y · DOI
  37. Giner, 2022, Traumatic brain injury in the new millennium: new population and new management, Neurologia, 37, 383, 10.1016/j.nrleng.2019.03.024 · DOI
  38. Gonzalez, 1986, Different roles of intrahypothalamic and nigrostriatal dopaminergic systems in thermoregulatory responses of the rat, Life Sci., 39, 707, 10.1016/0024-3205(86)90018-4 · DOI
  39. Gouma, 2012, A simple procedure for estimation of total body surface area and determination of a new value of Meeh's constant in rats, Lab Anim., 46, 40, 10.1258/la.2011.011021 · DOI
  40. Gowda, 2018, Thermoregulation in brain injury, 789
  41. Graybiel, 1979, Fiber connections of the basal ganglia, 239
  42. Grillner, 2016, The basal ganglia over 500 million years, Curr. Biol., 26, R1088, 10.1016/j.cub.2016.06.041 · DOI · Paper page
  43. Guzik, 2017, Stroke epidemiology and risk factor management, Continuum, 23, 15, 10.1212/CON.0000000000000416 · DOI · Paper page
  44. Haarbauer-Krupa, 2021, Epidemiology of chronic effects of traumatic brain injury, J. Neurotrauma, 38, 3235, 10.1089/neu.2021.0062 · DOI · Paper page
  45. Haber, 2016, Corticostriatal circuitry, Dialogues Clin. Neurosci., 18, 7, 10.31887/DCNS.2016.18.1/shaber · DOI · Paper page
  46. Harting, 2006, Oculomotor-related pathways of the basal ganglia, 441
  47. Heym, 1982, Serotonergic innervation of the lateral hypothalamus: evidence from synaptosomal uptake studies, Brain Res. Bull., 8, 131, 10.1016/0361-9230(82)90039-9 · DOI
  48. Hutson, 2011, Traumatic brain injury in adult rats causes progressive nigrostriatal dopaminergic cell loss and enhanced vulnerability to the pesticide paraquat, J. Neurotrauma, 28, 1783, 10.1089/neu.2010.1723 · DOI
  49. Jenkins, 2018, Dopaminergic abnormalities following traumatic brain injury, Brain, 141, 797, 10.1093/brain/awx357 · DOI
  50. Jenkins, 2016, Catecholamines and cognition after traumatic brain injury, Brain, 139, 2345, 10.1093/brain/aww128 · DOI
  51. Kandel, 2013, Principles of neural science
  52. Kremkow, 2018, Thalamocortical circuits and functional architecture, Annual Rev Vis Sci, 4, 263, 10.1146/annurev-vision-091517-034122 · DOI
  53. Krobert, 1994, Spontaneous and amphetamine-evoked release of cerebellar noradrenaline after sensorimotor cortex contusion: an in vivo microdialysis study in the awake rat, J. Neurochem., 62, 2233, 10.1046/j.1471-4159.1994.62062233.x · DOI
  54. Kullmann, 2021, Chapter 7—resting-state functional connectivity of the human hypothalamus, 113
  55. Laird-Hopkins, 2023, Thermoregulatory ability and mechanism do not differ consistently between neotropical and temperate butterflies, Glob. Chang. Biol., 29, 4180, 10.1111/gcb.16797 · DOI
  56. Lezama-García, 2022, Transient receptor potential (TRP) and thermoregulation in animals: structural biology and neurophysiological aspects, Animals, 12, 106, 10.3390/ani12010106 · DOI
  57. Liljeholm, 2012, Contributions of the striatum to learning, motivation, and performance: an associative account, Trends Cogn. Sci., 16, 467, 10.1016/j.tics.2012.07.007 · DOI · Paper page
  58. Lin, 1983, Serotonergic mechanisms in the hypothalamus mediate thermoregulatory responses in rats, Naunyn Schmiedebergs Arch. Pharmacol., 322, 271, 10.1007/BF00508342 · DOI
  59. Mcgregor, 2019, Circuit mechanisms of Parkinson’s disease, Neuron, 101, 1042, 10.1016/j.neuron.2019.03.004 · DOI · Paper page
  60. Morrison, 2019, Central mechanisms for thermoregulation, Annu. Rev. Physiol., 81, 285, 10.1146/annurev-physiol-020518-114546 · DOI · Paper page
  61. Mota-Rojas, 2021, Physiological and behavioral mechanisms of thermoregulation in mammals, Animals, 11, 1733, 10.3390/ani11061733 · DOI
  62. Mrozek, 2012, Brain temperature: physiology and pathophysiology after brain injury, Anesthesiol Res Pract, 2012, 1, 10.1155/2012/989487 · DOI
  63. Nakamura, 2018, Chapter 16—afferent pathways for autonomic and shivering thermoeffectors, 263
  64. 2001, Especificaciones técnicas para la producción, cuidado y uso de los animales de laboratorio
  65. Nomoto, 2004, Role of afferent pathways of heat and cold in body temperature regulation, Int. J. Biometeorol., 49, 67, 10.1007/s00484-004-0220-8 · DOI
  66. Osier, 2016, The controlled cortical impact model of experimental brain trauma: overview, research applications, and protocol, 177, 10.1007/978-1-4939-3816-2_11 · DOI
  67. Osier, 2016, The controlled cortical impact model: applications, considerations for researchers, and future directions, Front. Neurol., 7, 134, 10.3389/fneur.2016.00134 · DOI
  68. Paxinos, 2013, The rat brain in stereotaxic coordinates
  69. Pegoli, 2020, Temperature management in acute brain injury: a systematic review of clinical evidence, Clin. Neurol. Neurosurg., 197, 106165, 10.1016/j.clineuro.2020.106165 · DOI
  70. Rabinstein, 2007, Non-infectious fever in the neurological intensive care unit: incidence, causes and predictors, J. Neurol. Neurosurg. Psychiatry, 78, 1278, 10.1136/jnnp.2006.112730 · DOI
  71. Ramos-Languren, 2021, Glutamate, glutamine, GABA and oxidative products in the pons following cortical injury and their role in motor functional recovery, Neurochem. Res., 46, 3179, 10.1007/s11064-021-03417-8 · DOI
  72. Ramos-Languren, 2016, Sensorimotor intervention recovers noradrenaline content in the dentate gyrus of cortical injured rats, Neurochem. Res., 41, 3261, 10.1007/s11064-016-2054-2 · DOI
  73. Rand, 1965, The tail of the rat, in temperature regulation and acclimatization, Can. J. Physiol. Pharmacol., 43, 257, 10.1139/y65-025 · DOI
  74. Reppucci, 2016, Organization of connections between the amygdala, medial prefrontal cortex, and lateral hypothalamus: a single and double retrograde tracing study in rats, Brain Struct. Funct., 221, 2937, 10.1007/s00429-015-1081-0 · DOI
  75. Rincon, 2014, The epidemiology of spontaneous fever and hypothermia on admission of brain injury patients to intensive care units: a multicenter cohort study: clinical article, J. Neurosurg., 121, 950, 10.3171/2014.7.JNS132470 · DOI
  76. Risold, 1997, The structural organization of connections between hypothalamus and cerebral cortex1Published on the world wide web on 2 June 1997.1, Brain Res. Rev., 24, 197, 10.1016/S0165-0173(97)00007-6 · DOI · Paper page
  77. Robinson, 1980, Time course of changes in catecholamines following right hemispheric cerebral infarction in the rat, Brain Res., 181, 202, 10.1016/0006-8993(80)91271-8 · DOI
  78. Rockland, 2019, Corticothalamic axon morphologies and network architecture, Eur. J. Neurosci., 49, 969, 10.1111/ejn.13910 · DOI
  79. Rossi, 2001, Brain temperature, body core temperature, and intracranial pressure in acute cerebral damage, J. Neurol. Neurosurg. Psychiatry, 71, 448, 10.1136/jnnp.71.4.448 · DOI · Paper page
  80. Saini, 2021, Global epidemiology of stroke and access to acute ischemic stroke interventions, Neurology, 97, S6, 10.1212/WNL.0000000000012781 · DOI · Paper page
  81. Saper, 2000, Hypothalamic connections with the cerebral cortex, 39
  82. Shin, 2011, Traumatic brain injury reduces striatal tyrosine hydroxylase activity and potassium-evoked dopamine release in rats, Brain Res., 1369, 208, 10.1016/j.brainres.2010.10.096 · DOI
  83. Skok, 2021, Thermoregulation: a journey from physiology to computational models and the intensive care unit, Wiley Interdiscip. Rev. Syst. Biol. Med., 13, e1513, 10.1002/wsbm.1513 · DOI
  84. Škop, 2020, The contribution of the mouse tail to thermoregulation is modest, Am. J. Physiol. Endocrinol. Metab., 319, E438, 10.1152/ajpendo.00133.2020 · DOI
  85. Surmeier, 2017, Selective neuronal vulnerability in Parkinson disease, Nat. Rev. Neurosci., 18, 101, 10.1038/nrn.2016.178 · DOI · Paper page
  86. Svedung Wettervik, 2021, Systemic hyperthermia in traumatic brain injury—relation to intracranial pressure dynamics, cerebral energy metabolism, and clinical outcome, J. Neurosurg. Anesthesiol., 33, 329, 10.1097/ANA.0000000000000695 · DOI
  87. Takada, 1986, Collateral projections from the substantia nigra to the cingulate cortex and striatum in the rat, Brain Res., 380, 331, 10.1016/0006-8993(86)90230-1 · DOI
  88. Takahashi, 2015, Chapter 34—autonomic dysfunction syndromes after acute brain injury, 539
  89. Thompson, 2005, Development of posttraumatic hyperthermia after traumatic brain injury in rats is associated with increased periventricular inflammation, J. Cereb. Blood Flow Metab., 25, 163, 10.1038/sj.jcbfm.9600008 · DOI
  90. Thompson, 2007, Intensive care unit management of fever following traumatic brain injury, Intensive Crit. Care Nurs., 23, 91, 10.1016/j.iccn.2006.11.005 · DOI
  91. Thompson, 2003, Hyperthermia following traumatic brain injury: a critical evaluation, Neurobiol. Dis., 12, 163, 10.1016/S0969-9961(02)00030-X · DOI
  92. Triggs, 1984, In vivo lipid-peroxidation in rat-brain following intracortical Fe-2+ injection, J. Neurochem., 42, 976, 10.1111/j.1471-4159.1984.tb12699.x · DOI
  93. Van Bockstaele, 1993, Topography of serotonin neurons in the dorsal raphe nucleus that send axon collaterals to the rat prefrontal cortex and nucleus accumbens, Brain Res., 624, 188, 10.1016/0006-8993(93)90077-Z · DOI · Paper page
  94. Verduzco-Mendoza, Experimental applications and factors involved in validating thermal windows using infrared thermography to assess the health and Thermostability of laboratory animals, Animals, 11, 3448, 10.3390/ani11123448 · DOI
  95. Verduzco-Mendoza, Role of the dopaminergic system in the striatum and its association with functional recovery or rehabilitation after brain injury, Front. Neurosci., 15, 3404, 10.3389/fnins.2021.693404 · DOI
  96. Vitrac, 2017, Monoaminergic modulation of motor cortex function, Front Neural Circuits, 11, 72, 10.3389/fncir.2017.00072 · DOI
  97. Walter, 2016, The pathophysiological basis and consequences of fever, Crit. Care, 20, 200, 10.1186/s13054-016-1375-5 · DOI · Paper page
  98. Yahya, 2021, The basal ganglia corticostriatal loops and conditional learning, Rev. Neurosci., 32, 181, 10.1515/revneuro-2020-0047 · DOI
  99. Zakhary, 2017, Bromocriptine in central hyperthermia after severe traumatic brain injury, Open J Emerg Med, 5, 102, 10.4236/ojem.2017.53010 · DOI

Metadata

Authors
Verduzco-Mendoza, A., Mota-Rojas, D., Olmos Hernández, S. A., Gálvez-Rosas, A., Aguirre-Pérez, A., Cortes-Altamirano, J. L., Alfaro-Rodríguez, A., Parra-Cid, C., Avila-Luna, A., & Bueno-Nava, A.
Venue
Frontiers in Neuroscience
Published
2023-12-07
Volume
17
ISSN
1662-453X
Cited by
6
References
9

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.