scholarly journals Lactate Transport and Signaling in the Brain: Potential Therapeutic Targets and Roles in Body—Brain Interaction

2014 ◽  
Vol 35 (2) ◽  
pp. 176-185 ◽  
Author(s):  
Linda Hildegard Bergersen
Keyword(s):  
Physical Exercise ◽  
Energy Production ◽  
Brain Metabolism ◽  
Blood Stream ◽  
Cerebral Blood Vessels ◽  
Therapeutic Drugs ◽  
Brain Signals ◽  
Lactate Levels ◽  
And Function ◽  
The Brain

Lactate acts as a ‘buffer’ between glycolysis and oxidative metabolism. In addition to being exchanged as a fuel by the monocarboxylate transporters (MCTs) between cells and tissues with different glycolytic and oxidative rates, lactate may be a ‘volume transmitter’ of brain signals. According to some, lactate is a preferred fuel for brain metabolism. Immediately after brain activation, the rate of glycolysis exceeds oxidation, leading to net production of lactate. At physical rest, there is a net efflux of lactate from the brain into the blood stream. But when blood lactate levels rise, such as in physical exercise, there is net influx of lactate from blood to brain, where the lactate is used for energy production and myelin formation. Lactate binds to the lactate receptor GPR81 aka hydroxycarboxylic acid receptor (HCAR1) on brain cells and cerebral blood vessels, and regulates the levels of cAMP. The localization and function of HCAR1 and the three MCTs (MCT1, MCT2, and MCT4) expressed in brain constitute the focus of this review. They are possible targets for new therapeutic drugs and interventions. The author proposes that lactate actions in the brain through MCTs and the lactate receptor underlie part of the favorable effects on the brain resulting from physical exercise.

Influence of oxygen therapy on glucose—lactate metabolism after diffuse brain injury

2004 ◽  
Vol 101 (2) ◽  
pp. 323-329 ◽  
Author(s):  
Michael Reinert ◽  
Benoit Schaller ◽  
Hans Rudolf Widmer ◽  
Rolf Seiler ◽  
Ross Bullock
Keyword(s):  
Brain Injury ◽  
Brain Tissue ◽  
Brain Metabolism ◽  
Arterial Line ◽  
Content Type ◽  
Diffuse Brain Injury ◽  
Lactate Levels ◽  
The Brain ◽  
Fine Print ◽  
Diffuse Brain

Object. Severe traumatic brain injury (TBI) imposes a huge metabolic load on brain tissue, which can be summarized initially as a state of hypermetabolism and hyperglycolysis. In experiments O2 consumption has been shown to increase early after trauma, especially in the presence of high lactate levels and forced O2 availability. In recent clinical studies the effect of increasing O2 availability on brain metabolism has been analyzed. By their nature, however, clinical trauma models suffer from a heterogeneous injury distribution. The aim of this study was to analyze, in a standardized diffuse brain injury model, the effect of increasing the fraction of inspired O2 on brain glucose and lactate levels, and to compare this effect with the metabolism of the noninjured sham-operated brain. Methods. A diffuse severe TBI model developed by Foda and Maramarou, et al., in which a 420-g weight is dropped from a height of 2 m was used in this study. Forty-one male Wistar rats each weighing approximately 300 g were included. Anesthesized rats were monitored by placing a femoral arterial line for blood pressure and blood was drawn for a blood gas analysis. Two time periods were defined: Period A was defined as preinjury and Period B as postinjury. During Period B two levels of fraction of inspired oxygen (FiO2) were studied: air (FiO2 0.21) and oxygen (FiO2 1). Four groups were studied including sham-operated animals: air-air-sham (AAS); air-O2-sham (AOS); air-air-trauma (AAT); and air-O2-trauma (AOT). In six rats the effect of increasing the FiO2 on serum glucose and lactate was analyzed. During Period B lactate values in the brain determined using microdialysis were significantly lower (p < 0.05) in the AOT group than in the AAT group and glucose values in the brain determined using microdialysis were significantly higher (p < 0.04). No differences were demonstrated in the other groups. Increasing the FiO2 had no significant effect on the serum levels of glucose and lactate. Conclusions. Increasing the FiO2 influences dialysate glucose and lactate levels in injured brain tissue. Using an FiO2 of 1 influences brain metabolism in such a way that lactate is significantly reduced and glucose significantly increased. No changes in dialysate glucose and lactate values were found in the noninjured brain.

scholarly journals Phosphatidylserine in the brain: Metabolism and function

2014 ◽  
Vol 56 ◽  
pp. 1-18 ◽  
Author(s):  
Hee-Yong Kim ◽  
Bill X. Huang ◽  
Arthur A. Spector
Keyword(s):  
Brain Metabolism ◽  
And Function ◽  
The Brain

Cerebrovascular Dysfunction Following Sub-Failure Axial Stretch

2013 ◽  
Author(s):  
E. David Bell ◽  
Kenneth L. Monson
Keyword(s):  
Traumatic Brain Injury ◽  
Brain Injury ◽  
Cerebral Autoregulation ◽  
Mechanical Damage ◽  
Cerebral Vasculature ◽  
Cerebral Blood Vessels ◽  
Axial Stretch ◽  
Cerebrovascular Dysfunction ◽  
And Function ◽  
The Brain

Cerebral blood vessels are critical in maintaining the health and function of the brain, but their function can be disrupted by traumatic brain injury (TBI), which commonly includes damage to these vessels [1]. However, even in cases where there is not apparent mechanical damage to the cerebral vasculature, TBI can induce physiological disruptions that can lead to breakdown of the blood brain barrier or loss of cerebral autoregulation.

scholarly journals Metabolic predictors of ischemic stroke: Protein C, D-dimers, macroand microelements (review)

2020 ◽  
pp. 16-24
Author(s):  
Л.Л. Клименко ◽  
А.В. Скальный ◽  
М.Л. Благонравов ◽  
А.Н. Мазилина ◽  
М.Н. Буданова ◽  
...  
Keyword(s):  
Ischemic Stroke ◽  
Protein C ◽  
Brain Metabolism ◽  
Cerebrovascular Disorders ◽  
Coagulation System ◽  
Hematological Disorders ◽  
Multi Stage ◽  
Specific Proteins ◽  
And Function ◽  
The Brain

Гематологические нарушения и гиперкоагуляционные состояния лежат в основе механизма ишемизации мозговой ткани. На образование и структуру фибрина влияют двухвалентные ионы, что в конечном итоге приводит к изменению вязкости крови, тромбоцитозу и нарушению процесса свертывания. Изменение макро- и микроэлементного баланса служит маркером нейротрофических нарушений в работе мозга задолго до их клинических проявлений: дисбаланс металло-лигандного гомеостаза является неблагоприятным фоном для дебюта ишемического инсульта. Поэтому исследование многоступенчатых гомеостатических механизмов, обеспечивающих связь кровоснабжения мозга с его метаболизмом и функцией, является ключевым пунктом при анализе патогенетических процессов нарушения мозгового кровообращения. Высокая энергетическая потребность мозга зависит от нормального кровоснабжения и постоянной регионарной перфузии. В многофакторной системе свертывания крови ключевое место занимают специфические белки - протеин С и D-димеры, а также макро- и микроэлементы. Hematological disorders and hypercoagulability underlie the mechanism of brain ischemia. The formation and structure of fibrin are affected by divalent ions, which ultimately leads to changes in blood viscosity, thrombocytosis, and coagulopathy. Changes in the balance of macro- and microelements can predict neurotrophic disorders in the brain long before their clinical manifestation, since the disturbed metal-ligand homeostasis is an unfavorable factor for the onset of ischemic stroke. Thus, studying the multi-stage homeostatic mechanisms for the interplay of cerebral circulation and brain metabolism and function is essential for understanding the pathogenesis of cerebrovascular disorders. Normal blood supply and constant regional perfusion provide for the high brain demand for energy. Specific proteins, including protein C and D-dimers, as well as macro- and microelements, play a key role in the multifactorial coagulation system.

Biaxial and Failure Mechanical Properties of Passive Rat Middle Cerebral Arteries

2011 ◽  
Author(s):  
E. David Bell ◽  
Rahul S. Kunjir ◽  
Kenneth L. Monson
Keyword(s):  
Mechanical Properties ◽  
Traumatic Brain Injury ◽  
Cerebral Autoregulation ◽  
Cerebral Arteries ◽  
Mechanical Damage ◽  
Cerebral Vasculature ◽  
Cerebral Blood Vessels ◽  
Middle Cerebral Arteries ◽  
And Function ◽  
The Brain

Cerebral blood vessels are critical in maintaining the health and function of the brain, but their function can be disrupted by traumatic brain injury (TBI), which commonly includes damage to these vessels [1]. However, even in cases where there is not apparent mechanical damage to the cerebral vasculature, TBI can induce physiological disruptions that can lead to breakdown of the blood brain barrier or loss of cerebral autoregulation.

Nutrient control of brain neurotransmitter synthesis and function

1983 ◽  
Vol 61 (4) ◽  
pp. 271-281 ◽  
Author(s):  
G. Harvey Anderson ◽  
Janice L. Johnston
Keyword(s):  
Brain Function ◽  
Brain Metabolism ◽  
Nutrient Content ◽  
Feedback Systems ◽  
The Past ◽  
Brain Neurotransmitter ◽  
And Function ◽  
Neurotransmitter Precursors ◽  
To Receive ◽  
The Brain

The significance of normal variations in dietary and plasma nutrient content to brain metabolism and function began to receive examination in the past decade. It is now clear that the brain is much more sensitive to variations in nutrient supply than previously thought. Indeed, it seems likely that the diet-induced plasma fluctuations in nutrients, either as a result of their cofactor roles or as neurotransmitter precursors, are important components of feedback systems assisting the brain in controlling many of its functions. This discovery has suggested new approaches to understanding mechanisms controlling brain function and to treatment of diseases of the brain.

Ultrastructure of developing visual cortical synapses in the cat superior colliculus

1991 ◽  
Vol 49 ◽  
pp. 156-157
Author(s):  
Caroline A. Miller ◽  
Laura L. Bruce
Keyword(s):  
Superior Colliculus ◽  
Phosphate Buffer ◽  
Receptive Fields ◽  
Visual Cortical Area ◽  
Cortical Synapses ◽  
Visual Cortical ◽  
And Function ◽  
Phosphate Buffered Saline ◽  
The Brain ◽  
Cat Superior Colliculus

The first visual cortical axons arrive in the cat superior colliculus by the time of birth. Adultlike receptive fields develop slowly over several weeks following birth. The developing cortical axons go through a sequence of changes before acquiring their adultlike morphology and function. To determine how these axons interact with neurons in the colliculus, cortico-collicular axons were labeled with biocytin (an anterograde neuronal tracer) and studied with electron microscopy.Deeply anesthetized animals received 200-500 nl injections of biocytin (Sigma; 5% in phosphate buffer) in the lateral suprasylvian visual cortical area. After a 24 hr survival time, the animals were deeply anesthetized and perfused with 0.9% phosphate buffered saline followed by fixation with a solution of 1.25% glutaraldehyde and 1.0% paraformaldehyde in 0.1M phosphate buffer. The brain was sectioned transversely on a vibratome at 50 μm. The tissue was processed immediately to visualize the biocytin.

NON-INVASIVE BCI METHOD: EEG - ELECTROENCEPHALOGRAPHY

2019 ◽  
pp. 139-145
Author(s):  
Selma Büyükgöze
Keyword(s):  
Brain Computer Interface ◽  
Computer Interface ◽  
Electrode Placement ◽  
Eeg Signals ◽  
Non Invasive ◽  
Brain Signals ◽  
Brain States ◽  
The Brain

Brain Computer Interface consists of hardware and software that convert brain signals into action. It changes the nerves, muscles, and movements they produce with electro-physiological signs. The BCI cannot read the brain and decipher the thought in general. The BCI can only identify and classify specific patterns of activity in ongoing brain signals associated with specific tasks or events. EEG is the most commonly used non-invasive BCI method as it can be obtained easily compared to other methods. In this study; It will be given how EEG signals are obtained from the scalp, with which waves these frequencies are named and in which brain states these waves occur. 10-20 electrode placement plan for EEG to be placed on the scalp will be shown.

1805-P: Insulin Regulates a Broad Network of Gene Expression in the Brain to Regulated Brain Metabolism and Neurotransmission

Diabetes ◽  
2019 ◽  
Vol 68 (Supplement 1) ◽  
pp. 1805-P
Author(s):  
WEIKANG CAI ◽  
THIAGO M. BATISTA ◽  
RUBEN GARCIA MARTIN ◽  
ALFRED RAMIREZ ◽  
MASAHIRO KONISHI ◽  
...  
Keyword(s):  
Gene Expression ◽  
Brain Metabolism ◽  
The Brain

Molecular characterization of SARS-CoV-2

2020 ◽  
Vol 20 ◽  
Author(s):  
Miribane Dërmaku-Sopjani ◽  
Mentor Sopjani
Keyword(s):  
Public Health ◽  
Drug Targets ◽  
Virus Genome ◽  
Health Crisis ◽  
Public Health Crisis ◽  
Therapeutic Drugs ◽  
New Public Health ◽  
New Public ◽  
And Function

Abstract:: The coronavirus disease 2019 (COVID-19) is currently a new public health crisis threatening the world. This pandemic disease is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The virus has been reported to be originated in bats and by yet unknown intermediary animals were transmitted to humans in China 2019. The SARSCoV- 2 spreads faster than its two ancestors the SARS-CoV and Middle East respiratory syndrome coronavirus (MERSCoV) but has reduced fatality. At present, the SARS-CoV-2 has caused about a 1.16 million of deaths with more than 43.4 million confirmed cases worldwide, resulting in a serious threat to public health globally with yet uncertain impact. The disease is transmitted by inhalation or direct contact with an infected person. The incubation period ranges from 1 to 14 days. COVID-19 is accompanied by various symptoms, including cough, fatigue. In most people the disease is mild, but in some other people, such as in elderly and people with chronic diseases, it may progress from pneumonia to a multi-organ dysfunction. Many people are reported asymptomatic. The virus genome is sequenced, but new variants are reported. Numerous biochemical aspects of its structure and function are revealed. To date, no clinically approved vaccines and/or specific therapeutic drugs are available to prevent or treat the COVID-19. However, there are reported intensive researches on the SARSCoV- 2 to potentially identify vaccines and/or drug targets, which may help to overcome the disease. In this review, we discuss recent advances in understanding the molecular structure of SARS-CoV-2 and its biochemical characteristics.

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