The Comparative Anatomy of the Frontal Lobe, and its Bearing upon the Pathology of Insanity

1911 ◽  
Vol 57 (236) ◽  
pp. 52-55 ◽  
Author(s):  
Sydney J. Cole
Keyword(s):  
Cerebral Cortex ◽  
Frontal Cortex ◽  
Frontal Lobe ◽  
Comparative Anatomy ◽  
Late Development ◽  
Naked Eye ◽  
Prefrontal Region ◽  
The Brain ◽  
Comparative Histology ◽  
Great Development

Dr. J. S. Bolton has shown that in dementia the seat of greatest wasting of the cerebral cortex is commonly the prefrontal region, a region which (following Flechsig) he regards as a centre of higher association, the great development of which constitutes a leading character of the brain of man. This is a region which in man is one of the latest to myelinate (thirty-fifth in order, according to Flechsig), and if the order of myelination, as a part of ontogeny, may be taken as an approximate recapitulation of the order of phylogeny, then we might infer that the prefrontal region of man is a new region, of late development, absent or poorly developed in animals lower than man. Upon this assumption the predominant wasting of this region in dementia would be readily explained in accordance with Hughlings Jackson's doctrine of evolution and dissolution—dissolution following the inverse order of evolution. For an understanding of the pathology of insanity it is obviously important to inquire how far a study of comparative anatomy, especially of the primates, lends any support to such a conception. The aim of my discourse is accordingly to present, first, a brief survey of the recent observations of Dr. K. Brodmann, of Berlin, upon the comparative histology of the frontal cortex, and then some observations of my own upon naked-eye anatomy of the brain of man and higher apes.

Editorial introduction to Greenwood/West dialogue

2000 ◽  
Vol 6 (6) ◽  
pp. 704-704
Author(s):  
JASON BRANDT
Keyword(s):  
Anorexia Nervosa ◽  
Prefrontal Cortex ◽  
Pathological Gambling ◽  
Frontal Cortex ◽  
Frontal Lobe ◽  
Editorial Introduction ◽  
Frontal Lobe Dysfunction ◽  
The Brain ◽  
Artistic Skill

Although a U.S. Presidential Proclamation designated the 1990s “The Decade of the Brain,” not all cerebral constituents shared equally in the limelight. By anyone's accounting, the prefrontal cortex was the darling of clinicians and neuroscientists throughout the '90s, with everything from schizophrenia and anorexia nervosa to pathological gambling and the emergence of artistic skill attributed to “frontal lobe dysfunction” (David, 1992; Miller et al., 1998; Rugle & Melamed, 1993). It should come as no surprise, then, that that most universal of cognitive afflictions, aging, should be linked to changes in frontal cortex.

scholarly journals The effect of transcranial electrostimulation on the frontal crust of students during a psychoemotional stress

2020 ◽  
Vol 24 (1) ◽  
pp. 75-84
Author(s):  
Azamat Halidovich Kade ◽  
Caida Kazbekovna Ahejak-Naguze ◽  
Viktor Vladimirovich Durov ◽  
Yulia Viktorovna Kashina ◽  
Elena Genadevna Tacenko ◽  
...  
Keyword(s):  
Cerebral Cortex ◽  
Electrical Stimulation ◽  
Frontal Cortex ◽  
Stress Resistance ◽  
Frontal Region ◽  
Transcranial Electrical Stimulation ◽  
Stress Effect ◽  
Psychoemotional Stress ◽  
Before And After ◽  
The Brain

Relevance: transcranial electrical stimulation has an anti-stress effect in humans. One of the possible mechanisms is due to changes in the functional state of the frontal region of the cerebral cortex.The aim: to evaluate the dynamics of tractography of the frontal region of the human cerebral cortex during psychoemotional stress before and after transcranial electrical stimulation. Materials and methods: Observations were performed on 26 conditionally healthy young men. Students assessed the level of stress resistance by N.N. Kirsheva, N.V. Ryabchikova and heart rate variability in the test period. Brain MRI was performed on a high-field tomograph (magnetic field strength 3 T) from General Electric (USA), followed by software processing and tractography. 16 subjects (main group) underwent transcranial electrical stimulation (TES) therapy. TES therapy was performed using the TRANSAIR-02 apparatus with monopolar impulses. Sessions were held in the evening from 18 to 22 hours every other day. The course consisted of 5 sessions of 30 minutes, the current strength was from 2.0 to 3.0 mA After a course of TES therapy, MRI of the brain and tractography were repeated. In the comparison group (10 people), TES therapy was not performed, but MRI and tractography were similarly repeated. The tractograms compared the area of the tracts in the frontal region of the cerebral cortex in both groups, as well as before and after TES therapy. For statistical analysis of the results of the study used the program: “STATISTICA 10”. Results: On the tractograms of the frontal cortex of the brain, in students experiencing stress due to the training load in the crediting period, the tract area on the tractogram was 7.9 ± 0.4 cm2. After 5 sessions of transcranial electrical stimulation, the level of stress resistance increased. On the tractograms of the frontal cortex, the area of the tracts increased and amounted to 13.4 ± 0.5 cm2.The conclusion: After transcranial electrical stimulation, when psychoemotional stress is removed, students restore paths in the frontal region of the cerebral cortex

scholarly journals Iron Deposition in the Brain Following the Ischemia in a Rat Model of Ischemic Tolerance

2004 ◽  
Vol 47 (4) ◽  
pp. 285-288 ◽  
Author(s):  
Viera Danielisová ◽  
Miroslava Némethová ◽  
Jozef Burda
Keyword(s):  
Cerebral Cortex ◽  
Frontal Cortex ◽  
Rat Model ◽  
Pyramidal Neurons ◽  
Pyramidal Cells ◽  
Ischemic Tolerance ◽  
Iron Deposition ◽  
Sham Operation ◽  
Vessel Occlusion ◽  
The Brain

Preconditioning of the brain by short-term ischemia increases brain tolerance to the subsequent severer ischemia. In this study, we investigated iron deposition in the cerebral cortex and the ischemic tolerance in a rat model of cerebral ischemia. Forebrain ischemia was induced by four-vessel occlusion for 5 min as ischemic preconditioning. Two days after preconditioning or after the sham-operation, the second ischemia was induced for 20 min. Changes in the cerebral cortex were examined after 1 to 8 weeks of recirculation following 20 min ischemia with or without preconditioning using the iron histochemistry. Granular deposits of the iron were found in the cytoplasm of the pyramidal cells in the layers III and V of the frontal cortex after 1 week of recirculation. When the rats were exposed to 5 min ischemia 2 days before 20 min lasting ischemia, the deposition of iron in the cytoplasm of the pyramidal cells in layers III and V of the frontal cortex was significantly lower during all periods of reperfusion. Preconditioning 5 min ischemia followed by 2 days of reperfusion before 20 min ischemia also prevented degeneration of the pyramidal neurons in layers III and V of the frontal cortex.

scholarly journals The brain of Gadus, with special reference to the medulla oblongata and its variations according to the feeding habits of different gadidæ—I

1935 ◽  
Vol 117 (805) ◽  
pp. 367-399 ◽  
Keyword(s):  
Special Reference ◽  
Medulla Oblongata ◽  
Feeding Habits ◽  
Stomach Contents ◽  
Dorsal Surface ◽  
Naked Eye ◽  
Definite Manner ◽  
Rhomboid Fossa ◽  
The Brain ◽  
Great Development

In a previous paper (Evans, 1932) we have described the medulla oblongata of the Cyprinidae and have shown that the pattern of the medulla varies according to the habits of feeding, so that it was possible to divide the Cyprinidae into four groups. We propose to attempt a similar study of the Gadidae and it will be found that the pattern varies in a definite manner according to the methods of feeding, and the character of the food. In carrying out this research we are very much indebted to the exhaustive examination of the stomach contents by Cunningham (1896) and more recently by Borley and Thursby-Pelham (1926). Before describing the medulla oblongata in the various members of the Cod family, it is necessary to point out the marked difference in the naked eye appearance of the hind-brains of the Cyprinidae and Gadidae. In Cyprinidae the brain is characterized by the great development of the vagal and facial lobes. The vagal lobes form a pair of large swellings on either side of the rhomboid fossa and embrace between their anterior ends the unpaired facial lobe—a rounded body situated in mid line behind the cerebellum. This “lobus impar” represents apparently “a fusion of the two small facial lobes seen in the Cod” (Goronowitsch, 1897). The dorsal surface of the medulla in the Cod is occupied by a series of swellings that almost entirely close the rhomboid fossa.

scholarly journals Histomorphometric and immunohistochemical evaluation of the frontal cerebral cortex in diabetic rats after treatment with melatonin

2020 ◽  
Vol 40 (12) ◽  
pp. 1077-1087
Author(s):  
Marina G.P. Baptista ◽  
Cintia G.M. Ferreira ◽  
Yuri M.L. Albuquerque ◽  
Carolline G. D’assunção ◽  
Rebeca C. Alves ◽  
...  
Keyword(s):  
Cerebral Cortex ◽  
Frontal Cortex ◽  
Intraperitoneal Administration ◽  
Diabetic Rats ◽  
Hypoglycemic Agents ◽  
Albino Rats ◽  
Tnf Α ◽  
Frontal Cerebral Cortex ◽  
The Impact ◽  
The Brain

ABSTRACT: The central nervous system is vulnerable to complications caused by diabetes. These complications lead to increased oxidative stress in the brain, resulting in damage to the cerebral cortex, among other regions. Insulin and hypoglycemic agents are still the most widely used treatments. However, current research with an experimental model of diabetes suggests the use of antioxidants, such as melatonin. Thus, we tested the hypothesis that exogenous melatonin may decrease or prevent the effects of diabetes in the frontal cortex of the rat brain. Fifty albino rats were allocated into five groups: GC = rats without diabetes induction, GD = diabetic rats induced by streptozotocin, GDM = streptozotocin-induced and melatonin-treated diabetic rats, GDI = diabetic rats induced by streptozotocin and treated with insulin, GDMI = diabetic rats induced by streptozotocin and treated with melatonin and insulin simultaneously. Diabetes was induced by intraperitoneal administration of streptozotocin (60mg/kg). Insulin (5U/day) was administered subcutaneously and melatonin (10mg/kg) by drinking water; both treatments last days after. We analyzed animals’ weight, the cytokines IL-6 and TNF-α, apoptosis, glycogen, and did morphometry and histopathology of the frontal cortex were analyzed. The results showed that the cerebral cortex of the diabetic animals presented axonal degeneration, reduced number of neurons in the cortex, reduced glycogen, increased IL-6 and TNF-α expression, high apoptotic index, and reduced animal weight and the brain. Treatment with melatonin associated or not with insulin prevented such effects. Thus, we conclude that melatonin associated with insulin may be an alternative for avoiding the impact of diabetes in the brain’s frontal cortex.

Do Rats Have Prefrontal Cortex? The Rose-Woolsey-Akert Program Reconsidered

1995 ◽  
Vol 7 (1) ◽  
pp. 1-24 ◽  
Author(s):  
Todd M. Preuss
Keyword(s):  
Prefrontal Cortex ◽  
Frontal Cortex ◽  
Frontal Lobe ◽  
Dorsolateral Prefrontal Cortex ◽  
Delayed Reaction ◽  
Frontal Lobe Function ◽  
Mediodorsal Thalamic Nucleus ◽  
Dorsolateral Prefrontal ◽  
Prefrontal Region ◽  
Higher Cognitive Functions

Primates are unique among mammals in possessing a region of dorsolateral prefrontal cortex with a well-developed internal granular layer. This region is commonly implicated in higher cognitive functions. Despite the histological distinctiveness of primate dorsolateral prefrontal cortex, the work of Rose, Woolsey, and Akert produced a broad consensus among neuroscientists that homologues of primate granular frontal cortex exist in nonprimates and can be recognized by their dense innervation from the mediodorsal thalamic nucleus (MD). Additional characteristics have come to be identified with dorsolateral prefrontal cortex, including rich dopaminergic innervation and involvement in spatial delayed-reaction tasks. However, recent studies reveal that these characteristics are not distinctive of the dorsolateral prefrontal region in primates: MD and dopaminergic projections are widespread in the frontal lobe, and medial and orbital frontal areas may play a role in delay tasks. A reevaluation of rat frontal cortex suggests that the medial frontal cortex, usually considered to be homologous to the dorsolateral prefrontal cortex of primates, actually consists of cortex homologous to primate premotor and anterior cin-date cortex. The lateral MD-projection cortex of rats resembles portions of primate orbital cortex. If prefrontal cortex is construed broadly enough to include orbital and cingulate cortex, rats can be said to have prefrontal cortex. However, they evidently lack homologues of the dorsolateral prefrontal areas of primates. This assessment suggests that rats probably do not provide useful models of human dorsolateral frontal lobe function and dysfunction, although they might prove valuable for understanding other regions of frontal cortex.

scholarly journals The volume of the anatomical connections of the frontal lobes

2020 ◽  
Vol V (4) ◽  
pp. 1-15
Author(s):  
M. N. Zhukovsky
Keyword(s):  
Cerebral Cortex ◽  
Frontal Lobe ◽  
Frontal Lobes ◽  
Controversial Issues ◽  
Subsequent Processing ◽  
The Brain ◽  
Anatomical Part

The question of the connection between the frontal lobes and the various parts of the brain still remains far from solved completely, despite a whole series of studies in this direction. In view of this, at the suggestion of the highly respected teacher V.M.Bekhterev, I undertook this work with the aim of clarifying this issue in detail. My study consisted in the destruction of the frontal lobes in animals with the subsequent processing of their brains according to the Marchi method, and in addition, in a detailed study of physiological phenomena in the operated animals. But regarding the second part of my work, I intend to speak in another section, limiting myself at the present to the anatomical part. Before proceeding to the presentation of the results obtained by me, I will try to briefly outline the literature of the question of interest to me. The literature on the connections of the frontal lobe with various areas of the brain is directly adjacent to the literature on the connections of the cerebral cortex in general and seems to be very extensive, which is why I will confine myself to a more detailed sketch of a part of it, concerning more or less controversial issues, mentioning only briefly about the research on which there is a contradiction.

Oligodendrocytes in Developing Hameter Cerebral Cortex

1976 ◽  
Vol 34 ◽  
pp. 126-127
Author(s):  
MB. Tank Buschmann
Keyword(s):  
Cerebral Cortex ◽  
Optic Nerve ◽  
Frontal Cortex ◽  
Osmium Tetroxide ◽  
Sodium Cacodylate Buffer ◽  
Sodium Cacodylate ◽  
Tissue Samples ◽  
Cacodylate Buffer ◽  
Layer V ◽  
Adult Hamster

Development of oligodendrocytes in rat corpus callosum was described as a sequential change in cytoplasmic density which progressed from light to medium to dark (1). In rat optic nerve, changes in cytoplasmic density were not observed, but significant changes in morphology occurred just prior to and during myelination (2). In our study, the ultrastructural development of oligodendrocytes was studied in newborn, 5-, 10-, 15-, 20-day and adult frontal cortex of the golden hamster (Mesocricetus auratus).Young and adult hamster brains were perfused with paraformaldehyde-glutaraldehyde in sodium cacodylate buffer at pH 7.3 according to the method of Peters (3). Tissue samples of layer V of the frontal cortex were post-fixed in 2% osmium tetroxide, dehydrated in acetone and embedded in Epon-Araldite resin.

Glucuronyl 3-sulfate occurs exclusively on distal unmyelinated terminals of selected sensory neurons in the peripheral nervous system

1995 ◽  
Vol 53 ◽  
pp. 958-959
Author(s):  
S.S. Spicer ◽  
B.A. Schulte
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Cerebral Cortex ◽  
Peripheral Nervous System ◽  
Sensory Neurons ◽  
Sensory Nerves ◽  
Tissue Antigens ◽  
The Central Nervous System ◽  
The Brain ◽  
Leu 7

Generation of monoclonal antibodies (MAbs) against tissue antigens has yielded several (VC1.1, HNK- 1, L2, 4F4 and anti-leu 7) which recognize the unique sugar epitope, glucuronyl 3-sulfate (Glc A3- SO4). In the central nervous system, these MAbs have demonstrated Glc A3-SO4 at the surface of neurons in the cerebral cortex, the cerebellum, the retina and other widespread regions of the brain.Here we describe the distribution of Glc A3-SO4 in the peripheral nervous system as determined by immunostaining with a MAb (VC 1.1) developed against antigen in the cat visual cortex. Outside the central nervous system, immunoreactivity was observed only in peripheral terminals of selected sensory nerves conducting transduction signals for touch, hearing, balance and taste. On the glassy membrane of the sinus hair in murine nasal skin, just deep to the ringwurt, VC 1.1 delineated an intensely stained, plaque-like area (Fig. 1). This previously unrecognized structure of the nasal vibrissae presumably serves as a tactile end organ and to our knowledge is not demonstrable by means other than its selective immunopositivity with VC1.1 and its appearance as a densely fibrillar area in H&E stained sections.

Neurotransmitter systems of female mouse brain during growth of malignant melanoma modeled on the background of chronic pain

2018 ◽  
pp. 49-55
Author(s):  
О.И. Кит ◽  
И.М. Котиева ◽  
Е.М. Франциянц ◽  
И.В. Каплиева ◽  
Л.К. Трепитаки ◽  
...  
Keyword(s):  
Chronic Pain ◽  
Cerebral Cortex ◽  
Malignant Melanoma ◽  
Sciatic Nerve ◽  
Female Mouse ◽  
Combined Effects ◽  
Malignant Growth ◽  
Course Of Disease ◽  
The Brain ◽  
Melanoma Growth

Известно, что биогенные амины (БА) участвуют в злокачественном росте, их уровень изменяется в ЦНС при болевом воздействии, однако исследований о сочетанном влиянии хронической боли (ХБ) и онкопатологии на динамику БА в головном мозге не проводилось. Цель: изучить особенности баланса БА в коре головного мозга в динамике роста меланомы, воспроизведенной на фоне ХБ. Материалы и методы. Работа выполнена на 64 мышах-самках, весом 21-22 г. Животным основной группы меланому В16/F10 перевивали под кожу спины через 2 недели после перевязки седалищных нервов. Группой сравнения служили мыши с меланомой без боли. Уровни БА: адреналина, норадреналина, дофамина (ДА), серотонина (5-НТ), гистамина, а также 5-ОИУК определяли методом иммуноферментного анализа. Результаты. У мышей с ХБ уменьшается содержание большинства БА, однако уровень ДА не изменяется. Метаболизм 5-НТ происходит с участием МАО. Развитие меланомы сопровождается увеличением содержания ДА и 5-НТ, тогда как МАО - ингибируется. Направленность сдвигов БА при развитии меланомы на фоне ХБ оказалась практически такой же, как и без неё. В то же время ХБ ограничивает накопление 5-НТ в коре мозга при меланоме, что сопровождается более агрессивным её течением. Выводы. ХБ ограничивает включение стресс-лимитирующих механизмов в головном мозге при развитии меланомы у мышей, что приводит к более агрессивному течению злокачественного процесса. Biogenic amines (BA) are known to be involved in malignant growth, and their CNS levels change in pain; however, there are no studies of combined effects of chronic pain (CP) and cancer on BA dynamics in the brain. Aim: To study features of BA balance in the cerebral cortex during melanoma growth associated with CP. Material and methods. The study included 64 female mice weighing 21-22 g. In the main groups, B16/F10 melanoma was transplanted under the skin of the back two weeks following sciatic nerve ligation. Mice with melanoma without pain were used as the control. Concentrations of BA: adrenaline, noradrenaline, dopamine (DA), serotonin (5-HT), histamine and 5-HIAA were measured with ELISA. Results. Concentrations of BAs decreased in mice with CP although DA levels did not change. 5-HT metabolism involved MAO. The development of melanoma was accompanied by increases in DA and 5-HT whereas MAO was inhibited. The direction of BA changes during the development of melanoma was the same with and without CP. At the same time, CP with melanoma limited accumulation of 5-HT in the cerebral cortex, which resulted in even more aggressive course of cancer. Conclusion. CP restricted the activation of cerebral stress-limiting mechanisms during the development of melanoma in mice, which resulted in a more aggressive course of disease.

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