The footprints of neuroscience in Alexandria during the 3rd-century BC: Herophilus and Erasistratus

2018 ◽  
Vol 28 (4) ◽  
pp. 186-194
Author(s):  
Maria Ioanna Stefanou
Keyword(s):  
Neurological Disease ◽  
Cranial Nerves ◽  
Sensory Nerves ◽  
Hellenistic Period ◽  
Physiological Properties ◽  
Brain Sciences ◽  
History Of ◽  
Human Dissection ◽  
Human Intellect ◽  
The Brain

In the first half of the 3rd-century BC in Alexandria, the Greek physicians Herophilus of Chalcedon (ca. 330 to ca. 260 BC) and Erasistratus of Chios (ca. 315 to ca. 240 BC) became the first scientists in antiquity to comprehensively study the anatomical underpinnings and the physiological properties of mind processes. Their scientific theories were based on experimental evidence arising from anatomical human dissection studies. Among their neuroscientific achievements were the discovery of the cranial nerves, the meninges, the dural sinuses and the ventricles; the delineation of the motor and sensory nerves; the appraisal of the brain as the seat of consciousness and human intellect; and the attribution of neurological disease to dysfunction of the nervous system. This paper will discuss the short-lived historical circumstances that enabled the ground-breaking progress in the domain of brain sciences during the Hellenistic period. In addition, this paper will examine the intriguing social, political and cultural interplays that determined the resonance of Herophilus and Erasistratus’s work and influenced the course of history of neuroscience.

scholarly journals VIII—On Diencephalic and Mesencephalic Nuclei and fibre paths in the brains of three deep sea fish

1935 ◽  
Vol 224 (516) ◽  
pp. 361-419 ◽  
Keyword(s):  
Natural History ◽  
Deep Sea ◽  
Cranial Nerves ◽  
Personal Communication ◽  
The Bahamas ◽  
History Of ◽  
The Brain ◽  
Sea Fish ◽  
External Form

Although a number of excellent papers have appeared on the brains of teleosts in general, very few studies have been reported on the brains of deep sea fish. A paper by Trojan (1906) gives but a superficial survey, while that by Gierse (1904) deals primarily with the external form of the brain, the accessory organs of the brain, and the peripheral cranial nerves. The purpose of this investigation is to present a somewhat detailed description of the cell areas and fibre pathways, especially of the diencephalon and mesencephalon, the object being to determine what modifications have taken place in connection with their unusual environment. Very little is known about the natural history of these fish. In a personal communication concerning them, Professor Burr says, “The Diaphus dumerili were collected by the Bingham Oceanographic Expedition off the Cat Islands, the Bahamas, in 1927. Of these there are six specimens, Bingham Collection Nos. 9, 21, 36, 37, 38, and 39. The two Saurida suspicio , Bingham Collection Nos. 19 and 40, were collected also off Gat Island, the Bahamas. The Bathypterois articolar phenox is a very rare specimen; it was collected at N. 20°— 16' W. 71°— 18', at a depth of from 900—945 fathoms, also in 1927.”

The birth of the neuromolecular gaze

2010 ◽  
Vol 23 (1) ◽  
pp. 11-36 ◽  
Author(s):  
Joelle M. Abi-Rached ◽  
Nikolas Rose
Keyword(s):  
Intellectual Development ◽  
Social Role ◽  
Historical Context ◽  
Institution Building ◽  
New Thought ◽  
Brain Sciences ◽  
History Of ◽  
The 1960S ◽  
Object Of Study ◽  
The Brain

The aim of this article is (1) to investigate the ‘neurosciences’ as an object of study for historical and genealogical approaches and (2) to characterize what we identify as a particular ‘style of thought’ that consolidated with the birth of this new thought community and that we term the ‘neuromolecular gaze’. This article argues that while there is a long history of research on the brain, the neurosciences formed in the 1960s, in a socio-historical context characterized by political change, faith in scientific and technological progress, and the rise of a molecular gaze in the life sciences. They flourished in part because these epistemological and technological developments were accompanied by multiple projects of institution-building. An array of stakeholders was mobilized around the belief that breakthroughs in understanding the brain were not only crucial, they were possible by means of collaborative efforts, cross-disciplinary approaches and the use of a predominantly reductionist neuromolecular method. The first part of the article considers some of the different approaches that have been adopted to writing the history of the brain sciences. After a brief outline of our own approach, the second part of the article uses this in a preliminary exploration of the birth of the neurosciences in three contexts. We conclude by arguing that the 1960s constitute an important ‘break’ in the long path of the history of the brain sciences that needs further analysis. We believe this epistemological shift we term the ‘neuromolecular gaze’ will shape the future intellectual development and social role of the neurosciences.

scholarly journals VII.—On the Physiological Action of Light

1873 ◽  
Vol 27 (1) ◽  
pp. 141-166 ◽  
Author(s):  
James Dewar ◽  
John Gray
Keyword(s):  
Optic Nerve ◽  
Sense Organ ◽  
Sensory Nerves ◽  
Histological Structure ◽  
Du Bois ◽  
Terminal Organ ◽  
Physiological Properties ◽  
Continuous Current ◽  
Electrical Stimuli ◽  
The Brain

Sensory nerves are divided into two classes, those of general sensibility and those of special sense. The nerves of general sensibility are distributed to the skin, muscles, or viscera, and convey influences to the brain which give rise to sensations of touch, heat, &c., or to those vague sensations, not definitely localised, which we include under the name of the muscular sense. The nerves of special sense are endowed with special and individual physiological properties. When a nerve of this order is irritated in any way, either by mechanical, chemical, or electrical stimuli, an influence is conveyed to the brain which gives rise to the same kind of sensation as that produced by the normal stimulus on the terminal organ. For example, pressure on the eyeball, as shown by Newton and Young, electrical stimulation by a continuous current, as demonstrated by Pfaff, Helmholtz Ritter, Purkinje, Du Bois-Reymond, and Schelske, produce many of the phenomena of vision, including not only the perception of light, but the perception of various colours and tints. But while this is the case, it is equally certain that each terminal organ responds to its normal stimulus. Thus the retina, though capable of stimulation by pressure or electricity, is specially fitted by its histological structure for the reception of those minute vibrations of the ether which constitute light. But while the terminal organ is capable of receiving a most delicate action of the normal stimulus, the nerve in connection with it is not so affected. For example, although the retina is affected by light, the optic nerve is not so, as may be proved by Marriotte's well-known experiment, by which it may be demonstrated that when the image of an external object falls on the entrance of the optic nerve, there is no corresponding sensation. The nerve is thus insensible to the normal stimulus of the sense organ, the retina.

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.

Philosophy and the Brain Sciences: Confrontation or Merger?

1980 ◽  
Vol 25 (12) ◽  
pp. 1008-1009
Author(s):  
DAVID L. WILSON
Keyword(s):  
Brain Sciences ◽  
The Brain

scholarly journals L2HGDH Missense Variant in a Cat with L-2-Hydroxyglutaric Aciduria

Genes ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 682
Author(s):  
Matthias Christen ◽  
Nils Janzen ◽  
Anne Fraser ◽  
Adrian C. Sewell ◽  
Vidhya Jagannathan ◽  
...  
Keyword(s):  
Current Knowledge ◽  
Genetic Defect ◽  
Clinical Signs ◽  
Missense Variant ◽  
Microcytic Anemia ◽  
Abnormal Behavior ◽  
Functional Candidate Gene ◽  
History Of ◽  
The Brain ◽  
Hydroxyglutaric Acid

A 7-month-old, spayed female, domestic longhair cat with L-2-hydroxyglutaric aciduria (L-2-HGA) was investigated. The aim of this study was to investigate the clinical signs, metabolic changes and underlying genetic defect. The owner of the cat reported a 4-month history of multiple paroxysmal seizure-like episodes, characterized by running around the house, often in circles, with abnormal behavior, bumping into obstacles, salivating and often urinating. The episodes were followed by a period of disorientation and inappetence. Neurological examination revealed an absent bilateral menace response. Routine blood work revealed mild microcytic anemia but biochemistry, ammonia, lactate and pre- and post-prandial bile acids were unremarkable. MRI of the brain identified multifocal, bilaterally symmetrical and T2-weighted hyperintensities within the prosencephalon, mesencephalon and metencephalon, primarily affecting the grey matter. Urinary organic acids identified highly increased levels of L-2-hydroxyglutaric acid. The cat was treated with the anticonvulsants levetiracetam and phenobarbitone and has been seizure-free for 16 months. We sequenced the genome of the affected cat and compared the data to 48 control genomes. L2HGDH, coding for L-2-hydroxyglutarate dehydrogenase, was investigated as the top functional candidate gene. This search revealed a single private protein-changing variant in the affected cat. The identified homozygous variant, XM_023255678.1:c.1301A>G, is predicted to result in an amino acid change in the L2HGDH protein, XP_023111446.1:p.His434Arg. The available clinical and biochemical data together with current knowledge about L2HGDH variants and their functional impact in humans and dogs allow us to classify the p.His434Arg variant as a causative variant for the observed neurological signs in this cat.

scholarly journals Molecular evolutionary analysis of human primary microcephaly genes

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Nashaiman Pervaiz ◽  
Hongen Kang ◽  
Yiming Bao ◽  
Amir Ali Abbasi
Keyword(s):  
Evolutionary History ◽  
Genetic Basis ◽  
Brain Size ◽  
Primate Species ◽  
Evolutionary Analysis ◽  
Australopithecus Afarensis ◽  
Primary Microcephaly ◽  
Modern Humans ◽  
History Of ◽  
The Brain

Abstract Background There has been a rapid increase in the brain size relative to body size during mammalian evolutionary history. In particular, the enlarged and globular brain is the most distinctive anatomical feature of modern humans that set us apart from other extinct and extant primate species. Genetic basis of large brain size in modern humans has largely remained enigmatic. Genes associated with the pathological reduction of brain size (primary microcephaly-MCPH) have the characteristics and functions to be considered ideal candidates to unravel the genetic basis of evolutionary enlargement of human brain size. For instance, the brain size of microcephaly patients is similar to the brain size of Pan troglodyte and the very early hominids like the Sahelanthropus tchadensis and Australopithecus afarensis. Results The present study investigates the molecular evolutionary history of subset of autosomal recessive primary microcephaly (MCPH) genes; CEP135, ZNF335, PHC1, SASS6, CDK6, MFSD2A, CIT, and KIF14 across 48 mammalian species. Codon based substitutions site analysis indicated that ZNF335, SASS6, CIT, and KIF14 have experienced positive selection in eutherian evolutionary history. Estimation of divergent selection pressure revealed that almost all of the MCPH genes analyzed in the present study have maintained their functions throughout the history of placental mammals. Contrary to our expectations, human-specific adoptive evolution was not detected for any of the MCPH genes analyzed in the present study. Conclusion Based on these data it can be inferred that protein-coding sequence of MCPH genes might not be the sole determinant of increase in relative brain size during primate evolutionary history.

scholarly journals Human Monocytes Plasticity in Neurodegeneration

Biomedicines ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 717
Author(s):  
Ilenia Savinetti ◽  
Angela Papagna ◽  
Maria Foti
Keyword(s):  
Neurodegenerative Disorders ◽  
Current Knowledge ◽  
Neurological Diseases ◽  
Surface Marker ◽  
First Line ◽  
Surface Marker Expression ◽  
Physiological Properties ◽  
Attractive Therapeutic Target ◽  
The Brain ◽  
Lateral Sclerosis

Monocytes play a crucial role in immunity and tissue homeostasis. They constitute the first line of defense during the inflammatory process, playing a role in the pathogenesis and progression of diseases, making them an attractive therapeutic target. They are heterogeneous in morphology and surface marker expression, which suggest different molecular and physiological properties. Recent evidences have demonstrated their ability to enter the brain, and, as a consequence, their hypothetical role in different neurodegenerative diseases. In this review, we will discuss the current knowledge about the correlation between monocyte dysregulation in the brain and/or in the periphery and neurological diseases in humans. Here we will focus on the most common neurodegenerative disorders, such as Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis and multiple sclerosis.

Streptococcus pluranimalium meningoencephalitis in a horse

2021 ◽  
pp. 104063872110234
Author(s):  
Dah-Jiun Fu ◽  
Akhilesh Ramachandran ◽  
Craig Miller
Keyword(s):  
Ribosomal Rna ◽  
Cross Sections ◽  
Nucleotide Sequencing ◽  
Formalin Fixed Paraffin ◽  
Quarter Horse ◽  
Formalin Fixed Paraffin Embedded ◽  
History Of ◽  
The Brain ◽  
Gram Positive Cocci ◽  
Formalin Fixed

A 3-y-old, female Quarter Horse with a history of acute neurologic signs was found dead and was submitted for postmortem examination. Areas of petechial and ecchymotic hemorrhage were present on cross-sections of the cerebrum, cerebellum, and brainstem. Histologic examination of the brain revealed severe, purulent meningoencephalitis and vasculitis with a myriad of intralesional gram-positive cocci. Streptococcus pluranimalium was identified from formalin-fixed, paraffin-embedded tissue obtained from sites with active lesions by PCR and nucleotide sequencing of bacterial 16S ribosomal RNA. S. pluranimalium should be considered as a cause of meningoencephalitis in a horse.

scholarly journals A Rare Case of Spontaneous Arachnoid Cyst Rupture Presenting as Right Hemiplegia and Expressive Aphasia in a Pediatric Patient

Children ◽  
2021 ◽  
Vol 8 (2) ◽  
pp. 78
Author(s):  
Anne Bryden ◽  
Natalie Majors ◽  
Vinay Puri ◽  
Thomas Moriarty
Keyword(s):  
Cognitive Processing ◽  
Arachnoid Cyst ◽  
Memory Loss ◽  
Acute Onset ◽  
Word Finding ◽  
Outpatient Visits ◽  
The Family ◽  
History Of ◽  
Cyst Rupture ◽  
The Brain

This study examines an 11-year-old boy with a known history of a large previously asymptomatic arachnoid cyst (AC) presenting with acute onset of right facial droop, hemiplegia, and expressive aphasia. Shortly after arrival to the emergency department, the patient exhibited complete resolution of right-sided hemiplegia but developed headache and had persistent word-finding difficulties. Prior to symptom onset while in class at school, there was an absence of reported jerking movements, headache, photophobia, fever, or trauma. At the time of neurology consultation, the physical exam showed mildly delayed cognitive processing but was otherwise unremarkable. The patient underwent MRI scanning of the brain, which revealed left convexity subdural hematohygroma and perirolandic cortex edema resulting from ruptured left frontoparietal AC. He was evaluated by neurosurgery and managed expectantly. He recovered uneventfully and was discharged two days after presentation remaining asymptomatic on subsequent outpatient visits. The family express concerns regarding increased anxiety and mild memory loss since hospitalization.

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