HISTOMORPHOLOGICAL CHANGES IN THE BRAIN IN RELATION TO OVARIAN CYCLE OF FRESHWATER CRAB, BARYTELPHUSA CUNICULARIS

2017 ◽  
Vol 23 (1) ◽  
Author(s):  
C.A. JAWALE
Keyword(s):  
Staining Intensity ◽  
Neurosecretory Cells ◽  
Ovarian Cycle ◽  
Secretory Product ◽  
Freshwater Crab ◽  
Intensity Index ◽  
Cytoplasmic Material ◽  
Histomorphological Changes ◽  
Cyclic Changes ◽  
The Brain

Ovarian maturation by neurosecretory cells in the brain of freshwater crab, Barytelphusa cunicularis have been examined. The histological scrutiny of the brain of Barytelphusa cunicularis related with three types (A, B and C) of neurosecretory cells, which are classified on the basis of size, shape and tinctorial characters. All these types of cells marked annual cyclic changes of cytoplasmic material in association with ovarian cycle. The activity of these cells has been correlated with the ovarian cycle. They are distinguishable by their size, nature locations, shape, nucleus position, cell measure and the secretory product in the cytoplasm. The result indicates that the neurosecretory A, B and C cells of the brain seen involved in the process of mating ovulation. The neurosecretory materials staining intensity index of these cells is described.

Age-related histological changes in neurosecretory cells in the supraoesophageal ganglion of Nereis virens (Annelida, Polychaeta)

1980 ◽  
Vol 58 (10) ◽  
pp. 1735-1740 ◽  
Author(s):  
Kathryn Bell ◽  
Joan R. Marsden
Keyword(s):  
Light Microscopy ◽  
Developmental Stages ◽  
Cell Types ◽  
Staining Intensity ◽  
Neurosecretory Cells ◽  
Histological Changes ◽  
Nereis Virens ◽  
Age Related ◽  
P Cells ◽  
The Brain

The supraoesophageal ganglion of Nereis virens has been surveyed by light microscopy to determine the locations of probable neurosecretory cells. Neurons reacting with paraldehyde fuchsin are found scattered throughout the brain, but the majority are accumulated posteriorly in nucleus 20. This nucleus was examined in some detail, and the histology of four cell types is described. Two types (p and r) are strongly paraldehyde-fuchsin-positive, and may be secretory. On the basis of other staining characteristics, and uptake of labelled cystine, it is concluded that p cells are rich in cystine and (or) cysteine. A comparison of juvenile and adult brains revealed that the same cell types exist at both developmental stages, but that p and r cells increase in number and staining intensity with age. These findings are not consistent with the notion that these particular cells are the source of a "juvenile hormone' ' which has been reported to exist in nereids. Rather it is suggested that the described cells are producers of a maturation and (or) spawning hormone.

The brain structure and neurosecretory cells of noctuid moth Anadevidia peponis: Noctuidae

1990 ◽  
Vol 48 (3) ◽  
pp. 436-437
Author(s):  
M. Sato ◽  
Y. Ogawa ◽  
M. Sasaki ◽  
T. Matsuo
Keyword(s):  
Biological Clock ◽  
Virgin Female ◽  
Basic Structure ◽  
Fixed Time ◽  
Neurosecretory Cells ◽  
Nerve Cells ◽  
Noctuid Moth ◽  
The Right ◽  
20 Nm ◽  
The Brain

A virgin female of the noctuid moth, a kind of noctuidae that eats cucumis, etc. performs calling at a fixed time of each day, depending on the length of a day. The photoreceptors that induce this calling are located around the neurosecretory cells (NSC) in the central portion of the protocerebrum. Besides, it is considered that the female’s biological clock is located also in the cerebral lobe. In order to elucidate the calling and the function of the biological clock, it is necessary to clarify the basic structure of the brain. The observation results of 12 or 30 day-old noctuid moths showed that their brains are basically composed of an outer and an inner portion-neural lamella (about 2.5 μm) of collagen fibril and perineurium cells. Furthermore, nerve cells surround the cerebral lobes, in which NSCs, mushroom bodies, and central nerve cells, etc. are observed. The NSCs are large-sized (20 to 30 μm dia.) cells, which are located in the pons intercerebralis of the head section and at the rear of the mushroom body (two each on the right and left). Furthermore, the cells were classified into two types: one having many free ribosoms 15 to 20 nm in dia. and the other having granules 150 to 350 nm in dia. (Fig. 1).

Neurosecretory Cells in the Brain of the Larva of Lucilia caesar L.

Nature ◽  
1957 ◽  
Vol 179 (4553) ◽  
pp. 257-258 ◽  
Author(s):  
ALASTAIR FRASER
Keyword(s):  
Neurosecretory Cells ◽  
The Brain

Neural glymphatic system: Clinical implications and potential importance of melatonin

2021 ◽  
Vol 4 (4) ◽  
pp. 551-565
Author(s):  
Ryan D Bitar ◽  
Jorge L Torres-Garza ◽  
Russel J Reiter ◽  
William T Phillips
Keyword(s):  
Lymph Nodes ◽  
Subarachnoid Space ◽  
Slow Wave Sleep ◽  
Lymphatic Vessels ◽  
Amyloid Β ◽  
Secretory Product ◽  
Cervical Lymph Nodes ◽  
Waste Products ◽  
Glymphatic System ◽  
The Brain

The central nervous system was thought to lack a lymphatic drainage until the recent discovery of the neural glymphatic system.  This highly specialized waste disposal network includes classical lymphatic vessels in the dura that absorb fluid and metabolic by-products and debris from the underlying cerebrospinal fluid (CSF) in the subarachnoid space. The subarachnoid space is continuous with the Virchow-Robin peri-arterial and peri-vascular spaces which surround the arteries and veins that penetrate into the neural tissue, respectively.  The dural lymphatic vessels exit the cranial vault via an anterior and a posterior route and eventually drain into the deep cervical lymph nodes. Aided by the presence of aquaporin 4 on the perivascular endfeet of astrocytes, nutrients and other molecules enter the brain from peri-arterial spaces and form interstitial fluid (ISF) that baths neurons and glia before being released into peri-venous spaces.  Melatonin, a pineal-derived secretory product which is in much higher concentration in the CSF than in the blood, is believed to follow this route and to clear waste products such as amyloid-β from the interstitial space. The clearance of amyloid-β reportedly occurs especially during slow wave sleep which happens concurrently with highest CSF levels of melatonin.  Experimentally, exogenously-administered melatonin defers amyloid-β buildup in the brain of animals and causes its accumulation in the cervical lymph nodes. Clinically, with increased age CSF melatonin levels decrease markedly, co-incident with neurodegeneration and dementia.  Collectively, these findings suggest a potential association between the loss of melatonin, decreased glymphatic drainage and neurocognitive decline in the elderly.

scholarly journals Neuropeptides in modulation of Drosophila behavior: how to get a grip on their pleiotropic actions

2019 ◽  
Author(s):  
Dick R Nässel ◽  
Dennis Pauls ◽  
Wolf Huetteroth
Keyword(s):  
Expression Pattern ◽  
Internal State ◽  
Neurosecretory Cells ◽  
Higher Order ◽  
Specific Expression ◽  
Specific Expression Pattern ◽  
Pleiotropic Functions ◽  
Pleiotropic Actions ◽  
The Brain ◽  
Different Levels

Neuropeptides constitute a large and diverse class of signaling molecules that are produced by many types of neurons, neurosecretory cells, endocrines and other cells. Many neuropeptides display pleiotropic actions either as neuromodulators, co-transmitters or circulating hormones, while some play these roles concurrently. Here, we highlight pleiotropic functions of neuropeptides and different levels of neuropeptide signaling in the brain, from context-dependent orchestrating signaling by higher order neurons, to local executive modulation in specific circuits. Additionally, orchestrating neurons receive peptidergic signals from neurons conveying organismal internal state cues and relay these to executive circuits. We exemplify these levels of signaling with four neuropeptides, SIFamide, short neuropeptide F, allatostatin-A and leucokinin, each with a specific expression pattern and level of complexity in signaling.

Neurosecretion in the Brain of the Larva of the Sheep Blowfly, Lucilia caesar

1959 ◽  
Vol s3-100 (51) ◽  
pp. 377-394
Author(s):  
ALASTAIR FRASER
Keyword(s):  
Cell Size ◽  
Neurosecretory Cells ◽  
Mature Larva ◽  
The Brain

Six groups of neurosecretory cells were identified in the brain of the mature larva of Lucilia caesar. Five of these groups belonged to the category of medial neurosecretory cells and one to that of lateral neurosecretory cells. The groups differ in position, cell size, staining characteristics, and sequence of activity. It is apparent that only some of the groups are concerned with the process of thoracic gland activation, though all function during metamorphosis. At least one group, not concerned in thoracic gland activation in the non-diapause larva, is continually active during diapause.

scholarly journals Aquaporin-4 Expression during Toxic and Autoimmune Demyelination

Cells ◽  
2020 ◽  
Vol 9 (10) ◽  
pp. 2187
Author(s):  
Sven Olaf Rohr ◽  
Theresa Greiner ◽  
Sarah Joost ◽  
Sandra Amor ◽  
Paul van der Valk ◽  
...  
Keyword(s):  
Immune Cells ◽  
Water Channel ◽  
Staining Intensity ◽  
Brain Parenchyma ◽  
Aquaporin 4 ◽  
Aqp4 Expression ◽  
Humoral Immune ◽  
Autoimmune Demyelination ◽  
Peripheral Immune Cells ◽  
The Brain

The water channel protein aquaporin-4 (AQP4) is required for a normal rate of water exchange across the blood–brain interface. Following the discovery that AQP4 is a possible autoantigen in neuromyelitis optica, the function of AQP4 in health and disease has become a research focus. While several studies have addressed the expression and function of AQP4 during inflammatory demyelination, relatively little is known about its expression during non-autoimmune-mediated myelin damage. In this study, we used the toxin-induced demyelination model cuprizone as well as a combination of metabolic and autoimmune myelin injury (i.e., Cup/EAE) to investigate AQP4 pathology. We show that during toxin-induced demyelination, diffuse AQP4 expression increases, while polarized AQP4 expression at the astrocyte endfeet decreases. The diffuse increased expression of AQP4 was verified in chronic-active multiple sclerosis lesions. Around inflammatory brain lesions, AQP4 expression dramatically decreased, especially at sites where peripheral immune cells penetrate the brain parenchyma. Humoral immune responses appear not to be involved in this process since no anti-AQP4 antibodies were detected in the serum of the experimental mice. We provide strong evidence that the diffuse increase in anti-AQP4 staining intensity is due to a metabolic injury to the brain, whereas the focal, perivascular loss of anti-AQP4 immunoreactivity is mediated by peripheral immune cells.

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