A simple fluorescent double staining method for distinguishing neuronal from non-neuronal cells in the insect central nervous system

2006 ◽  
Vol 155 (2) ◽  
pp. 202-206 ◽  
Author(s):  
Rudi Loesel ◽  
Stefan Weigel ◽  
Peter Bräunig
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Staining Method ◽  
Neuronal Cells ◽  
Double Staining ◽  
Double Staining Method ◽  
Insect Central Nervous System

Enzyme histochemical application and backscattered electron imaging to visualize the distribution of lymphatic capillaries

1990 ◽  
Vol 48 (3) ◽  
pp. 880-881
Author(s):  
Seiji Kato
Keyword(s):  
Staining Method ◽  
Double Staining ◽  
Reaction Products ◽  
Blood Capillaries ◽  
Backscattered Electron Imaging ◽  
Histochemical Observation ◽  
Backscattered Electron ◽  
Double Staining Method ◽  
Electron Imaging ◽  
Cryostat Sections

Previously, the author repeatedly confirmed the higher 5’-nucleotidase (5’-Nase) and lower alkaline phoaphatase (ALPase) activities in the wall of lymphatic capillaries reacted with the lead-based method relative to those of blood capillaries. The ALPase, on the other hand, is markedly higher in blood capillaries than in lymphatics. On the basis of these enzyme characteristics, the author has developed a 5’-Nase— ALPase double staining method to differentiate small lymphatics from blood capillaries at the level of the light microcsopy. Furthermore, we applied it to histochemical observation of the lead-containing reaction products of 5’-Nase in lymphatics on the same or adjacent cryostat sections using backscattered electron imaging (BEI) in scanning electron microscope (SEM). This paper presents a new applicability of 5’-Nase histochemistry by BEI-SEM to demonstrate the distribution of lymphatic capillaries in tissue blocks.

scholarly journals Immunohistochemical/histochemical double staining method in the study of the columnar metaplasia of the oesophagus

2014 ◽  
Vol 58 (1) ◽  
Author(s):  
D. Cabibi ◽  
A.G. Giannone ◽  
C. Mascarella ◽  
C. Guarnotta ◽  
M. Castiglia ◽  
...  
Keyword(s):  
Staining Method ◽  
Double Staining ◽  
Columnar Metaplasia ◽  
Double Staining Method

Motor responses of Rhodnius prolixus Stål (Hem., Reduviidae) to volatile drugs

1971 ◽  
Vol 61 (2) ◽  
pp. 309-313 ◽  
Author(s):  
Ian McLure
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Carbon Tetrachloride ◽  
Chloral Hydrate ◽  
Rhodnius Prolixus ◽  
The Other ◽  
Motor Responses ◽  
Normal Feeding ◽  
Insect Central Nervous System ◽  
Differential Action

Fifth-instar nymphs of Rhodnius prolixus Stålwere exposed to the vapours of 11 volatile drugs: acetone, bromobenzene, bromoform, carbon tetrachloride, chloral hydrate, chloroform, dioxane, ethanol, ethyl ether, isopropanol and paraldehyde. Bromobenzene, bromoform, carbon tetrachloride, chloroform and ether induced reversible anaesthesia. For each of these five, the insects exhibited a different andspecific pattern of motor responses before becoming totally immobile; these responses are described. The responses to carbon tetrachloride are similar to the normal feeding responses of this insect. The other six drugs did not induce anaesthesia, but instead, a commonand stereotyped pattern of cleaning responses, suggesting irritation of the sensory organs. It is proposed that the agent-specific responses to the anaesthesiainducing drugs are due to their differential action upon specific portions of the insect central nervous system.

Cell proliferation in the repairing adult insect central nervous system: incorporation of the thymidine analogue 5-bromo-2-deoxyuridine in vivo

1990 ◽  
Vol 95 (4) ◽  
pp. 599-604
Author(s):  
P.J. Smith ◽  
E.A. Howes ◽  
J.E. Treherne
Keyword(s):  
Central Nervous System ◽  
Cell Proliferation ◽  
Nervous System ◽  
Blood Brain Barrier ◽  
Glial Cells ◽  
Past Research ◽  
Thymidine Analogue ◽  
Adult Insect ◽  
Insect Central Nervous System

Uptake of the thymidine analogue 5-bromo-2-deoxyuridine into non-neuronal cells of the insect central nervous system has been examined following a controlled lesioning of the glial elements. The pattern of BUdR labelling along the penultimate abdominal connective was examined over a period of 17 days. Cell proliferation occurred in and immediately around the site of damage in both perineurial and subperineurial glial cells but at different times post-lesion for the two regions. Proliferation in the perineurial zone was maximal at 6–8 days post-lesion but continued for at least 17 days. Subperineurial proliferation was less dramatic and peaked between days 8–11 post-lesion. In both areas division appears to be confined to the reactive glial cells. These results are discussed in the context of past research on this system, particularly with regard to the restoration of the blood-brain barrier.

Adipokinetic hormone stimulates neurones in the insect central nervous system.

1995 ◽  
Vol 198 (6) ◽  
pp. 1307-1311
Author(s):  
J J Milde ◽  
R Ziegler ◽  
M Wallstein
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Manduca Sexta ◽  
Central Action ◽  
Adipokinetic Hormone ◽  
Metabolic Functions ◽  
Simple Preparation ◽  
Pressure Injection ◽  
The Central Nervous System ◽  
Insect Central Nervous System

A simple preparation designed to screen and compare the central action of putative neuroactive agents in the moth Manduca sexta is described. This approach combines microinjections into the central nervous system with myograms recorded from a pair of spontaneously active mesothoracic muscles. Pressure injection of either octopamine or Manduca adipokinetic hormone (M-AKH) into the mesothoracic neuropile increases the monitored motor activity. Under the conditions used, the excitatory effects of M-AKH exceed those of the potent neuromodulator octopamine. This suggests that M-AKH plays a role in the central nervous system in addition to its known metabolic functions and supports recent evidence that neuropeptides in insects can be multifunctional.

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