Some Observations on the Cytological Effects of Antimitotic Poisons

1968 ◽  
Vol 17 (1) ◽  
pp. 182-184
Author(s):  
Pierre Dustin

Recently discovered substances with antimitotic action fall in the two categories which have been defined since many years, i. e. spindle poisons and chromatin (or “radiomimetic”) poisons. The most recently studied are hydroxyurea — a powerful inhibitor of DNA synthesis — and the Vinca alcaloids — which destroy the tubular components of the spindle, bringing a prolonged arrest in metaphase.The mechanisms of action of many of these drugs remain most obscure. In the field of spindle-poisons, there has been no explanation sofar of the relationship between their chemical structure and cytological action. While it is known that minor changes in the chemical structure of colchicine can prevent its specific action on the spindle, the precise relation which appears to exist between this complex molecule and the spindle structures remains obscure. The same remark applies to the Vinca alcaloids. Progress is being made however in this field. The ultrastructural aspects of the spindle have been analysed by electron microscopy, and a precise definition in chemical terms of the spindle may be close. These observations have shown the similarity between the tubules of the spindle and other tubular structures of identifical size: the neurotubules. Some recent observations indicate that these may also be destroyed by colchicine, a fact which may be related to the well-known and severe neurotoxicity of this alcaloid. What remains to be explained is the fact that the most effective spindle poisons are molecules of the size and complexity of those of vinblastine, while simple inorganic substances (arsenicals, heavy metals) may exert identical if not so powerful effects on the spindle structures. Another point which needs further research is the cause of the extensive cellular destruction which follows, in animal cells, any prolonged inhibition of the spindle function. The chemotherapic actions of spindle poisons are most probably related, not only to the growth inhibiting effects of these drugs, but most of all to the cellular breakdown which is observed in cells when they have been kept for several hours in metaphase.

2019 ◽  
Vol 70 (3) ◽  
pp. 843-847 ◽  
Author(s):  
Oana Roxana Ciobotaru ◽  
Mary-Nicoleta Lupu ◽  
Laura Rebegea ◽  
Octavian Catalin Ciobotaru ◽  
Oana Monica Duca ◽  
...  

Dexamethasone is a synthetic glucocorticoid used for its anti-inflammatory and analgesic effect. In addition to these therapeutic indications, it is also recommended for nausea and vomiting treatment which may occur during the postoperative period, with impact on postoperative evolution, regarding the evolution of wound healing and length of stay (LOS), with a reflection on the costs of hospital admission. Therefore, their prevention is very important for both patients� comfort and a good recovery.


2019 ◽  
Vol 77 (9) ◽  
Author(s):  
Narges Dastmalchi ◽  
Seyed Mahdi Banan Khojasteh ◽  
Mirsaed Miri Nargesi ◽  
Reza Safaralizadeh

ABSTRACT Helicobacter pylori infection performs a key role in gastric tumorigenesis. Long non-coding RNAs (lncRNAs) have demonstrated a great potential to be regarded as effective malignancy biomarkers for various gastrointestinal diseases including gastric cancer (GC). The present review highlights the relationship between lncRNAs and H. pylori in GC. Several studies have examined not only the involvement of lncRNAs in H. pylori-associated GC progression but also their molecular mechanisms of action. Among the pertinent studies, some have addressed the effects of H. pylori infection on modulatory networks of lncRNAs, while others have evaluated the effects of changes in the expression level of lncRNAs in H. pylori-associated gastric diseases, especially GC. The relationship between lncRNAs and H. pylori was found to be modulated by various molecular pathways.


2021 ◽  
Vol 22 (8) ◽  
pp. 4203
Author(s):  
Giorgio Valabrega ◽  
Giulia Scotto ◽  
Valentina Tuninetti ◽  
Arianna Pani ◽  
Francesco Scaglione

Poly(ADP-ribose) polymerases (PARP) are proteins responsible for DNA damage detection and signal transduction. PARP inhibitors (PARPi) are able to interact with the binding site for PARP cofactor (NAD+) and trapping PARP on the DNA. In this way, they inhibit single-strand DNA damage repair. These drugs have been approved in recent years for the treatment of ovarian cancer. Although they share some similarities, from the point of view of the chemical structure and pharmacodynamic, pharmacokinetic properties, these drugs also have some substantial differences. These differences may underlie the different safety profiles and activity of PARPi.


1982 ◽  
Vol 1 (1) ◽  
pp. 24-27 ◽  
Author(s):  
I. Taitl

Fired resistors exhibit variations which are minimised by abrasive and laser trimming. The latter may cause unstable behaviour which is further aggravated by thermal shock. The chemical structure of a thick film resistor is analysed with respect to mechanical stress, and the theoretical conclusion that the coefficient of thermal expansion of the resistor should be equal to or smaller than that of the substrate is verified experimentally. The thermal behaviour of ruthenium dioxide is examined and a range of CTE values are determined for materials of varying chemical composition. The relationship between CTE and post laser trimming stability is demonstrated on four thick film resistors which differ in thermal expansion. It is pointed out that formulations with high metallic content can absorb tensile stress by elastic deformation, thus minimising the formation or propagation of laser induced cracks.


1968 ◽  
Vol 17 (7) ◽  
pp. 1385-1399 ◽  
Author(s):  
D.W. Schneck ◽  
W.J. Racz ◽  
G.H. Hirsch ◽  
G.L. Bubbar ◽  
G.S. Marks

Sign in / Sign up

Export Citation Format

Share Document