Biomedical subjects

E Pistacchio

Publications and source records attributed to E Pistacchio.

5 recordsLinked to original sources

PubMed2001

[Innovation in nineteenth century healthcare: disinfection stations].

The possibility of limiting and preventing epidemics by cleansing everything that could be touched by patients, was an intuitive thought well before microbial discoveries. In accordance with the "miasmas theory", morbid substances were emanated from the bodies of the patients. A step forward took place in the 19th century with Pasteur and Koch's discoveries and progress in chemical disinfectants. The law was slow to adapt: in Italy only in 1888 was a Code drawn up to establish some "Disinfection Stations", places for the sterilisation of infectious material from patients' homes. Later, a similar home service was started for everything that was not transportable. Thus, in the case of cholera, smallpox, scarlet fever, diphtheria, typhus, tuberculosis, etc. it became possible to sterilise everything with which patients came into contact.

History, 19th Century↗

PubMed1996

Effect of water softening and heating on microbial contamination of dental unit systems.

This study regards the quality of the water used in 4 types of dental units making use of softened and heated water, softened but non-heated water, non-softened but heated water and non-softened and non-heated water. The samples were taken from the incoming tap water, from oral rinsing cup, the air-water syringe and the ultrasound descaling hand-piece. The results showed how the water underwent a notable growth in bacteria during its passage within the circuits of the units, reaching heterotrophic total counts greatly exceeding the guidelines set down by Italian laws regarding drinking water. While the influence of softening was evident, the bacteria in the samples taken from descaling handpiece, where there is more stagnation, found excellent growing conditions also at high temperatures. In the softened and heated waters a notable growth of Pseudomonas aeruginosa was found and it is likely that this was encouraged by the combined effect of the softening and heating. As far as the origin of the contamination is concerned, the bacteria present in the water systems seem to have come from the incoming water.

Bacteria↗

PubMed1995

[Not Available].

Explore the source record for details and available documents.

Dentistry↗

PubMed1994

Effect of omega-conotoxin and verapamil on antinociceptive, behavioural and thermoregulatory responses to opioids in the rat.

This study with the rat evaluated the contribution of omega-conotoxin GVIA-(omega-CgTx) and verapamil-sensitive Ca2+ channels in behavioural, antinociceptive and thermoregulatory responses to intracerebroventricular (i.c.v.) injection of [D-Ala2,NMePhe4,Gly-ol5]enkephalin (DAMGO), [D-Pen2,D-Pen5]enkephalin (DPDPE) and dynorphin A-(1-17), which are selective agonists for putative mu, delta and kappa-opioid receptors, respectively. The rats treated with omega-CgTx (8-32 pmol i.c.v.) showed transient, dose-dependent shaking behaviour, hyperalgesia and hypothermia which gradually disappeared within 4 h. The behaviour of the rats was normal by 24 h. Histological examination of brain sections showed morphological alterations of neurons in the hippocampus, medial-basal hypothalamus and pyriform cortex. antinociception, catalepsy and thermoregulatory responses elicited by DAMGO (0.4 and 2.0 nmol) were significantly prolonged and potentiated by verapamil (20 pmol i.c.v. 15 min before) or omega-CgTx (8 pmol 24 h before). Antinociception and hypothermia induced by DPDPE were antagonized by verapamil and omega-CgTx, whereas only omega-CgTx prevented the behavioural arousal observed after DPDPE. Similarly, hypothermia induced by dynorphin A-(1-17) (5.0 nmol) and by the kappa-opioid receptor agonist U50,488H (215 nmol) was antagonized by the two Ca2+ channel blockers but only omega-CgTx prevented the barrel rolling and bizarre postures caused by the opioid peptide.

Analgesia↗

PubMed1993

Non-peptide ligands for opioid receptors. Design of kappa-specific agonists.

A series of phenyl carboxyl esters 5a-d derived from N-(cyclopropylmethyl)normetazocine was synthesized and evaluated for its selectivity at mu, kappa, and delta opioid receptors. Compound 5a, although 43 times less potent than the reference compound U50488, was specific for kappa receptors, having no detectable affinity for either mu or delta receptors. Greater binding affinity was seen with the diastereoisomer having the 1'R,2'S stereochemistry in the cyclopropyl ring of the nitrogen substituent, which was only 12 times less active than U50488. Antinociceptive activity in the mouse tail flick was only slightly lower than that of U50488 (ED50 = 7.66 vs 4.52 mg/kg). Naloxone fully prevented antinociception induced by (1'R,2'S)-5a at the doses of 2.0 mg/kg. Compound (1'R,2'S)-5a is one of the most kappa-selective non-peptide compounds reported to date. The implications of these results in terms of requirements for kappa ligands are discussed.

Animals↗