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    <link>http://repository.usmf.md:80/handle/20.500.12710/363</link>
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    <dc:date>2026-04-14T22:27:28Z</dc:date>
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  <item rdf:about="http://repository.usmf.md:80/handle/20.500.12710/4712">
    <title>Unele efecte ale interacţiunii asocierii izoturon-propranolol cu oxigenul hiperbaric la nivelul metabolismului lipidic</title>
    <link>http://repository.usmf.md:80/handle/20.500.12710/4712</link>
    <description>Title: Unele efecte ale interacţiunii asocierii izoturon-propranolol cu oxigenul hiperbaric la nivelul metabolismului lipidic
Authors: Cheptea, Eduard; Gonciar, Veaceslav
Abstract: In the experiments on rats the effects of the izoturone and propranolol association&#xD;
interaction with hyperbaric oxygen (HBO) on the lipid metabolism level was studied. HBO (6&#xD;
ata 50 min) caused the increase of plasmatic concentration of total lipids, total phospholipids,&#xD;
esterified cholesterol, total lipoproteins, α+γ-lipoproteins, β-lipoproteins and cholesterol of total&#xD;
lipoproteins and of their fractions. Association of the izoturone (20 mg/kg) and propranolol (1,5&#xD;
mg/kg) in normobaric conditions provoked the decrease of the content of total lipids and the&#xD;
increase of concentration of total phospholipids, triglycerids, β-lipoproteins and cholesterol of β-&#xD;
lipoproteins. A complex metabolic interaction of the level of lipidic and lipoproteinic&#xD;
metabolism on the simultaneous prescription of izoturone and propranolol combination and HBO&#xD;
was revealed. In majority of cases the association of izoturone and propranolol and HBO&#xD;
reciprocally normalized the modification of parameters of lipidic metabolism, in some -&#xD;
pharmacological agents act similarly manifasting a tendency of effects accumulation.&#xD;
&#xD;
&#xD;
&#xD;
&#xD;
&#xD;
În experimente pe şobolani au fost studiate efectele interacţiunii asocierii izoturon şi&#xD;
propranolol cu oxigenul hiperbaric (OHB) la nivelul metabolismului lipidic. OHB (6 ata 50 min)&#xD;
a cauzat majorarea concentraţiei plasmatice de lipide totale, fosfolipide totale, colesterol&#xD;
esterificat, lipoproteine totale, α+γ-lipoproteine, β-lipoproteine şi colesterol al lipoproteinelor&#xD;
totale şi fracţiilor lor. Asocierea izoturonului (20 mg/kg) şi propranololului (1,5 mg/kg) în&#xD;
condiţii normobarice a micşorat conţinutul plasmatic de lipide totale şi majorarea concentraţiei&#xD;
de fosfolipide totale, trigliceride, β-lipoproteine şi colesterol al β-lipoproteinelor. La&#xD;
administrarea concomitentă a asocierii izoturonului şi propranololului cu OHB s-a observat o&#xD;
interacţiune complexă la nivelul metabolismului lipidic şi lipoproteic. În majoritatea cazurilor &#xD;
216&#xD;
combinaţia izoturonului cu propranololul şi OHB au normalizat reciproc modificările indicilor&#xD;
metabolismului lipidic, în unele – agenţii farmacologici acţionează similar, manifestând tendinţă&#xD;
de acumulare a efectelor.
Description: Catedra Farmacologie şi farmacie clinică, Centrul Ştiinţific al Medicamentului</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.usmf.md:80/handle/20.500.12710/4711">
    <title>Unele particularităţi farmacologice ale acidului hialuronic</title>
    <link>http://repository.usmf.md:80/handle/20.500.12710/4711</link>
    <description>Title: Unele particularităţi farmacologice ale acidului hialuronic
Authors: Gonciar, Veaceslav; Scutari, Corina; Peredelcu, Rodica; Cazacu, Vasile; Popa, Cristina; Scutari, Oleg
Abstract: Hyaluronic acid can be recommended as a drug for external and parenteral use as a&#xD;
rheological, inflammatory, protective, proliferative, immunomodulatory remedy, for stimulating&#xD;
the synthesis of hemoglobin and as an auxiliary pharmaceutical substance for topical use. Evergrowing&#xD;
needs of AH for pharmaceutical and cosmetic properties require pharmacological&#xD;
investigations and new clinical studies of the AH as auxiliary pharmaceutical substance for the&#xD;
elaboration of medicinal forms in association with other active substances.&#xD;
&#xD;
&#xD;
&#xD;
&#xD;
&#xD;
Acidul hialuronic (AH) este recomandat ca remediu medicamentos cu proprietăți&#xD;
reologice, antiinflamatoare, protective, proliferative, imunomodulatoare, pentru stimularea&#xD;
sintezei hemoglobinei şi în calitate de excipient pentru uz topic. Necesităţile mereu crescânde de&#xD;
AH pentru farmaceutică şi cosmetică impun investigaţii în scopul cercetărilor proprietăţilor &#xD;
212&#xD;
farmacologice noi, testării clinice a AH în calitate de substanţă farmaceutică auxiliară pentru&#xD;
elaborarea formelor medicamentoase în asociaţie cu alte substanţe active.
Description: Catedra Farmacologie şi farmacie clinică&#xD;
Dispensarul Dermatovenerologic Municipal</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.usmf.md:80/handle/20.500.12710/4713">
    <title>Proprietăţile adsorbante ale enterosorbantului Medicas E</title>
    <link>http://repository.usmf.md:80/handle/20.500.12710/4713</link>
    <description>Title: Proprietăţile adsorbante ale enterosorbantului Medicas E
Authors: Bodrug, Elena
Abstract: In experiments on rats were studied the efficiency of carbon activated Medicas E in acute&#xD;
poisoning with amitriptyline, propranolol, isoniazid and digoxin. The adsorbent Medicas E&#xD;
prevents the development of seizures and death in rats with acute amitriptyline intoxication.&#xD;
Medicas E, compared with medicinal coal, showed more marked beneficial effects in poisoning&#xD;
with propranolol, isoniazid and digoxin, manifested by significantly increasing of the latent&#xD;
period of convulsions and death, and by reduction of animal lethality in 40-90% cases.&#xD;
&#xD;
&#xD;
&#xD;
&#xD;
&#xD;
În experimente pe şobolani a fost studiată eficacitatea cărbunelui activ Medicas E în&#xD;
intoxicaţia acută cu amitriptilină, propranolol, isoniazidă şi digoxină. Adsorbantul Medicas E a&#xD;
preîntâmpinat dezvoltarea convulsiilor şi decesul şobolanilor în intoxicaţia acută cu amitriptilină.&#xD;
Medicas E, în comparaţie cu cărbunele medicinal, a manifestat efecte benefice mai marcate în&#xD;
intoxicaţia cu propranolol, isoniazidă şi digoxină, manifestate prin creşterea semnificativă a&#xD;
perioadei latente a convulsiilor şi a decesului, precum şi prin reducerea cu 40-90% a letalităţii&#xD;
animalelor.
Description: Catedra Farmacologie şi farmacie clinică, USMF “Nicolae Testemiţanu”</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.usmf.md:80/handle/20.500.12710/4707">
    <title>Realizări şi perspective în tratamentul diabetului zanarat tip 2</title>
    <link>http://repository.usmf.md:80/handle/20.500.12710/4707</link>
    <description>Title: Realizări şi perspective în tratamentul diabetului zanarat tip 2
Authors: Bacinschi, Nicolae; Ghicavîi, Victor; Baltag, Natalia; Bacinschi, Aurelia; Morneală, Elena
Abstract: The rational selection of oral antidiabetics in diabetes mellitus treatment, type II is&#xD;
determined by the influence upon pathogenic way, prevention of insulinoresistance and insulin&#xD;
secretion insufficiency. With this purpose theare can be utilized sulphonylureics (glyclazide,&#xD;
glypizide, glymepiride etc.), biguanides (metphormine), meglytinedes (repaglynide, nateglynide,&#xD;
mitiglynide), thyazolidindiones (pioglytazone, balaglyztazone, rivoglitazone etc.), dual/pan&#xD;
PPAR modulators ( tesaglitazar, muraglitazar, aleglitazar, chiglitazar etc.), tetrazaharides&#xD;
(acarboze, vogliboze etc.), GLP-1 agonists (exenatide, exenatide LAR, liraglutide, albiglutide&#xD;
etc.), DPP-IV antagonists and blockers (sitaglypide, vildaglyptide, saxaglyptine, aloglyptine),&#xD;
amilines analogues (pramlintid), selective sodium glucose cotransporter-2 inhibitors&#xD;
(dapagliflozin, canagliflozin, empagliflozin etc.), 11-beta-hydroxysteroid dehydrogenase type 1&#xD;
inhibitors (INCB13739), situins (resveratrol etc.), AMP-activated protein kinase (imeglimin&#xD;
etc.), glucokinase activators (piragliatin etc.), agonists D2-receptors (bromcriptine), bile acid&#xD;
sequestrants (coleselevam) etc..&#xD;
&#xD;
&#xD;
&#xD;
&#xD;
&#xD;
Selectarea raţională a antidiabeticelor orale în tratamentul diabetului zaharat tip 2 este&#xD;
determinată de influenţa asupra verigelor patogenetice, combaterea insulinorezistenţei şi&#xD;
insuficienţei secreţiei insulinei. Cu acest svop se pot utiliza: sulfonilureicele (gliclazida,&#xD;
glipizida, glimepirida etc.), biguanidele (metformina), meglitinidele (repaglinida, nateglinida,&#xD;
mitiglinida), tiazolidindionele (pioglitazon, balaglitazon, rivoglitazon etc.), modulatorii bi-şi pan&#xD;
ai PPAR receptorilor (tesaglitazar, muraglitazar, aleglitazar, cicglitazar etc.), tetrazaharidele&#xD;
(acarboza, vogliboza etc.), agoniştii GLP-1 (exenatid, exenatid LAR, liraglutid, albiglutid etc.),&#xD;
antagoniştii sau blocantele DPP-IV (sitagliptina, vildagliptina, saxagliptina, alogliptina etc.),&#xD;
analogii amilinei (pramlintid), inhibitorii sodiu-glucoză cotransportorului 2 (dalagliflozin,&#xD;
canagliflozin, empagliflozin etc.), inhibitorii 11-beta-hidroxisteroid dehidrogenazei 1&#xD;
(INCB13739), sirtuinele (resveratrol etc.), activatorii AMP-protein kinazei (imeglimin etc.),&#xD;
activatorii glucokinazei (piragliatin etc.), agoniştii D2-receptorilor (bromocriptina etc.),&#xD;
sechestranţii acizilor biliari (coleselevam etc.) etc..
Description: USMF „Nicolae Testemiţanu”, catedra farmacologie şi farmacologie clinică&#xD;
IMSP SCM „Sfânta Treime”&#xD;
IMSP Centrul Republican de Diagnosticare Medicală</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
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