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Wyświetlanie 1-2 z 2
Tytuł:
ANTINOCICEPTIVE AND ANTIANXIETY ACTIVITY OF HYDROETHANOLIC EXTRACTS OF THREE IMPATIENS SPECIES IN MICE
Autorzy:
Szewczyk, Katarzyna
Orzelska-Górka, Jolanta
Polakowska, Magdalena
Biała, Grażyna
Powiązania:
https://bibliotekanauki.pl/articles/895511.pdf
Data publikacji:
2018-08-31
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
mice
antinociception
CNS screening
antianxiety
Impatiens
Balsaminaceae
Opis:
The plants of the Impatiens L. (Balsaminaceae) have been used for a long time in folk medicine in different painful conditions, and to treat rheumatism, isthmus and crural aches, fractures, superficial infections, fingernail inflammation. This study was undertaken to determine the pharmacological profile of hydroethanolic extracts from Impatiens glandulifera, I. noli-tangere and I. parviflora. A range of behavioral assessments was applied to evaluate the effects of obtained extracts i.e. measurement of body temperature, tests of locomotor activity and motor coordination, nociceptive reaction and anxiety-like behavior. Hydroethanolic extracts were analyzed for total polyphenol (TPC), flavonoid (TFC), flavones/flavonols (TFFC), and flavonones/dihydroflavonols (TFDC) content. Our results show that the extracts from Impatiens species contain high levels of TPC, TFC, TFFC, and TFDC. Oral (i.e., by gavage) administration of Impatiens L. extracts (except for I. noli-tangere) presented an antinociceptive or/and anti-inflammatory activity in the writhing test. The antinociceptive effect of I. parviflora leaves (100 mg/kg) and I. glandulifera flowers (100 mg/kg) was reversed by naloxone. I. glandulifera flowers and roots extracts (100 mg/kg) increased the reaction time to the thermal stimulus in the hot-plate test. All extracts from I. glandulifera (100 mg/kg) showed antianxiety effect in the elevated plus-maze test. It is worth noting that none of the extracts, at the highest used dose – 0.1 ED50 (200 mg/kg), caused coordination impairments or myorelaxation as measured in the rota-rod and chimney tests. These results seem to suggest that the tested extracts are not neurotoxic.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2018, 75, 4; 989-1001
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The role of FAAH and MAGL inhibitors in anxiety disorders
Autorzy:
Burat, Magdalena
Gibuła-Tarłowska, Ewa
Skiba, Wiktoria
Orzelska-Górka, Jolanta
Kędzierska, Ewa
Powiązania:
https://bibliotekanauki.pl/articles/1030741.pdf
Data publikacji:
2020
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
FAAH inhibitors
MAGL inhibitors
anxiety disorder
endocannabinoids
Opis:
Anxiety disorders are currently one of the most common diseases in industrialized countries, showing a continuous upward trend. Classic therapy was based on GABA receptor modulation. However, numerous side effects associated with the impact on this neurotransmission led to the search for new drugs. The involvement of other messengers like serotonin, dopamine and noradrenaline in the pathophysiology of anxiety disorders, resulted in the introduction of SSRI, SNRI, TLPD and azapirones. However, these drugs are not fully effective, have many limitations and side effects, hence the problem of finding new solutions in anxiety therapy is still valid. One of new theories indicates the role of the endocannabinoid system in the diagnosis and treatment of anxiety. It is well known, that the main endogenous cannabinoids – anandamide (AEA) and 2-arachidonoglicerol (2-AG) – are metabolized by the enzymes from the serine hydrolase group: fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL). This review presents a new compounds form the froup of endocannabinoid degradation inhibitors with anxiolytic activity.
Źródło:
World Scientific News; 2020, 139, 2; 246-258
2392-2192
Pojawia się w:
World Scientific News
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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