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Comparative electrophysiological characterization of ammodytoxin A, a β-neurotoxin from the nose-horned viper venom, and its enzymatically inactive mutant
ID
Žužek, Monika C.
(
Avtor
),
ID
Ivanušec, Adrijan
(
Avtor
),
ID
Herman, Julija
(
Avtor
),
ID
Šribar, Jernej
(
Avtor
),
ID
Leonardi, Adrijana
(
Avtor
),
ID
Frangež, Robert
(
Avtor
),
ID
Križaj, Igor
(
Avtor
)
PDF - Predstavitvena datoteka,
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MD5: 282F3E5A8D11BCC29F40211CDEF0D943
URL - Izvorni URL, za dostop obiščite
https://www.sciencedirect.com/science/article/pii/S0041010124004057
Galerija slik
Izvleček
Presynaptic- or β-neurotoxicity of secreted phospholipases A$_2$ (sPLA$_2$) is a complex process. For full expression of β-neurotoxicity, the enzymatic activity of the toxin is essential. However, it has been shown that not all toxic effects of a β-neurotoxin depend on its enzymatic activity, for example, the inhibition of mitochondrial cytochrome c oxidase. The main objective of this study was to verify whether it is possible to observe and study the phospholipase-independent actions of β-neurotoxins by a standard ex vivo twitch-tension experimental approach. To this end, we compared the effects of a potent snake venom β-neurotoxin, ammodytoxin A (AtxA), and its enzymatically inactive mutant AtxA(D49S) on muscle contraction of the mouse phrenic nerve-hemidiaphragm preparation. While AtxA significantly affected the amplitude of the indirectly evoked isometric muscle contraction, the resting tension of the neuromuscular (NM) preparation, the amplitude of the end-plate potential (EPP), the EPP half decay time and the resting membrane potential, AtxA(D49S) without enzymatic activity did not. From this, we can conclude that the effects of AtxA independent of enzymatic activity cannot be studied with classical electrophysiological measurements on the isolated NM preparation. Our results also suggest that the inhibition of cytochrome c oxidase activity by AtxA is not involved in the rapid NM blockade by this β-neurotoxin, but that its pathological consequences are rather long-term. Interestingly, in our experimental setup, AtxA upon direct stimulation reduced the amplitude of muscle contraction and induced contracture of the hemidiaphragm, effects that could be interpreted as myotoxic.
Jezik:
Angleški jezik
Ključne besede:
snake venom
,
ammodytoxin
,
secreted phospholipase A$_2$
,
enzymatic activity
,
cytochrome c oxidase
,
ß-neurotoxicity
,
snakes
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
VF - Veterinarska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2024
Št. strani:
6 str.
Številčenje:
Vol. 247, art. 107833
PID:
20.500.12556/RUL-159212
UDK:
615:616-092:636.09
ISSN pri članku:
1879-3150
DOI:
10.1016/j.toxicon.2024.107833
COBISS.SI-ID:
200247555
Datum objave v RUL:
03.07.2024
Število ogledov:
262
Število prenosov:
61
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Toxicon
Skrajšan naslov:
Toxicon
Založnik:
Elsevier, Brazilian Society of Toxinology, International Society on Toxinology, North American Society of Toxinology
ISSN:
1879-3150
COBISS.SI-ID:
183363843
Licence
Licenca:
CC BY-NC 4.0, Creative Commons Priznanje avtorstva-Nekomercialno 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by-nc/4.0/deed.sl
Opis:
Licenca Creative Commons, ki prepoveduje komercialno uporabo, vendar uporabniki ne rabijo upravljati materialnih avtorskih pravic na izpeljanih delih z enako licenco.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
kačji strup
,
encimska aktivnost
,
strupene kače
Projekti
Financer:
ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:
P1-0207
Naslov:
Toksini in biomembrane
Financer:
ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:
P4-0053
Naslov:
Endokrini, imunski in encimski odzivi pri zdravih in bolnih živalih
Financer:
ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Program financ.:
Young researchers
Številka projekta:
1000-17-0106-6
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