TY  - CONF
AU  - Kukić, Jelena
AU  - Savić, Miroslav
AU  - Gavrilović, I.
AU  - Grayer, Rene
AU  - Marin, Petar
AU  - Tomić, Mirko
AU  - Petrović, Silvana
PY  - 2007
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/976
PB  - Georg Thieme Verlag Kg, Stuttgart
C3  - Planta Medica
T1  - Behavioral and chemical characterisation of MeOH extracts of two Stachys taxa
VL  - 73
IS  - 9
SP  - 998
EP  - 998
DO  - 10.1055/s-2007-987343
UR  - https://hdl.handle.net/21.15107/rcub_farfar_976
ER  - 

@conference{
author = "Kukić, Jelena and Savić, Miroslav and Gavrilović, I. and Grayer, Rene and Marin, Petar and Tomić, Mirko and Petrović, Silvana",
year = "2007",
publisher = "Georg Thieme Verlag Kg, Stuttgart",
journal = "Planta Medica",
title = "Behavioral and chemical characterisation of MeOH extracts of two Stachys taxa",
volume = "73",
number = "9",
pages = "998-998",
doi = "10.1055/s-2007-987343",
url = "https://hdl.handle.net/21.15107/rcub_farfar_976"
}

Kukić, J., Savić, M., Gavrilović, I., Grayer, R., Marin, P., Tomić, M.,& Petrović, S.. (2007). Behavioral and chemical characterisation of MeOH extracts of two Stachys taxa. in Planta Medica
Georg Thieme Verlag Kg, Stuttgart., 73(9), 998-998.
https://doi.org/10.1055/s-2007-987343
https://hdl.handle.net/21.15107/rcub_farfar_976

Kukić J, Savić M, Gavrilović I, Grayer R, Marin P, Tomić M, Petrović S. Behavioral and chemical characterisation of MeOH extracts of two Stachys taxa. in Planta Medica. 2007;73(9):998-998.
doi:10.1055/s-2007-987343
https://hdl.handle.net/21.15107/rcub_farfar_976 .

Kukić, Jelena, Savić, Miroslav, Gavrilović, I., Grayer, Rene, Marin, Petar, Tomić, Mirko, Petrović, Silvana, "Behavioral and chemical characterisation of MeOH extracts of two Stachys taxa" in Planta Medica, 73, no. 9 (2007):998-998,
https://doi.org/10.1055/s-2007-987343 .,
https://hdl.handle.net/21.15107/rcub_farfar_976 .

TY  - JOUR
AU  - Vucković, S
AU  - Tomić, M
AU  - Stepanović-Petrović, Radica
AU  - Ugrešić, Nenad
AU  - Prostran, Milica
AU  - Bošković, B
PY  - 2006
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/853
AB  - This study investigated whether carbamazepine could produce local peripheral antinociception in a rat model of inflammatory mechanical hyperalgesia, and whether adenosine receptors are involved. Carbamazepine (100-1000 nmol/paw) coadministrated with a proinflammatory compound, concanavalin A, into the hind paw caused a significant dose- and time-dependent anti-hyperalgesia. Coadministration of caffeine (250 - 1000 nmol/paw), a nonselective adenosine-receptor antagonist, as well as DPCPX (10-30 nmol/paw), a selective adenosine A(1)-receptor antagonist, with carbamazepine, significantly depressed its anti-hyperalgesic effect. Drugs injected into the contralateral hind paw did not produce significant effects. These results suggest that carbamazepine produces local peripheral anti-hyperalgesia via peripheral adenosine A(1) receptors.
PB  - Japanese Pharmacological Soc, Kyoto
T2  - Journal of Pharmacological Sciences
T1  - Peripheral antinociception by carbamazepine in an inflammatory mechanical hyperalgesia model in the rat: a new target for carbamazepine?
VL  - 100
IS  - 4
SP  - 310
EP  - 314
DO  - 10.1254/jphs.SCE05003X
ER  - 

@article{
author = "Vucković, S and Tomić, M and Stepanović-Petrović, Radica and Ugrešić, Nenad and Prostran, Milica and Bošković, B",
year = "2006",
abstract = "This study investigated whether carbamazepine could produce local peripheral antinociception in a rat model of inflammatory mechanical hyperalgesia, and whether adenosine receptors are involved. Carbamazepine (100-1000 nmol/paw) coadministrated with a proinflammatory compound, concanavalin A, into the hind paw caused a significant dose- and time-dependent anti-hyperalgesia. Coadministration of caffeine (250 - 1000 nmol/paw), a nonselective adenosine-receptor antagonist, as well as DPCPX (10-30 nmol/paw), a selective adenosine A(1)-receptor antagonist, with carbamazepine, significantly depressed its anti-hyperalgesic effect. Drugs injected into the contralateral hind paw did not produce significant effects. These results suggest that carbamazepine produces local peripheral anti-hyperalgesia via peripheral adenosine A(1) receptors.",
publisher = "Japanese Pharmacological Soc, Kyoto",
journal = "Journal of Pharmacological Sciences",
title = "Peripheral antinociception by carbamazepine in an inflammatory mechanical hyperalgesia model in the rat: a new target for carbamazepine?",
volume = "100",
number = "4",
pages = "310-314",
doi = "10.1254/jphs.SCE05003X"
}

Vucković, S., Tomić, M., Stepanović-Petrović, R., Ugrešić, N., Prostran, M.,& Bošković, B.. (2006). Peripheral antinociception by carbamazepine in an inflammatory mechanical hyperalgesia model in the rat: a new target for carbamazepine?. in Journal of Pharmacological Sciences
Japanese Pharmacological Soc, Kyoto., 100(4), 310-314.
https://doi.org/10.1254/jphs.SCE05003X

Vucković S, Tomić M, Stepanović-Petrović R, Ugrešić N, Prostran M, Bošković B. Peripheral antinociception by carbamazepine in an inflammatory mechanical hyperalgesia model in the rat: a new target for carbamazepine?. in Journal of Pharmacological Sciences. 2006;100(4):310-314.
doi:10.1254/jphs.SCE05003X .

Vucković, S, Tomić, M, Stepanović-Petrović, Radica, Ugrešić, Nenad, Prostran, Milica, Bošković, B, "Peripheral antinociception by carbamazepine in an inflammatory mechanical hyperalgesia model in the rat: a new target for carbamazepine?" in Journal of Pharmacological Sciences, 100, no. 4 (2006):310-314,
https://doi.org/10.1254/jphs.SCE05003X . .