نتایج جستجو برای: 6 hydroxy dopamine

تعداد نتایج: 1020826  

2016
Wei Zhou Yibin Zhuang Yanfen Bai Huiping Bi Tao Liu Yanhe Ma

BACKGROUND Type III polyketide synthases (PKSs) contribute to the synthesis of many economically important natural products, which are typically produced by direct extraction from plants or synthesized chemically. For example, humulone and lupulone (Fig. 1a) in hops (Humulus lupulus) account for the characteristic bitter taste of beer and display multiple pharmacological effects. 4-Hydroxy-6-me...

2009
Nitin Verma

22 Effect of Costus speciosus and Wedelia chinensis on Brain Neurotransmitters and Enzyme Monoamine Oxidase Following Cold Immobilization Stress Nitin Verma * and R .L. Khosa Pharmacognosy and Phytochemistry Division, Department of Pharmacy, Bharat Institute of Technology, Partapure Bypass Road Meerut250103, U.P. India ____________________________________________________________________________...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2001
S Fenu V Bassareo G Di Chiara

The involvement of dopamine (DA) in conditioned taste aversion (CTA) learning was studied with saccharin or sucrose as the conditioned stimulus (CS) and intraperitoneal lithium as the unconditioned stimulus (US). The dopamine D(1) antagonist R(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride (SCH 23390) (12.5-50 microg/kg, s.c.), given 5 min after the CS...

1999
NÉSTOR H. GARCÍA THERESA J. BERNDT GERTRUDE M. TYCE FRANKLYN G. KNOX Theresa J. Berndt Gertrude M. Tyce

Garcı́a, Néstor H., Theresa J. Berndt, Gertrude M. Tyce, and Franklyn G. Knox. Chronic oral L-DOPA increases dopamine and decreases serotonin excretions. Am. J. Physiol. 277 (Regulatory Integrative Comp. Physiol. 46): R1476–R1480, 1999.—Given the common pathways for uptake and synthesis for dopamine and serotonin, enhanced renal dopamine synthesis in response to increased substrate 3,4-dihydroxy...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1980
J Houglum J K Pai V Atrache D E Sok C J Sih

Perfusion of cat paws with compound 48/80 released two slow reacting substances (SRSs) which were isolated and characterized as 5-hydroxy-6-S-cysteinylglycyl-7,9,11,14-icosatetraenoic acid (SRS I) and 5-hydroxy-6-S-cysteinyl-7,9,11,14-icosatetraeonic acid (SRS II) on the basis of chemical degradations, amino acid analyses, spectroscopic and enzymic experiments, and comparison with synthetic sam...

Journal: :Pharmacological reports : PR 2010
Alireza M Nayebi Siyamak R Rad Mehdi Saberian Saeid Azimzadeh Morteza Samini

Receptors for 5-HT(1A) are widely distributed throughout the basal ganglia, and their activation results in an inhibition of dopamine (DA) release. This study aimed to investigate the effect of buspirone, as a partial agonist of 5-HT(1A) receptors, on 6-hydroxydopamine (6-OHDA)-induced catalepsy in male Wistar rats. Catalepsy was induced by unilateral infusion of 6-OH-DA (6 microg/2 microl/rat)...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2001
L Calza L Giardino A Giuliani L Aloe R Levi-Montalcini

In postnatal tissues, angiogenesis occurs in nontumoral conditions on appropriate stimuli. In the nervous tissue, hypoxia, neural graft, increased neural function, and synaptic activity are associated with neoangiogenesis. We have investigated the occurrence of neoangiogenesis in the superior cervical ganglia (scg) of newborn rats treated for 8--21 days with 6-hydroxy-dopamine (6-OHDA), nerve g...

2003
Dora Rondina Osvaldo J. Ponzo Berta Szwarcfarb Silvia Carbone Pablo Scacchi

OBJECTIVES: The aim of the present investigation was to determine whether the catecholaminergic system is involved in gabaergic and serotoninergic effects on gonadotrophin secretion during sexual development. To this end, we studied the effect of GABAergic and serotoninergic systems on hypothalamic catecholamine content at different stages of sexual development. METHODS: The effect of GABA A an...

Journal: :Molecular pharmacology 2002
Eldo V Kuzhikandathil Gerry S Oxford

R-(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride (SCH23390) is a widely used, highly selective antagonist of D1 dopamine receptors. While investigating the crosstalk between D1 and D3 dopamine receptor signaling pathways, we discovered that in addition to being a D1 receptor antagonist, SCH23390 and related compounds inhibit G protein-coupled inwardly...

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