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1.
Egyptian Pharmaceutical Journal [National Research Center]. 2008; 7 (2): 167-176
in English | IMEMR | ID: emr-100906

ABSTRACT

During a careful search for bioactive alkaloidal constituents from the alcoholic extract of Erythrina corallodendron Linn leaves, three alkaloids namely, erysodine [1], erythirinine [2] and 8-oxoerythrinine [3] were isolated. These compounds are reported here for the first time from such species. Structures of the isolated compounds [1-3] were assigned by intensive studies of their NMR and MS spectral data and comparison with related structures. The pharmacological activities of the isolated alkaloids are presented


Subject(s)
Alkaloids/pharmacology , Erythrina , Dihydro-beta-Erythroidine
2.
Biol. Res ; 39(2): 321-330, 2006. ilus, tab
Article in English | LILACS | ID: lil-432434

ABSTRACT

Nicotine exposure is a risk factor in several breathing disorders Nicotinic acetylcholine receptors (nAChRs) exist in the ventrolateral medulla, an important site for respiratory control. We examined the effects of nicotinic acetylcholine neurotransmission on central respiratory control by addition of a nAChR agonist or one of various antagonists into superfusion medium in the isolated brainstem-spinal cord from neonatal rats. Ventral C4 neuronal activity was monitored as central respiratory output, and activities of respiratory neurons in the ventrolateral medulla were recorded in whole-cell configuration. RJR-2403 (0.1-10mM), a4b2 nAChR agonist induced dose-dependent increases in respiratory frequency. Non-selective nAChR antagonist mecamylamine (0.1-100mM), a4b2 antagonist dihydro-b-erythroidine (0.1-100mM), a7 antagonist methyllycaconitine (0.1-100mM), and a-bungarotoxin (0.01-10mM) all induced dose-dependent reductions in C4 respiratory rate. We next examined effects of 20mM dihydro-b-erythroidine and 20mM methyllycaconitine on respiratory neurons. Dihydro-b-erythroidine induces hyperpolarization and decreases intraburst firing frequency of inspiratory and preinspiratory neurons. In contrast, methyllycaconitine has no effect on the membrane potential of inspiratory neurons, but does decrease their intraburst firing frequency while inducing hyperpolarization and decreasing intraburst firing frequency in preinspiratory neurons. These findings indicate that a4b2 nAChR is involved in both inspiratory and preinspiratory neurons, whereas a7 nAChR functions only in preinspiratory neurons to modulate C4 respiratory rate.


Subject(s)
Animals , Rats , Neurons/physiology , Nicotinic Agonists/pharmacology , Nicotinic Antagonists/pharmacology , Receptors, Nicotinic/physiology , Respiratory Center/physiology , Animals, Newborn , Aconitine/analogs & derivatives , Aconitine/pharmacology , Bungarotoxins/pharmacology , Dihydro-beta-Erythroidine/pharmacology , Membrane Potentials , Mecamylamine/pharmacology , Neurons/drug effects , Rats, Wistar , Receptors, Nicotinic/drug effects , Respiratory Center/drug effects
3.
The Korean Journal of Physiology and Pharmacology ; : 219-225, 2004.
Article in English | WPRIM | ID: wpr-727920

ABSTRACT

The pelvic ganglia provide autonomic innervations to the various urogenital organs, such as the urinary bladder, prostate, and penis. It is well established that both sympathetic and parasympathetic synaptic transmissions in autonomic ganglia are mediated mainly by acetylcholine (ACh). Until now, however, the properties of ACh-induced currents and its receptors in pelvic ganglia have not clearly been elucidated. In the present study, biophysical characteristics and molecular nature of nicotinic acetylcholine receptors (nAChRs) were studied in sympathetic and parasympathetic major pelvic ganglion (MPG) neurons. MPG neurons isolated from male rat were enzymatically dissociated, and ionic currents were recorded by using the whole cell variant patch clamp technique. Total RNA from MPG neuron was prepared, and RT-PCR analysis was performed with specific primers for subunits of nAChRs. ACh dose-dependently elicited fast inward currents in both sympathetic and parasympathetic MPG neurons (EC50; 41.4microliterM and 64.0microliterM, respectively). ACh-induced currents showed a strong inward rectification with a reversal potential near 0 mV in current-voltage relationship. Pharmacologically, mecamylamine as a selective antagonist for alpha3beta4 nAChR potently inhibited the ACh-induced currents in sympathetic and parasympathetic neurons (IC50; 0.53micrometer and 0.22micrometer, respectively). Conversely, alpha- bungarotoxin, alpha-methyllycaconitine, and dihydro-beta-erythroidine, which are known as potent and sensitive blockers for alpha7 or alpha4beta2 nAChRs, below micromolar concentrations showed negligible effect. RT-PCR analysis revealed that alpha3 and beta4 subunits were predominantly expressed in MPG neurons. We suggest that MPG neurons have nAChRs containing alpha3 and beta4 subunits, and that their activation induces fast inward currents, possibly mediating the excitatory synaptic transmission in pelvic autonomic ganglia.


Subject(s)
Animals , Humans , Male , Rats , Acetylcholine , Dihydro-beta-Erythroidine , Ganglia , Ganglia, Autonomic , Ganglion Cysts , Mecamylamine , Negotiating , Neurons , Penis , Prostate , Receptors, Nicotinic , Reverse Transcriptase Polymerase Chain Reaction , RNA , Synaptic Transmission , Urinary Bladder
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