Literature DB >> 17585219

Bulleyaconitine A isolated from aconitum plant displays long-acting local anesthetic properties in vitro and in vivo.

Chi-Fei Wang1, Peter Gerner, Sho-Ya Wang, Ging Kuo Wang.   

Abstract

BACKGROUND: Bulleyaconitine A (BLA) is an active ingredient of Aconitum bulleyanum plants. BLA has been approved for the treatment of chronic pain and rheumatoid arthritis in China, but its underlying mechanism remains unclear.
METHODS: The authors examined (1) the effects of BLA on neuronal voltage-gated Na channels in vitro under the whole cell patch clamp configuration and (2) the sensory and motor functions of rat sciatic nerve after single BLA injections in vivo.
RESULTS: BLA at 10 microm did not affect neuronal Na currents in clonal GH3 cells when stimulated infrequently to +50 mV. When stimulated at 2 Hz for 1,000 pulses (+50 mV for 4 ms), BLA reduced the peak Na currents by more than 90%. This use-dependent reduction of Na currents by BLA reversed little after washing. Single injections of BLA (0.2 ml at 0.375 mm) into the rat sciatic notch not only blocked sensory and motor functions of the sciatic nerve but also induced hyperexcitability, followed by sedation, arrhythmia, and respiratory distress. When BLA at 0.375 mm was coinjected with 2% lidocaine (approximately 80 mm) or epinephrine (1:100,000) to reduce drug absorption by the bloodstream, the sensory and motor functions of the sciatic nerve remained fully blocked for approximately 4 h and regressed completely after approximately 7 h, with minimal systemic effects.
CONCLUSIONS: BLA reduces neuronal Na currents strongly at +50 mV in a use-dependent manner. When coinjected with lidocaine or epinephrine, BLA elicits prolonged block of both motor and sensory functions in rats with minimal adverse effects.

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Year:  2007        PMID: 17585219      PMCID: PMC1952535          DOI: 10.1097/01.anes.0000267502.18605.ad

Source DB:  PubMed          Journal:  Anesthesiology        ISSN: 0003-3022            Impact factor:   7.892


  16 in total

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Review 3.  Tricyclic antidepressants and their local anesthetic properties: from bench to bedside and back again.

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4.  Efficacy of lidocaine or bupivacaine combined with ephedrine in rat sciatic nerve block.

Authors:  Yi-Chuan Kau; Yu-Chun Hung; Anthony M Zizza; David Zurakowski; William R Greco; Ging Kuo Wang; Peter Gerner
Journal:  Reg Anesth Pain Med       Date:  2006 Jan-Feb       Impact factor: 6.288

5.  Irreversible block of human heart (hH1) sodium channels by the plant alkaloid lappaconitine.

Authors:  S N Wright
Journal:  Mol Pharmacol       Date:  2001-02       Impact factor: 4.436

6.  Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction.

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8.  The local anesthetic activity of Aconitum alkaloids can be explained by their structural properties: a QSAR analysis.

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9.  L-type calcium channel activation up-regulates the mRNAs for two different sodium channel alpha subunits (Nav1.2 and Nav1.3) in rat pituitary GH3 cells.

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  17 in total

1.  Use of bulleyaconitine A as an adjuvant for prolonged cutaneous analgesia in the rat.

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Review 3.  Structural Advances in Voltage-Gated Sodium Channels.

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4.  Ester Hydrolysis Differentially Reduces Aconitine-Induced Anti-hypersensitivity and Acute Neurotoxicity: Involvement of Spinal Microglial Dynorphin Expression and Implications for Aconitum Processing.

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5.  Bulleyaconitine A attenuates hyperexcitability of dorsal root ganglion neurons induced by spared nerve injury: The role of preferably blocking Nav1.7 and Nav1.3 channels.

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Review 6.  Research progress of aconitine toxicity and forensic analysis of aconitine poisoning.

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Review 7.  Anesthetic Agents of Plant Origin: A Review of Phytochemicals with Anesthetic Activity.

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8.  Bulleyaconitine A Inhibits Visceral Nociception and Spinal Synaptic Plasticity through Stimulation of Microglial Release of Dynorphin A.

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Review 9.  Mechanisms for therapeutic effect of bulleyaconitine A on chronic pain.

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10.  Oral application of bulleyaconitine A attenuates morphine tolerance in neuropathic rats by inhibiting long-term potentiation at C-fiber synapses and protein kinase C gamma in spinal dorsal horn.

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