Dose- and duration-dependent effects of betahistine dihydrochloride treatment on histamine turnover in the cat
-
Add time:08/22/2019 Source:sciencedirect.com
Drugs interacting with the histaminergic system are currently used for vertigo treatment and it was shown in animal models that structural analogues of histamine like betahistine improved the recovery process after vestibular lesion. This study was aimed at determining the possible dose and duration effects of betahistine treatment on histamine turnover in normal adult cats, as judged by the level of messenger RNA for histidine decarboxylase (enzyme synthesizing histamine) in the tuberomammillary nuclei. Experiments were conducted on betahistine-treated cats receiving daily doses of 2, 5, 10, or 50 mg/kg during 1 week, 3 weeks, 2 months, or 3 months. The 1-week, 3-week, and 2- and 3-month treatments correspond to the acute, compensatory, and sustained compensatory stages of vestibular compensation, respectively. The lowest dose (2 mg/kg) given the longest time (3 months) was close to the dosage for vestibular defective patients. Data from the experimental groups were compared to control, untreated cats and to placebo-treated animals.The results clearly show that betahistine dihydrochloride administered orally in the normal cat interferes with histamine turnover by increasing the basal expression level of histidine decarboxylase mRNA of neurons located in the tuberomammillary nuclei of the posterior hypothalamus. The effects were both dose- and time-dependent.In conclusion, compensation of both static and dynamic deficits is subtended by long-term adaptive mechanisms that could be facilitated pharmacologically using betahistine dihydrochloride.
We also recommend Trading Suppliers and Manufacturers of Histidine dihydrochloride (cas 15474-90-5). Pls Click Website Link as below: cas 15474-90-5 suppliers
Prev:ArticleHistidine-Dependent Protein Methylation Is Required for Compartmentalization of CTP Synthase
Next:Original articleStructural and functional changes in RNAse A originating from tyrosine and histidine cross-linking and oxidation induced by singlet oxygen and peroxyl radicals) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Research ArticlePharmaceutical BiotechnologyThe Use of a 2,2'-Azobis (2-Amidinopropane) Dihydrochloride Stress Model as an Indicator of Oxidation Susceptibility for Monoclonal Antibodies08/25/2019
- Solubility of L-histidine in different aqueous binary solvent mixtures from 283.15 K to 318.15 K with experimental measurement and thermodynamic modelling08/24/2019
- Original articleStructural and functional changes in RNAse A originating from tyrosine and histidine cross-linking and oxidation induced by singlet oxygen and peroxyl radicals08/23/2019
- ArticleHistidine-Dependent Protein Methylation Is Required for Compartmentalization of CTP Synthase08/21/2019
- Binary diffusion coefficients of l-histidine methyl ester dihydrochloride in aqueous solutions08/20/2019
- Growth and characterization of α and β form of L-Histidine dihydrochloride (cas 15474-90-5) single crystals08/19/2019


