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1.
Oxid Med Cell Longev ; 2020: 1020673, 2020.
Article in English | MEDLINE | ID: mdl-32089764

ABSTRACT

Amyotrophic lateral sclerosis (ALS) is a late-onset neurodegenerative disorder characterized by progressive paralysis resulting from the death of upper and lower motor neurons. There is currently no effective pharmacological treatment for ALS, and the two approved drugs riluzole and edaravone have limited effects on the symptoms and only slightly prolong the life of patients. Therefore, the development of effective therapeutic strategies is of paramount importance. In this study, we investigated whether Miyako Island Bidens pilosa (MBP) can alleviate the neurological deterioration observed in a superoxide dismutase-1 G93A mutant transgenic mouse (G93A mouse) model of ALS. We orally administered 2 g/kg/day of MBP to G93A mice at the onset of symptoms of neurodegeneration (15 weeks old) until death. Treatment with MBP markedly prolonged the life of ALS model mice by approximately 20 days compared to that of vehicle-treated ALS model mice and significantly improved motor performance. MBP treatment prevented the reduction in SMI32 expression, a neuronal marker protein, and attenuated astrocyte (detected by GFAP) and microglia (detected by Iba-1) activation in the spinal cord of G93A mice at the end stage of the disease (18 weeks old). Our results indicate that MBP administered after the onset of ALS symptoms suppressed the inflammatory activation of microglia and astrocytes in the spinal cord of the G93A ALS model mice, thus improving their quality of life. MBP may be a potential therapeutic agent for ALS.


Subject(s)
Amyotrophic Lateral Sclerosis/drug therapy , Drugs, Chinese Herbal/chemistry , Motor Neurons/drug effects , Amyotrophic Lateral Sclerosis/mortality , Animals , Bidens , Disease Models, Animal , Humans , Male , Mice , Mice, Transgenic , Survival Analysis
2.
Yakugaku Zasshi ; 138(12): 1549-1559, 2018.
Article in Japanese | MEDLINE | ID: mdl-30504671

ABSTRACT

Maintaining medication adherence is a critical issue in determining health outcomes in patients with chronic diseases. However, many patients do not adhere to their prescribed regimens. This study aimed to determine the effects of using adherence score sheets according to application timing in improving medication adherence among non-adherent outpatients. In community pharmacies, both patients and pharmacists evaluated medication adherence based on application timing (morning, noon, evening, and before going to bed) in 11 levels (0-10) for >4 months. A total of 58 outpatients were included in the study. The median scores among application timing at intermediate (patient 9.3, pharmacist 9.0) and final (patient 9.5, pharmacist 9.5) analyses were significantly higher than that at baseline (patient 7.6, pharmacist 7.0). At the end of the investigation, the ratio of non-adherent patients prescribed with hyperlipidemic medications was higher than those prescribed with medications for other lifestyle diseases. Approximately 80% of the patients reported improved medication adherence based on the questionnaires regarding their understanding on diseases and medications, medication awareness, and communication with pharmacists. Therefore, the utilization of an adherence score sheet according to application timing improved medication adherence of patients with chronic diseases.


Subject(s)
Medication Adherence/statistics & numerical data , Outpatients/psychology , Outpatients/statistics & numerical data , Awareness , Communication , Cost Savings/methods , Drug Compounding/economics , Drug Compounding/statistics & numerical data , Humans , Hypolipidemic Agents , Japan/epidemiology , Life Style , Prescriptions/economics , Prescriptions/statistics & numerical data , Professional-Patient Relations , Surveys and Questionnaires , Time
3.
Yakugaku Zasshi ; 135(3): 501-6, 2015.
Article in Japanese | MEDLINE | ID: mdl-25759058

ABSTRACT

Much of the damage to health caused by drugs could be prevented by appropriate care. A well-defined duty of care and further information are required for healthcare professionals. Although there are many litigation cases to use as references, neither the extent of the duty of care nor the obligation to explain medication according to the type of drug prescribed has yet been fully established. Thus, we systematically collected decided cases of adverse drug events, and assessed the degree of the duties of care and information. Specifically, we collected decided cases in which physicians, dentists, pharmacists, nurses, or hospitals had been sued. Data were derived from Bessatsu Jurist Iryo-kago Hanrei Hyakusen, Hanrei Jihou, and Hanrei Times from 1989 to November 2013, and information on precedents in the records of the Supreme Court of Japan from 2001 to November 2013. We analyzed the cases, and assessed the following according to the type of drug: (1) standards and explanations when dealing with drugs that were critical issues in litigation, and (2) the degree of the physician's or pharmacist's duties of care and information. In total, 126 cases were collected. The number of drug categories classified was 27, and 9 were considered of practical importance. After this systematic review, we found a trend in the degree of the required level of care and information on several drugs. With respect to duties of care and information, the gap between the required level and actual practice suggests that healthcare professionals must improve their care and explanations.


Subject(s)
Legislation, Drug , Drug-Related Side Effects and Adverse Reactions , Humans , Japan , Pharmacists/legislation & jurisprudence , Professional Role , Time Factors
4.
Biol Pharm Bull ; 32(11): 1928-30, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19881311

ABSTRACT

Involvement of Na+/Ca2+ exchanger (NCX) in pentylenetetrazol (PTZ)-induced convulsion by use of NCX knockout mice and the selective ligand SEA0400 to NCX was examined. In the SEA0400-administered group, the latency to clonic convulsion was extended into 210 s, although the latency to clonic convulsion was observed until 100 s in control group. SEA0400 had little effect on bicuculline-induced clonic seizure nicotine-induced wild running and 4-aminopyridine-induced tonic flexion, respectively. Tonic flexion convulsion was occurred three fifth in the wild type mice group by administration of PTZ, but tonic flexion was not observed in NCX1 knockout mice groups. These results suggest that NCX is involved in inhibitory action in PTZ-induced convulsion.


Subject(s)
Convulsants/toxicity , Pentylenetetrazole/toxicity , Seizures/chemically induced , Sodium-Calcium Exchanger/physiology , Animals , Mice , Mice, Knockout , Seizures/physiopathology , Sodium-Calcium Exchanger/genetics
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