1.Systematic review and Meta-analysis on efficacy and safety of Buzhong Yiqi Decoction for stable chronic obstructive pulmonary disease.
Yi-Ling FAN ; Qing MIAO ; Xing LIAO ; Chang-Zheng FAN ; Mao-Rong FAN ; Qing CAO ; Ning WANG ; Ma QIU-XIAO ; Ya-Ni HAO
China Journal of Chinese Materia Medica 2020;45(22):5344-5355
		                        		
		                        			
		                        			To systematically review the efficacy and safety of Buzhong Yiqi Decoction in the treatment of stable chronic obstructive pulmonary disease(COPD) at the stable stage. Three English databases and four Chinese databases were systematically searched from the database establishment to August 1, 2020. Randomized controlled trials(RCTs) were screened according to the pre-determined inclusion and exclusion criteria, and then the data were extracted. Methodological quality of the included studies was assessed based on Cochrane bias risk tool, and RevMan 5.3 was used for data analysis. A total of 389 articles were retrieved and finally 18 RCTs were included in this study, involving 1 566 patients, and the overall quality of the included studies was not high. Meta-analysis showed that, in terms of improving 6-minute walk distance(6 MWD), and delaying the decline of forced expiratory volume in one second(FEV_1) or its % in the expected value as well as the decline in ratio of FEV_1 to forced vital capacity(FVC), Buzhong Yiqi Decoction alone or in combination with conventional Western medicine was superior to conventional therapy Western medicine alone. Subgroup analysis showed that, in terms of reducing traditional Chinese medicine symptom scores, Buzhong Yiqi Decoction combined with conventional treatment was superior to conventional treatment. In terms of reducing the grade of modified medical research council(mMRC), Buzhong Yiqi Decoction combined with conventional treatment was superior to conventional treatment. In terms of improving 6 MWD, Buzhong Yiqi Decoction combined with conventional treatment or Tiotropium Bromide Powder for Inhalation was superior to conventional treatment alone or Tiotropium Bromide Powder for Inhalation alone. In terms of delaying the decline of FEV_1 or its % in the expected value, Buzhong Yiqi Decoction combined with conventional treatment or Salmeterol Xinafoate and Fluticasone Propionate Powder for Inhalation or Tiotropium Bromide Powder for Inhalation was superior to conventional treatment or Salmeterol Xinafoate and Fluticasone Propionate Powder for Inhalation or Tiotropium Bromide Powder for Inhalation alone, and Buzhong Yiqi Decoction alone was superior to Theophylline alone. In terms of delaying the decline in FEV_1/FVC, Buzhong Yiqi Decoction combined with conventional treatment was superior to conventional treatment, and Buzhong Yiqi Decoction alone was superior to Theophylline alone. Meta-analysis of other outcome measures was not available and no conclusion can be drawn due to the inclusion of only one study. As some studies did not mention the adverse reactions, no safety comments can be made for Buzhong Yiqi Decoction alone or combined with conventional Western medicine. Due to the limitations of the quality and quantity of included studies, the conclusions of this research should be treated with caution. The efficacy of Buzhong Yiqi Decoction for stable COPD still needs more high-quality studies for confirmation, and its safety needs to be further verified.
		                        		
		                        		
		                        		
		                        			Forced Expiratory Volume
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Medicine, Chinese Traditional
		                        			;
		                        		
		                        			Pulmonary Disease, Chronic Obstructive/drug therapy*
		                        			;
		                        		
		                        			Tiotropium Bromide
		                        			;
		                        		
		                        			Vital Capacity
		                        			
		                        		
		                        	
2.Add-on Tiotropium in Chinese Patients With Moderate Asthma: A Pooled Subgroup Analysis of MezzoTinA-Asthma 1 and 2
Jiangtao LIN ; Huanying WAN ; Jian KANG ; Qianli MA ; Ping CHEN ; Meiling JIN ; Haoyan WANG ; Shuang LIU ; Qinglin HAO ; Yong LIN ; Lin SU ; Na HU
Allergy, Asthma & Immunology Research 2019;11(4):519-528
		                        		
		                        			
		                        			PURPOSE: Asthma affects approximately 30 million patients in China; however, tiotropium data for Chinese patients is limited. This study aimed to assess the efficacy and safety of tiotropium in Chinese patients with moderate symptomatic asthma. METHODS: A post hoc subgroup analysis was conducted on 430 Chinese patients pooled from two 24-week, replicate phase 3 trials (NCT01172808 and NCT01172821), in which they received once-daily tiotropium 2.5 µg (Tio R2.5) or 5 µg (Tio R5) (n = 106 or 109, respectively), twice-daily salmeterol 50 µg (Sal 50) (n = 110), or placebo (n = 105), while maintaining inhaled corticosteroids (ICS). The co-primary endpoints assessed in week 24 were forced expiratory volume in 1 second (FEV1) peak0–3h response, trough FEV1 response, and responder rate as assessed using the Asthma Control Questionnaire (ACQ). RESULTS: For both FEV1 peak0–3h responses and trough FEV1 responses, the mean treatment differences were greater for Tio R2.5, Tio R5, and Sal 50 compared with placebo at 0.249 L, 0.234 L, and 0.284 L, and 0.172 L, 0.180 L, and 0.164 L, respectively (P< 0.001). The ACQ responder rate in placebo, Tio R2.5, Tio R5, and Sal 50 was 58.7%, 62.3%, 59.3%, and 69.1%, respectively. Furthermore, 11 (2.6%) of 430 patients had serious adverse events (Tio R5, n = 4; Tio R2.5, n = 1; Sal 50, n = 1; and placebo, n = 5). CONCLUSIONS: Once-daily tiotropium, as add-on to medium-dose ICS, was effective and well tolerated for Chinese patients with moderate symptomatic asthma, consistent with the main analysis.
		                        		
		                        		
		                        		
		                        			Adrenal Cortex Hormones
		                        			;
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Asian Continental Ancestry Group
		                        			;
		                        		
		                        			Asthma
		                        			;
		                        		
		                        			China
		                        			;
		                        		
		                        			Forced Expiratory Volume
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Salmeterol Xinafoate
		                        			;
		                        		
		                        			Tiotropium Bromide
		                        			
		                        		
		                        	
3.Expression of Muscarinic Receptors and the Effect of Tiotropium Bromide in Aged Mouse Model of Chronic Asthma.
Ji Young KANG ; In Kyoung KIM ; Jung HUR ; Seok Chan KIM ; Sook Young LEE ; Soon Seog KWON ; Young Kyoon KIM
Tuberculosis and Respiratory Diseases 2019;82(1):71-80
		                        		
		                        			
		                        			BACKGROUND: Efficacy and safety of tiotropium bromide, a muscarinic receptor antagonist, in treatment of asthma have been reported. However, its effect on airway remodeling in chronic asthma of the elderly has not been clearly verified. The objective of this study was to investigate the effect of tiotropium and expression of muscarinic receptors as its related mechanism in an aged mouse model of chronic asthma with airway remodeling. METHODS: BALB/c female mice age 6 weeks, 9 and 15 months were sensitized and challenged with ovalbumin (OVA) for three months. Tiotropium bromide was administered during the challenge period. Airway hyperresponsiveness (AHR) and pulmonary inflammation were measured. Parameters of airway remodeling, and expression levels of M2 and M3 receptors were examined. RESULTS: Total cell with eosinophils, increased in the OVA groups by age, was decreased significantly after treatment with tiotropium bromide, particularly in the age group of 15 months. AHR and levels of interleukin (IL)-4, IL-5, and IL-13 were decreased, after tiotropium administration. In old aged group of 9- and 15-months-treated groups, hydroxyproline contents and levels of α-smooth muscle actin were attenuated. Tiotropium enhanced the expression of M2 but decreased expression of M3 in all aged groups of OVA. CONCLUSION: Tiotropium bromide had anti-inflammatory and anti-remodeling effects in an aged mouse model of chronic asthma. Its effects seemed to be partly mediated by modulating expression M3 and M2 muscarinic receptors. Tiotropium may be a beneficial treatment option for the elderly with airway remodeling of chronic asthma.
		                        		
		                        		
		                        		
		                        			Actins
		                        			;
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Airway Remodeling
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Asthma*
		                        			;
		                        		
		                        			Eosinophils
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Hydroxyproline
		                        			;
		                        		
		                        			Interleukin-13
		                        			;
		                        		
		                        			Interleukin-5
		                        			;
		                        		
		                        			Interleukins
		                        			;
		                        		
		                        			Mice*
		                        			;
		                        		
		                        			Ovalbumin
		                        			;
		                        		
		                        			Ovum
		                        			;
		                        		
		                        			Pneumonia
		                        			;
		                        		
		                        			Receptors, Muscarinic*
		                        			;
		                        		
		                        			Tiotropium Bromide*
		                        			
		                        		
		                        	
4.Protective effects of cultured and fermented ginseng extracts against scopolamine-induced memory loss in a mouse model.
Song Hee HAN ; Sung June KIM ; Young Won YUN ; Sang Yoon NAM ; Hu Jang LEE ; Beom Jun LEE
Laboratory Animal Research 2018;34(1):37-43
		                        		
		                        			
		                        			This study was performed to investigate the effect of a concentrate of fermented wild ginseng root culture (HLJG0701) on memory improvement in the scopolamine (SPL)-induced memory-deficient mouse model. Eight-week-old male ICR mice were used to evaluate the protective effect of HLJG0701 against the SPL-induced memory loss animal model. The Morris water maze test, which measures hippocampus-dependent learning ability, and the Y-maze test, a short-term memory assessment test, were performed and related markers were analyzed. HLJG0701-treated groups displayed significantly reduced acetylcholinesterase activity and increased acetylcholine level compared with the SPL-administered group (SPL-G) (P < 0.05). In the Y-maze test, the spontaneous alternation in al HLJG0711-treated groups was significantly increased compared with that in SPL-G (P < 0.05). In the Morris water maze test, the escape latency and time spent in the target quadrant in all HLJG0701-treated groups were significantly decreased and increased, respectively, compared with those in SPL-G (P < 0.05). In addition, the brain-derived neurotrophic factor level in groups treated with HLJG0701 300 and 600 mg/kg body weight was significantly increased compared with that in SPL-G (P < 0.05). These results suggest that the HLJG0701 may protect against memory loss by inhibiting acetylcholinesterase activity and preventing acetylcholine deficiency.
		                        		
		                        		
		                        		
		                        			Acetylcholine
		                        			;
		                        		
		                        			Acetylcholinesterase
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Body Weight
		                        			;
		                        		
		                        			Brain-Derived Neurotrophic Factor
		                        			;
		                        		
		                        			Ginsenosides
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Learning
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Memory Disorders*
		                        			;
		                        		
		                        			Memory*
		                        			;
		                        		
		                        			Memory, Short-Term
		                        			;
		                        		
		                        			Mice*
		                        			;
		                        		
		                        			Mice, Inbred ICR
		                        			;
		                        		
		                        			Models, Animal
		                        			;
		                        		
		                        			Panax*
		                        			;
		                        		
		                        			Scopolamine Hydrobromide
		                        			;
		                        		
		                        			United Nations
		                        			;
		                        		
		                        			Water
		                        			
		                        		
		                        	
5.GABA-enriched fermented Laminaria japonica improves cognitive impairment and neuroplasticity in scopolamine- and ethanol-induced dementia model mice.
Storm N S REID ; Je kwang RYU ; Yunsook KIM ; Byeong Hwan JEON
Nutrition Research and Practice 2018;12(3):199-207
		                        		
		                        			
		                        			BACKGROUND/OBJECTIVES: Fermented Laminaria japonica (FL), a type sea tangle used as a functional food ingredient, has been reported to possess cognitive improving properties that may aid in the treatment of common neurodegenerative disorders, such as dementia. MATERIALS/METHODS: We examined the effects of FL on scopolamine (Sco)- and ethanol (EtOH)-induced hippocampus-dependent memory impairment, using the Passive avoidance (PA) and Morris water maze (MWM) tests. To examine the underlying mechanisms associated with neuroprotective effects, we analyzed acetylcholine (ACh) and acetylcholinesterase (AChE) activity, brain tissue expression of muscarinic acetylcholine receptor (mAChR), cAMP response element binding protein (CREB) and extracellular signal-regulated kinases 1/2 (ERK1/2), and immunohistochemical analysis, in the hippocampus of mice, compared to current drug therapy intervention. Biochemical blood analysis was carried out to determine the effects of FL on alanine transaminase (ALT), aspartate transaminase (AST), and triglyceride (TG) and total cholesterol (TC) levels. 7 groups (n = 10) consisted of a control (CON), 3 Sco-induced dementia and 3 EtOH-induced dementia groups, with both dementia group types containing an untreated group (Sco and EtOH); a positive control, orally administered donepezil (Dpz) (4mg/kg) (Sco + Dpz and EtOH + Dpz); and an FL (50 mg/kg) treatment group (Sco + FL50 and EtOH + FL50), orally administered over the 4-week experimental period. RESULTS: FL50 significantly reduced EtOH-induced increase in AST and ALT levels. FL50 treatment reduced EtOH-impaired step-through latency time in the PA test, and Sco- and EtOH-induced dementia escape latency times in the MWM test. Moreover, anticholinergic effects of Sco and EtOH on the brain were reversed by FL50, through the attenuation of AChE activity and elevation of ACh concentration. FL50 elevated ERK1/2 protein expression and increased p-CREB (ser133) in hippocampus brain tissue, according to Western blot and immunohistochemistry analysis, respectively. CONCLUSION: Overall, these results suggest that FL may be considered an efficacious intervention for Sco- and EtOH-induced dementia, in terms of reversing cognitive impairment and neuroplastic dysfunction.
		                        		
		                        		
		                        		
		                        			Acetylcholine
		                        			;
		                        		
		                        			Acetylcholinesterase
		                        			;
		                        		
		                        			Alanine Transaminase
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Aspartate Aminotransferases
		                        			;
		                        		
		                        			Blotting, Western
		                        			;
		                        		
		                        			Brain
		                        			;
		                        		
		                        			Cholesterol
		                        			;
		                        		
		                        			Cognition Disorders*
		                        			;
		                        		
		                        			Cyclic AMP Response Element-Binding Protein
		                        			;
		                        		
		                        			Dementia*
		                        			;
		                        		
		                        			Drug Therapy
		                        			;
		                        		
		                        			Ethanol
		                        			;
		                        		
		                        			Extracellular Signal-Regulated MAP Kinases
		                        			;
		                        		
		                        			Functional Food
		                        			;
		                        		
		                        			Hippocampus
		                        			;
		                        		
		                        			Immunohistochemistry
		                        			;
		                        		
		                        			Laminaria*
		                        			;
		                        		
		                        			Memory
		                        			;
		                        		
		                        			Mice*
		                        			;
		                        		
		                        			Neurodegenerative Diseases
		                        			;
		                        		
		                        			Neuronal Plasticity*
		                        			;
		                        		
		                        			Neuroprotective Agents
		                        			;
		                        		
		                        			Receptors, Muscarinic
		                        			;
		                        		
		                        			Scopolamine Hydrobromide
		                        			;
		                        		
		                        			Triglycerides
		                        			;
		                        		
		                        			United Nations
		                        			;
		                        		
		                        			Water
		                        			
		                        		
		                        	
6.Optimal Bronchodilation for COPD Patients: Are All Long-Acting β₂-Agonist/Long-Acting Muscarinic Antagonists the Same?.
Marc MIRAVITLLES ; Seungjae BAEK ; Vatsal VITHLANI ; Rahul LAD
Tuberculosis and Respiratory Diseases 2018;81(3):198-215
		                        		
		                        			
		                        			Bronchodilators provide improvements in lung function and reductions in symptoms and exacerbations, and are the mainstay of pharmacological management of chronic obstructive pulmonary disease (COPD). The Global Initiative for Chronic Obstructive Lung Disease strategy recommends the use of a combination of long-acting β₂-agonist/long-acting muscarinic antagonists (LABA/LAMA) as the first-line treatment option in the majority of symptomatic patients with COPD. This review provides an indirect comparison of available LABA/LAMA fixed-dose combinations (FDCs) through discussion of important efficacy and safety data from the key literature, with the objective of providing physicians with a framework for informed decision-making. LABA/LAMA FDCs provided greater benefits compared with placebo and similar or greater benefits compared with tiotropium and salmeterol/fluticasone in improving lung function, dyspnea, health-related quality of life, reducing rescue medication use and preventing exacerbations, although with some variability in efficacy between individual FDCs; further, tolerability profiles were comparable among LABA/LAMA FDCs. However, there is a disparity in the amount of evidence generated for different LABA/LAMA FDCs. Thus, this review shows that all LABA/LAMA FDCs may not be the same and that care should be taken when extrapolating individual treatment outcomes to the entire drug class. It is important that physicians consider the efficacy gradient that exists among LABA/LAMA FDCs, and factors such as inhaler devices and potential biomarkers, when choosing the optimal bronchodilator treatment for long-term management of patients with COPD.
		                        		
		                        		
		                        		
		                        			Asian Continental Ancestry Group
		                        			;
		                        		
		                        			Biomarkers
		                        			;
		                        		
		                        			Bronchodilator Agents
		                        			;
		                        		
		                        			Disease Management
		                        			;
		                        		
		                        			Dyspnea
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Korea
		                        			;
		                        		
		                        			Lung
		                        			;
		                        		
		                        			Muscarinic Antagonists*
		                        			;
		                        		
		                        			Nebulizers and Vaporizers
		                        			;
		                        		
		                        			Pulmonary Disease, Chronic Obstructive*
		                        			;
		                        		
		                        			Quality of Life
		                        			;
		                        		
		                        			Tiotropium Bromide
		                        			
		                        		
		                        	
7.Comparison of scopolamine-induced cognitive impairment responses in three different ICR stocks.
Woo Bin YOON ; Hyeon Jun CHOI ; Ji Eun KIM ; Ji Won PARK ; Mi Ju KANG ; Su Ji BAE ; Young Ju LEE ; You Sang CHOI ; Kil Soo KIM ; Young Suk JUNG ; Joon Yong CHO ; Dae Youn HWANG ; Hyun Keun SONG
Laboratory Animal Research 2018;34(4):317-328
		                        		
		                        			
		                        			Cognitive impairment responses are important research topics in the study of degenerative brain diseases as well as in understanding of human mental activities. To compare response to scopolamine (SPL)-induced cognitive impairment, we measured altered parameters for learning and memory ability, inflammatory response, oxidative stress, cholinergic dysfunction and neuronal cell damages, in Korl:ICR stock and two commercial breeder stocks (A:ICR and B:ICR) after relevant SPL exposure. In the water maze test, Korl:ICR showed no significant difference in SPL-induced learning and memory impairment compared to the two different ICRs, although escape latency was increased after SPL exposure. Although behavioral assessment using the manual avoidance test revealed reduced latency in all ICR mice after SPL treatment as compared to Vehicle, no differences were observed between the three ICR stocks. To determine cholinergic dysfunction induction by SPL exposure, activity of acetylcholinesterase (AChE) assessed in the three ICR stocks revealed no difference of acetylcholinesterase activity. Furthermore, low levels of superoxide dismutase (SOD) activity and high levels of inflammatory cytokines in SPL-treated group were maintained in all three ICR stocks, although some variations were observed between the SPLtreated groups. Neuronal cell damages induced by SPL showed similar response in all three ICR stocks, as assessed by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay, Nissl staining analysis and expression analyses of apoptosis-related proteins. Thus, the results of this study provide strong evidence that Korl:ICR is similar to the other two ICR. Stocks in response to learning and memory capacity.
		                        		
		                        		
		                        		
		                        			Acetylcholinesterase
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Brain Diseases
		                        			;
		                        		
		                        			Cognition Disorders*
		                        			;
		                        		
		                        			Cytokines
		                        			;
		                        		
		                        			DNA Nucleotidylexotransferase
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Learning
		                        			;
		                        		
		                        			Memory
		                        			;
		                        		
		                        			Mice
		                        			;
		                        		
		                        			Mice, Inbred ICR
		                        			;
		                        		
		                        			Neurons
		                        			;
		                        		
		                        			Oxidative Stress
		                        			;
		                        		
		                        			Scopolamine Hydrobromide
		                        			;
		                        		
		                        			Superoxide Dismutase
		                        			;
		                        		
		                        			United Nations
		                        			;
		                        		
		                        			Water
		                        			
		                        		
		                        	
8.The Role of Tiotropium+Olodaterol Dual Bronchodilator Therapy in the Management of Chronic Obstructive Pulmonary Disease
Tuberculosis and Respiratory Diseases 2018;81(1):13-18
		                        		
		                        			
		                        			Bronchodilator therapy is central to the management of chronic obstructive pulmonary disease and are recommended as the preferred treatment by the Global Obstructive Lung Disease Initiative (GOLD). Long acting anti-muscarinics (LAMA) and long acting β₂ agonists (LABA) are both more effective than regular short-acting drugs but many patients remain symptomatic despite monotherapy with these drugs. Combination therapy with LAMA and LABA increases the therapeutic benefit while minimizing dose-dependent side effects of long-acting bronchodilator therapy. The TOviTO programme has investigated the benefits of treatment with a combination of tiotropium and olodaterol administered via a single inhaler. Tiotropium+olodaterol 5/5 µg significantly improved forced expiratory volume in 1 second (FEV₁) area under the curve from 0 to 3 hours, trough FEV₁ health status and breathlessness versus the mono-components and placebo. Tiotropium+olodaterol 5/5 µg also increased endurance time and reduced dynamic hyperinflation during constant work rate cycle ergometry. On the basis of these and other studies the 2017 GOLD report recommends escalating to dual bronchodilator therapy in patients in groups B and C if they remain symptomatic or continue to have exacerbations and as initial therapy for patients in group D.
		                        		
		                        		
		                        		
		                        			Dyspnea
		                        			;
		                        		
		                        			Ergometry
		                        			;
		                        		
		                        			Forced Expiratory Volume
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Lung Diseases
		                        			;
		                        		
		                        			Lung Diseases, Obstructive
		                        			;
		                        		
		                        			Nebulizers and Vaporizers
		                        			;
		                        		
		                        			Pulmonary Disease, Chronic Obstructive
		                        			;
		                        		
		                        			Tiotropium Bromide
		                        			
		                        		
		                        	
9.Add-on Therapy for Symptomatic Asthma despite Long-Acting Beta-Agonists/Inhaled Corticosteroid
Michael DREHER ; Tobias MÜLLER
Tuberculosis and Respiratory Diseases 2018;81(1):1-5
		                        		
		                        			
		                        			Asthma, remains symptomatic despite ongoing treatment with high doses of inhaled corticosteroids (ICS) in conjunction with long-acting beta-agonists (LABA), is classified as “severe” asthma. In the course of caring for those patients diagnosed with severe asthma, stepping up from ICS/LABA to more aggressive therapeutic measures would be justified, though several aspects have to be checked in advance (including inhaler technique, adherence to therapy, and possible associated comorbidities). That accomplished, it would be advisable to step up care in accordance with the Global Initiative for Asthma (GINA) recommendations. Possible strategies include the addition of a leukotriene receptor antagonist or tiotropium (to the treatment regimen). The latter has been shown to be effective in the management of several subgroups of asthma. Oral corticosteroids have commonly been used for the treatment of patients with severe asthma in the past; however, the use of oral corticosteroids is commonly associated with corticosteroid-related adverse events and comorbidities. Therefore, according to GINA 2017 these patients should be referred to experts who specialize in the treatment of severe asthma to check further therapeutic options including biologics before starting treatment with oral corticosteroids.
		                        		
		                        		
		                        		
		                        			Adrenal Cortex Hormones
		                        			;
		                        		
		                        			Asthma
		                        			;
		                        		
		                        			Biological Products
		                        			;
		                        		
		                        			Comorbidity
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Immunoglobulin E
		                        			;
		                        		
		                        			Interleukin-5
		                        			;
		                        		
		                        			Nebulizers and Vaporizers
		                        			;
		                        		
		                        			Receptors, Leukotriene
		                        			;
		                        		
		                        			Tiotropium Bromide
		                        			
		                        		
		                        	
10.Drug Abuse and Psychosis: New Insights into Drug-induced Psychosis.
Suji HAM ; Tae Kyoo KIM ; Sooyoung CHUNG ; Heh In IM
Experimental Neurobiology 2017;26(1):11-24
		                        		
		                        			
		                        			Addictive drug use or prescribed medicine abuse can cause psychosis. Some representative symptoms frequently elicited by patients with psychosis are hallucination, anhedonia, and disrupted executive functions. These psychoses are categorized into three classifications of symptoms: positive, negative, and cognitive. The symptoms of DIP are not different from the symptoms of schizophrenia, and it is difficult to distinguish between them. Due to this ambiguity of distinction between the DIP and schizophrenia, the DIP animal model has been frequently used as the schizophrenia animal model. However, although the symptoms may be the same, its causes are clearly different in that DIP is acquired and schizophrenia is heritable. Therefore, in this review, we cover several DIP models such as of amphetamine, PCP/ketamine, scopolamine, and LSD, and then we also address three schizophrenia models through a genetic approach with a new perspective that distinguishes DIP from schizophrenia.
		                        		
		                        		
		                        		
		                        			Amphetamine
		                        			;
		                        		
		                        			Anhedonia
		                        			;
		                        		
		                        			Classification
		                        			;
		                        		
		                        			Executive Function
		                        			;
		                        		
		                        			Hallucinations
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Lysergic Acid Diethylamide
		                        			;
		                        		
		                        			Models, Animal
		                        			;
		                        		
		                        			Psychotic Disorders*
		                        			;
		                        		
		                        			Schizophrenia
		                        			;
		                        		
		                        			Scopolamine Hydrobromide
		                        			;
		                        		
		                        			Substance-Related Disorders*
		                        			
		                        		
		                        	
            
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