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32results about How to "Improve movement disorders" patented technology

Methods of administering amantadine

ActiveUS20150087721A1Functional difficultyHigh concentrationBiocideGranular deliveryMedicineAmantadine
Methods of nighttime administration of amantadine to reduce sleep disturbances in patient undergoing treatment with amantadine are described, as well as compositions of extended release amantadine that are suitable for nighttime administration.
Owner:ADAMAS PHARMA LLC

Method for avoiding moving obstacle in UUV navigation process based on virtual puffing

The invention discloses a method for avoiding a moving obstacle in a UUV navigation process based on virtual puffing, and relates to the method for avoiding the moving obstacle in the UUV navigation process. The invention aims at solving a problem that a conventional moving obstacle avoiding method is difficult to predict the moving state of a random moving obstacle accurately. The method comprises the steps: firstly determining that an UUV and the moving obstacle navigate in opposite directions or in the same direction, adjusting the heading of the UUV through employing a puffing and rectangular virtual obstacle when the UUV and the moving obstacle navigate in opposite directions, and avoiding the moving obstacle, wherein the navigation in the same direction comprises two types: the UUV follows the moving obstacle and the moving obstacle follows the UUV; adjusting the heading of the UUV through employing the puffing and rectangular virtual obstacle when the UUV follows the moving obstacle, and avoiding the moving obstacle; enabling the UUV to continuously adjust the moving speed when the moving obstacle follows the UUV, adjusting the heading of the UUV through employing the puffing and rectangular virtual obstacle, and avoiding the moving obstacle. The method is used in the field of moving obstacle avoiding of UUVs.
Owner:HARBIN ENG UNIV

Composition and method for treating neurological disease

ActiveUS10213393B1Increases number of awake ON hour without dyskinesiaIncrease the number ofNervous disorderPill deliveryDiseaseNeurological disorder
The present disclosure is directed to methods of treating neurological disorders in a patient such as Parkinson's disease, drug-induced extrapyramidal reactions, and / or levodopa-induced dyskinesia comprising administering to the patient once daily in the morning a pharmaceutical composition comprising about 50 mg to about 400 mg of extended-release amantadine or a pharmaceutically acceptable salt thereof.
Owner:ADAMAS PHARMA INC

Novel agents for ameliorating motor disorder

A novel medicament for treating neurodegenerative diseases, especially for ameliorating dyskinesia, comprising as an active ingredient selenoprotein P and / or a peptide fragment or a series of peptide fragments derived from said protein is provided. The novel medicament for treating neurodegenerative diseases, especially for ameliorating dyskinesia, according to the present invention is suitably applicable to diseases with decrease in motor function.
Owner:JURIDICAL FOUND THE CHEMO SERO THERAPEUTIC RES INST

Huntingdon disease (HD)-targeted proteins and their coding genes and use

The invention relates to the field of gene engineering and especially relates to Huntingdon disease (HD)-targeted proteins and their coding genes and use. The HD-targeted genes provided by the invention comprise Ctrl, ATP7A and ATP7B, and through gene silencing interference of Ctrl or overexpression of ATP7A and ATP7B, HD patient symptoms are obviously relieved or HD occurrence is delayed. According to the invention, the human HD-targeted proteins have amino acid sequences shown in the formulas of SEQ ID No.5, SEQ ID No.6, SEQ ID No.7, SEQ ID No.8 and SEQ ID No.9. The genes have nucleotide sequences shown in the formulas of SEQ ID No.10, SEQ ID No.11, SEQ ID No.12, SEQ ID No.13 and SEQ ID No.14. Through gene silencing or gene overexpression, the targeted genes can be used for improving HD patient athletic ability, prolonging a HD patient life, and relieving or preventing cut huntingtin (htt) deposition in the brain and htt deposition-caused nerve degeneration. The invention provides a novel treatment approach and key target positions for HD.
Owner:TSINGHUA UNIV

Composition and method for treating neurological disease

ActiveUS10213394B1Increases number of awake ON hour without dyskinesiaIncrease the number ofNervous disorderPill deliveryNeurological disorderDisease cause
The present disclosure is directed to methods of treating neurological disorders in a patient such as Parkinson's disease, drug-induced extrapyramidal reactions, and / or levodopa-induced dyskinesia comprising administering to the patient once daily in the morning a pharmaceutical composition comprising about 50 mg to about 400 mg of extended-release amantadine or a pharmaceutically acceptable salt thereof.
Owner:ADAMAS PHARMA INC

Methods of treating patients suffering from movement disorders

InactiveUS7727994B2Reducing and suppressing adverse effectiveness of L-DOPAShorten closing timeBiocideNervous disorderDisease patientAdenosine a
The present invention is directed to methods of treating movement disorders by administering an effective amount of one or more adenosine A2A receptor antagonists to a patient in need thereof. The present invention also provides methods of decreasing the adverse effects of L-DOPA in patients receiving L-DOPA therapy in the treatment of Parkinson's disease. The present invention further provides methods and compositions for treating Parkinson's disease patients with sub-clinically effective doses of L-DOPA by combining L-DOPA treatment with an effective amount of one or more adenosine A2A receptor antagonists (i.e., L-DOPA sparing effect). The present invention further provides methods of effective treatment of Parkinson's disease by co-administering at least one adenosine A2A receptor antagonist, L-DOPA and a dopamine agonist and / or a COMT inhibitor and / or a MAO inhibitor. The present invention further provides methods of prolonging effective treatment of Parkinson's disease by administering an adenosine A2A receptor antagonist singly or together with a dopamine agonist, and / or a COMT inhibitor, and / or a MAO inhibitor without prior or subsequent administration of L-DOPA, delaying or removing on-set of L-DOPA motor complication.
Owner:KYOWA HAKKO KIRIN CO LTD

Chinese medicine fumigation composition for adjunctive therapy of spastic cerebral palsy

The invention relates to a Chinese medicine fumigation composition for the adjunctive therapy of spastic cerebral palsy, comprising 24-45 parts of Astragalus mongholicus, 12-18 parts of angelica sinensis, 9-15 parts of Ligusticum wallichii, 6-12 parts of lumbricus, 9-15 parts of peach seed, 12-18 parts of safflower, 12-18 parts of red peony root, 9-15 parts of radix curcumae, 9-15 parts of polygala tenuifolia, 12-18 parts of lycopodium clavatum, 12-18 parts of phryma leptostachya, and 9-18 parts of mulberry twig. According to the invention, the Chinese medicine fumigation composition disclosed herein uses the therapeutic principle of tonifying qi and removing blood stasis, wherein Astragalus mongholicus is used as main medicine for tonifying qi of spleen and stomach to activate qi to promote blood circulation, remove blood stasis without damage healthy qi, and assist the effects of herbs; angelica sinensis, Ligusticum wallichii, peach seed, safflower, and red peony root are used as auxiliary medicines for activating blood and removing stasis; lumbricus, lycopodium clavatum, and phryma leptostachya are used for clearing and activating the channels and collaterals, radix curcumae and polygala tenuifolia are used for activating blood circulation and inducing resuscitation, and mulberry twig is used for lubricating joints and restricting warm dryness of herbs, all the herbs play an effect of tonifying qi, activating blood circulation, inducing resuscitation, and relaxing muscles and tendons, thus the purpose of relieving muscular tension is achieved, and dyskinesia of the patient is obviously improved or eliminated.
Owner:ZHENGZHOU MATERNAL & CHILD HEALTH HOSPITAL

Traditional Chinese medicine preparation for treating Parkinson's disease

The invention is concerned with the Chinese traditional medicine preparation for treating Parkinsonism. The active constituent of preparation is with the following weight ratio: prepared rhizome of rehmannia is 20g to 30g, medlar is 15g to 20g, ginseng is 8g to 10g, radix salviae miltiorrhizae is 20g to 30g, dragon's blood is 10g to 15g, bloodsucker is 8g to 12g, gastrodia elata is 15g to 20g, gouteng is 20g to 30g, arisaema cum bile is 10g to 12g, alisma is 12g to 15g, a ristolochia recurvilabra is 10g to 15g, agilawood is 8g to 10g, storax is 8g to 10g. The invention is with better curative effect.
Owner:韩立廷

Application of ferroptosis inhibitor in preparation of preparation for improving motion function of aged individuals

The invention discloses an application of a ferroptosis inhibitor in preparation of a preparation for improving the motion function of aged individuals. Through transcriptome sequencing analysis, Tfr1 expression in skeletal muscle and muscle satellite cells is reduced along with age increase. The specific knockout of the Tfr1 muscle satellite cells leads to irreversible inactivation of the muscle satellite cells. The skeletal muscle regeneration process of the Tfr1 muscle satellite cell specific mouse is accompanied by amyotrophy, iron ion accumulation and increase of unsaturated fatty acid biosynthesis, and then skeletal muscle ferroptosis is induced. The senescent skeletal muscle shows that the expression of Tfr1 is reduced, and the surface of an Slc39a14 membrane is enriched, so that the absorption of non-iron transporter binding iron is promoted to be increased, and the occurrence of ferroptosis is promoted. By intraperitoneal injection of the Ferrostatin-1 into aged mice, muscle aplastic disorder and dyskinesia caused by skeletal muscle ferroptosis can be remarkably improved.
Owner:GUANGDONG INST OF MICROBIOLOGY GUANGDONG DETECTION CENT OF MICROBIOLOGY +1

Application of PDE (phosphodiesterase)4 inhibitor

InactiveCN107412214ARepair degenerationRepair oxidative damageOrganic active ingredientsNervous disorderNeuronal damagePDE4 Inhibitors
The invention discloses an application of a PDE (phosphodiesterase)4 inhibitor. The PDE4 inhibitor is FCPR16, and the structural formula of the inhibitor is represented in the description; FCPR16 is applied to preparation of drugs for preventing or treating PD (Parkinson's disease) or applied to preparation of drugs for repairing dopaminergic neuron damage. The application of the inhibitor in preparation of drugs for treating PD is disclosed for the first time, the new application field of the PDE4D inhibitor FCPR16 is expanded, and the inhibitor has good effect on dyskinesia of PD; the inhibitor can repair retrogression, apoptosis or oxidative damage of dopaminergic neurons.
Owner:兰晟生物医药(苏州)有限公司

Composition and method for treating neurological disease

InactiveUS20190247331A1Increases number of awake ON hour without dyskinesiaIncrease the number ofNervous disorderAmine active ingredientsDiseaseNeurological disorder
The present disclosure is directed to methods of treating neurological disorders in a patient such as Parkinson's disease, drug-induced extrapyramidal reactions, and / or levodopa-induced dyskinesia comprising administering to the patient once daily in the morning a pharmaceutical composition comprising about 50 mg to about 400 mg of extended-release amantadine or a pharmaceutically acceptable salt thereof.
Owner:ADAMAS PHARMA INC

Micromolecule polypeptide and application thereof to preparation of medicines for preventing and treating Parkinson's disease

The invention discloses micromolecule polypeptide TAT-PSYN and an application thereof to preparation of medicines for preventing or treating Parkinson's disease. Through synthesizing a TAT protein transduction domain and combining and restraining fusion protein TAT-pSyn of protein polypeptide of alpha-synuclein (alpha-synuclein), pSyn protein polypeptide carried through TAT passes through blood-brain barriers through blood transportation and is taken in by nerve cells. The polypeptide is applied to an Alpha-synuclein(A53T) transgenic Parkinson mouse model, so that the effect of the polypeptidefor blocking combination of alpha-synuclein (alpha-synuclein) and death associated protein kinase 1 (DAPK1) can be effectively exerted, loss of dopaminergic neurons and nerve projection, caused by alpha-synuclein phosphorylation and abnormal gathering can be restrained, the dyskinesia of the Parkinson model is reduced, and a molecular target is provided for medicines for clinical treatment of theParkinson's disease.
Owner:HUAZHONG UNIV OF SCI & TECH

Application of indole-3-carbinol, diindolyl methane and derivatives thereof in preparation of medicaments for treating senile dementia

The invention provides new application of indole-3-carbinol (I3C), diindolyl methane (DIM) and derivative compounds thereof in preparation of medicaments for treating senile dementia. By improving the expression of intracellular free radical resistant specific genes, the medicaments can enhance the automatic free radical clearing capacity of cells and lighten the harm of free radicals to the cells and tissues. The DIM, the I3C and the derivative compounds can effectively reduce the pathogenetic symptoms of senile dementia animal models, obviously improve the dyskinesia of SAM-P / 8 mice, obviously improve the superoxide dismutase (SOD) activity of brain tissues of the SAM-P / 8 mice, reduce the methylene dioxyamphetamine (MDA) content of brain tissues, reduce the choline esterase activity of the brain tissues and enhance the activities of Na<+>-K<+>-ATP enzyme and Ca<2+>-ATP enzyme of the brain tissues, so the DIM, the I3C and the derivative compounds can be used as candidate medicament molecules for treating the senile dementia. Meanwhile, the adopted small molecular substances are easily obtained, are low in price, stable in properties and convenient for storage and transportation, and have broad application prospect.
Owner:合肥硕健医药科技有限公司

Application of osteocalcin or propanoic acid to preparation of anti-parkinson's disease drug

The invention relates to an application of osteocalcin or propanoic acid to preparation of an anti-parkinson's disease drug. The invention finds that dyskinesia of a mouse model of a parkinson's disease and damage to dopaminergic neurons can be improved through osteocalcin or propanoic acid intervention on the mouse model of the parkinson's disease; and the finding suggests that the osteocalcin orpropanoic acid has the potential to be a drug to improve the parkinson's disease.
Owner:RUIJIN HOSPITAL AFFILIATED TO SHANGHAI JIAO TONG UNIV SCHOOL OF MEDICINE +1

New use of phenytoin sodium

InactiveCN105769858AInhibition and relief of movement disordersImprove movement disordersOrganic active ingredientsNervous disorderDrugUnilateral lesion
The invention relates to new use of phenytoin sodium. According to the new use, through injecting the phenytoin sodium into a rat body through intraperitoneal injection, improved conditions on dyskinesia of a 6-hydroxy-dopamine unilateral-lesion PD (Parkinson's Disease) rat model are observed from praxiology, so that application of phenytoin sodium in the preparation of drugs for relieving PD motor symptoms is sought. The novel drugs for treating PD, created by the invention, provide research carriers for researching the molecular mechanism of PD and dyskinesia and meanwhile provide a screening platform for the research and development of the novel drugs for treating PD.
Owner:SHANGHAI UNIV

Composition and method for treating neurological disease

ActiveUS20190247328A1Improve movement disordersIncreases number of awake ON hour without dyskinesiaNervous disorderPill deliveryPharmaceutical drugPharmaceutical medicine
The present disclosure is directed to methods of treating neurological disorders in a patient such as Parkinson's disease, drug-induced extrapyramidal reactions, and / or levodopa-induced dyskinesia comprising administering to the patient once daily in the morning a pharmaceutical composition comprising about 50 mg to about 400 mg of extended-release amantadine or a pharmaceutically acceptable salt thereof.
Owner:ADAMAS PHARMA INC

Traditional Chinese medicine composition for treating lumbar disc herniation with kidney deficiency and blood stasis and a preparation method thereof

The invention relates to a traditional Chinese medicine composition for treating lumbar disc herniation with kidney deficiency and blood stasis and a preparation method thereof, and belongs to the field of traditional Chinese medicines. The traditional Chinese medicine composition is prepared from the following raw materials in parts by weight: 25-35 parts of rehmannia glutinosa, 20-30 parts of herba pyrolae, 18-22 parts of epimedium, 18-22 parts of oyster, 9-11 parts of radix clematidis, 9-11 parts of sun-cured dog bone, 9-11 parts of tuckahoe, 9-11 parts of siegesbeckia pubescens, 1.1-1.3 parts of borneol. The composition has the advantages of clearing and activating the channels and collaterals, removing stasis and relieving pain, is mainly used for treating lumbar spinal stenosis, lumbar disc herniation, and sciatica, and is developed to be a preparation in the affiliated hospital of Changchun University of Chinese medicine for mainly treating waist and leg pain caused by lumbar spinal stenosis, and after clinical application of the composition for many years, a large number of patients with lumbar disc herniation after administration show good therapeutic effects.
Owner:CHANGCHUN UNIV OF CHINESE MEDICINE

Rehabilitation support device and rehabilitation support method

Provided is a rehabilitation support device for supporting rehabilitation of a user having impaired mobility, configured to effectively improve the user's mobility by supporting the rehabilitation. This rehabilitation support device is provided with: a request unit for requesting a target movement to be performed in a three-dimensional space; and a feedback unit for sending, approximately simultaneously with the completion of the target movement, feedback that stimulates at least two of five senses, the feedback being sent to the user who has performed the target movement.
Owner:MEDIVR INC

Application of iron transporter in treatment of Parkinson's disease

The invention relates to the field of gene engineering, in particular to a target protein of Parkinson's disease (PD) and an encoding gene and application thereof, and particularly relates to preparation of a gene targeting drug aiming at the key gene. The target protein finds that a target gene ZIP13 and Transferrin (Tsf) for Parkinson's disease are provided, and the PD condition is remarkably relieved or delayed by over-expressing the ZIP13 or interfering the Tsf through gene silencing. According to the target protein the human PD target protein comprises amino acid sequences represented bySEQ ID No. 5 and SEQ ID No. 6, and the gene comprises nucleotide sequences represented by SEQ ID No. 7 and SEQ ID No. 8. According to the target gene, an RNAi vector carrying a target gene is constructed, and the athletic ability of a PD patient can be improved through gene silencing or gene overexpression, and PD symptoms caused by knockdown of PINK1 is relieved or prevented. The target protein is expected to provide a novel treatment strategy and a key target for treating hereditary PD.
Owner:HEFEI UNIV OF TECH

A motion obstacle avoidance method during uuv navigation based on virtual puffing

The invention discloses a method for avoiding a moving obstacle in a UUV navigation process based on virtual puffing, and relates to the method for avoiding the moving obstacle in the UUV navigation process. The invention aims at solving a problem that a conventional moving obstacle avoiding method is difficult to predict the moving state of a random moving obstacle accurately. The method comprises the steps: firstly determining that an UUV and the moving obstacle navigate in opposite directions or in the same direction, adjusting the heading of the UUV through employing a puffing and rectangular virtual obstacle when the UUV and the moving obstacle navigate in opposite directions, and avoiding the moving obstacle, wherein the navigation in the same direction comprises two types: the UUV follows the moving obstacle and the moving obstacle follows the UUV; adjusting the heading of the UUV through employing the puffing and rectangular virtual obstacle when the UUV follows the moving obstacle, and avoiding the moving obstacle; enabling the UUV to continuously adjust the moving speed when the moving obstacle follows the UUV, adjusting the heading of the UUV through employing the puffing and rectangular virtual obstacle, and avoiding the moving obstacle. The method is used in the field of moving obstacle avoiding of UUVs.
Owner:HARBIN ENG UNIV

A small molecular polypeptide and its application in the preparation of drugs for preventing and treating Parkinson's syndrome

The invention discloses a small molecule polypeptide TAT‑PSYN and its application in the preparation of drugs for preventing or treating Parkinson's syndrome. By synthesizing the fusion protein TAT-pSyn of the TAT protein transduction domain and the protein polypeptide that can bind to and inhibit the synuclein (alpha-synuclein), the pSyn protein polypeptide is transported through the blood through the blood-brain barrier by TAT, and is neuron Yuan uptake. Applying the polypeptide to the Alpha‑synuclein (A53T) transgenic mouse model of Parkinson’s disease can effectively block the combination of synuclein (alpha‑synuclein) and death-associated protein kinase 1 (DAPK1), and inhibit the α‑synuclein (alpha‑synuclein) The loss of dopamine neurons and nerve projections caused by synuclein phosphorylation and abnormal aggregation can reduce the dyskinesia of Parkinson's model, and provide molecular targets for clinical treatment of Parkinson's syndrome drugs.
Owner:HUAZHONG UNIV OF SCI & TECH

Application of ferroportin in the treatment of Parkinson's disease

The present invention relates to the field of genetic engineering, in particular, the present invention relates to a target protein of Parkinson's Disease (PD) and its encoding gene and application, and particularly relates to the preparation of gene-targeted drugs for the above-mentioned key genes. The present invention provides the target genes ZIP13 and Transferrin (Tsf) of Parkinson's disease, and significantly alleviates or delays PD by overexpressing ZIP13 or interfering with Tsf by gene silencing. According to the present invention, the target protein of human PD includes the amino acid sequences shown in SEQ ID No. 5 and SEQ ID No. 6, and the gene includes the nucleus as shown in SEQ ID No. 7 and SEQ ID No. 8. nucleotide sequence. According to the target gene of the present invention, constructing an RNAi vector carrying the target gene can be used to improve the exercise ability of PD patients through gene silencing or gene overexpression, and slow down or prevent PD symptoms caused by knockdown of PINK1. This invention is expected to provide new therapeutic strategies and key targets for the treatment of hereditary PD.
Owner:HEFEI UNIV OF TECH
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