Treatment of pancreatitis using alpha 7 receptor-binding cholinergic agonists
    1.
    发明申请
    Treatment of pancreatitis using alpha 7 receptor-binding cholinergic agonists 有权
    使用α7受体结合胆碱能激动剂治疗胰腺炎

    公开(公告)号:US20090123456A1

    公开(公告)日:2009-05-14

    申请号:US11724605

    申请日:2007-03-15

    摘要: A method of treating a patient suffering from pancreatitis comprising treating said patient with a therapeutically effective amount of a cholinergic agonist selective for an α7 nicotinic receptor in an amount sufficient to decrease the amount of the proinflammatory cytokine that is released from a macrophage wherein said condition is acute pancreatitis. The compounds of the present invention include a quaternary analog of cocaine; (1-aza-bicyclo[2.2.2]oct-3-yl)-carbamic acid 1-(2-fluorophenyl)-ethyl ester; a compound of formula (I), a compound of formula (II), a compound of formula (III), a compound of formula (IV), and an oligonucleotide or mimetic capable of attenuating the symptoms of acute pancreatitis wherein the oligonucleotide or mimetic consists essentially of a sequence greater than 5 nucleotides long that is complementary to an mRNA of an α7 cholinergic receptor. The variables of formulae (I), (II), (III) and (IV) are described herein.

    摘要翻译: 一种治疗患有胰腺炎的患者的方法,其包括以足以减少从巨噬细胞释放的促炎细胞因子的量的治疗有效量的对α7烟碱受体选择性的胆碱能激动剂治疗所述患者,其中所述病症是 急性胰腺炎。 本发明的化合物包括可卡因的四元类似物; (1-氮杂 - 双环[2.2.2]辛-3-基) - 氨基甲酸1-(2-氟苯基) - 乙酯; 式(I)化合物,式(II)化合物,式(III)化合物,式(IV)化合物和能够减弱急性胰腺炎症状的寡核苷酸或模拟物,其中寡核苷酸或模拟物 基本上由大于5个核苷酸长的序列组成,其与α7胆碱能受体的mRNA互补。 本文描述了式(I),(II),(III)和(IV)的变量。

    Treatment of inflammation using α7 receptor-binding cholinergic agonists
    3.
    发明授权
    Treatment of inflammation using α7 receptor-binding cholinergic agonists 有权
    使用α7受体结合胆碱能激动剂治疗炎症

    公开(公告)号:US07785808B2

    公开(公告)日:2010-08-31

    申请号:US11724605

    申请日:2007-03-15

    IPC分类号: G01N33/567 G01N33/53

    摘要: A method of treating a patient suffering from pancreatitis comprising treating said patient with a therapeutically effective amount of a cholinergic agonist selective for an α7 nicotinic receptor in an amount sufficient to decrease the amount of the proinflammatory cytokine that is released from a macrophage wherein said condition is acute pancreatitis. The compounds of the present invention include a quaternary analog of cocaine; (1-aza-bicyclo[2.2.2]oct-3-yl)-carbamic acid 1-(2-fluorophenyl)-ethyl ester; a compound of formula (I), a compound of formula (II), a compound of formula (III), a compound of formula (IV), and an oligonucleotide or mimetic capable of attenuating the symptoms of acute pancreatitis wherein the oligonucleotide or mimetic consists essentially of a sequence greater than 5 nucleotides long that is complementary to an mRNA of an α7 cholinergic receptor. The variables of formulae (I), (II), (III) and (IV) are described herein.

    摘要翻译: 一种治疗患有胰腺炎的患者的方法,其包括以足以减少从巨噬细胞释放的促炎细胞因子的量的治疗有效量的对α7烟碱受体选择性的胆碱能激动剂治疗所述患者,其中所述病症是 急性胰腺炎。 本发明的化合物包括可卡因的四元类似物; (1-氮杂 - 双环[2.2.2]辛-3-基) - 氨基甲酸1-(2-氟苯基) - 乙酯; 式(I)化合物,式(II)化合物,式(III)化合物,式(IV)化合物和能够减弱急性胰腺炎症状的寡核苷酸或模拟物,其中寡核苷酸或模拟物 基本上由大于5个核苷酸长的序列组成,它与α7胆碱能受体的mRNA互补。 本文描述了式(I),(II),(III)和(IV)的变量。

    TREATMENT OF INFLAMMATION USING ALPHA 7 RECEPTOR-BINDING CHOLINERGIC AGONISTS
    4.
    发明申请
    TREATMENT OF INFLAMMATION USING ALPHA 7 RECEPTOR-BINDING CHOLINERGIC AGONISTS 审中-公开
    使用ALPHA治疗炎症7受体结合胆碱酯酸激酶

    公开(公告)号:US20100256341A1

    公开(公告)日:2010-10-07

    申请号:US12818347

    申请日:2010-06-18

    IPC分类号: C07K16/00

    摘要: A method of treating a patient suffering from pancreatitis comprising treating said patient with a therapeutically effective amount of a cholinergic agonist selective for an α7 nicotinic receptor in an amount sufficient to decrease the amount of the proinflammatory cytokine that is released from a macrophage wherein said condition is acute pancreatitis. The compounds of the present invention include a quaternary analog of cocaine; (1-aza-bicyclo[2.2.2]oct-3-yl)-carbamic acid 1-(2-fluorophenyl)-ethyl ester; a compound of formula (I), a compound of formula (II), a compound of formula (III), a compound of formula (IV), and an oligonucleotide or mimetic capable of attenuating the symptoms of acute pancreatitis wherein the oligonucleotide or mimetic consists essentially of a sequence greater than 5 nucleotides long that is complementary to an mRNA of an α7 cholinergic receptor. The variables of formulae (I), (II), (III) and (IV) are described herein.

    摘要翻译: 一种治疗患有胰腺炎的患者的方法,其包括以足以减少从巨噬细胞释放的促炎细胞因子的量的治疗有效量的对α7烟碱受体选择性的胆碱能激动剂治疗所述患者,其中所述病症是 急性胰腺炎。 本发明的化合物包括可卡因的四元类似物; (1-氮杂 - 双环[2.2.2]辛-3-基) - 氨基甲酸1-(2-氟苯基) - 乙酯; 式(I)化合物,式(II)化合物,式(III)化合物,式(IV)化合物和能够减弱急性胰腺炎症状的寡核苷酸或模拟物,其中寡核苷酸或模拟物 基本上由大于5个核苷酸长的序列组成,它与α7胆碱能受体的mRNA互补。 本文描述了式(I),(II),(III)和(IV)的变量。

    TREATMENT OF INFLAMMATION USING ALPHA 7 RECEPTOR-BINDING CHOLINERGIC AGONISTS
    5.
    发明申请
    TREATMENT OF INFLAMMATION USING ALPHA 7 RECEPTOR-BINDING CHOLINERGIC AGONISTS 审中-公开
    使用ALPHA治疗炎症7受体结合胆碱酯酸激酶

    公开(公告)号:US20110166148A1

    公开(公告)日:2011-07-07

    申请号:US12724888

    申请日:2010-03-16

    摘要: A method of treating a patient suffering from pancreatitis comprising treating said patient with a therapeutically effective amount of a cholinergic agonist selective for an α7 nicotinic receptor in an amount sufficient to decrease the amount of the proinflammatory cytokine that is released from a macrophage wherein said condition is acute pancreatitis. The compounds of the present invention include a quaternary analog of cocaine; (1-aza-bicyclo[2.2.2]oct-3-yl)-carbamic acid 1-(2-fluorophenyl)-ethyl ester; a compound of formula (I), a compound of formula (II), a compound of formula (III), a compound of formula (IV), and an oligonucleotide or mimetic capable of attenuating the symptoms of acute pancreatitis wherein the oligonucleotide or mimetic consists essentially of a sequence greater than 5 nucleotides long that is complementary to an mRNA of an α7 cholinergic receptor. The variables of formulae (I), (II), (III) and (IV) are described herein.

    摘要翻译: 一种治疗患有胰腺炎的患者的方法,其包括以足以减少从巨噬细胞释放的促炎细胞因子的量的治疗有效量的对α7烟碱受体选择性的胆碱能激动剂治疗所述患者,其中所述病症是 急性胰腺炎。 本发明的化合物包括可卡因的四元类似物; (1-氮杂 - 双环[2.2.2]辛-3-基) - 氨基甲酸1-(2-氟苯基) - 乙酯; 式(I)化合物,式(II)化合物,式(III)化合物,式(IV)化合物和能够减弱急性胰腺炎症状的寡核苷酸或模拟物,其中寡核苷酸或模拟物 基本上由大于5个核苷酸长的序列组成,它与α7胆碱能受体的mRNA互补。 本文描述了式(I),(II),(III)和(IV)的变量。

    Treatment of pancreatitis using alpha 7 receptor-binding cholinergic agonists
    6.
    发明授权
    Treatment of pancreatitis using alpha 7 receptor-binding cholinergic agonists 有权
    使用α7受体结合胆碱能激动剂治疗胰腺炎

    公开(公告)号:US07238715B2

    公开(公告)日:2007-07-03

    申请号:US10957426

    申请日:2004-09-30

    IPC分类号: A01N43/40

    摘要: A method of treating a patient suffering from pancreatitis comprising treating said patient with a therapeutically effective amount of a cholinergic agonist selective for an α7 nicotinic receptor in an amount sufficient to decrease the amount of the proinflammatory cytokine that is released from a macrophage wherein said condition is acute pancreatitis. The compounds of the present invention include a quaternary analog of cocaine; (1-aza-bicyclo[2.2.2]oct-3-yl)-carbamic acid 1-(2-fluorophenyl)-ethyl ester; a compound of formula (I), a compound of formula (II), a compound of formula (III), a compound of formula (IV), and an oligonucleotide or mimetic capable of attenuating the symptoms of acute pancreatitis wherein the oligonucleotide or mimetic consists essentially of a sequence greater than 5 nucleotides long that is complementary to an mRNA of an α7 cholinergic receptor. The variables of formulae (I), (II), (III) and (IV) are described herein

    摘要翻译: 一种治疗患有胰腺炎的患者的方法,其包括以足以减少从巨噬细胞释放的促炎细胞因子的量的治疗有效量的对α7烟碱受体选择性的胆碱能激动剂治疗所述患者,其中所述病症是 急性胰腺炎。 本发明的化合物包括可卡因的四元类似物; (1-氮杂 - 双环[2.2.2]辛-3-基) - 氨基甲酸1-(2-氟苯基) - 乙酯; 式(I)化合物,式(II)化合物,式(III)化合物,式(IV)化合物和能够减弱急性胰腺炎症状的寡核苷酸或模拟物,其中寡核苷酸或模拟物 基本上由大于5个核苷酸长的序列组成,其与α7胆碱能受体的mRNA互补。 本文描述了式(I),(II),(III)和(IV)的变量

    Method for avoiding handover failure

    公开(公告)号:US10420166B2

    公开(公告)日:2019-09-17

    申请号:US13542247

    申请日:2012-07-05

    IPC分类号: H04W76/30 H04W8/08 H04W36/00

    摘要: Methods for avoiding handover failure are provided. The method includes determining, by a source Base Station (BS), to perform a handover of a User Equipment (UE); determining, by the source BS, whether a target BS connects with a user plane node serving the UE at the source BS; and releasing resources, when the target BS does not connect with the user plane node serving the UE at the source BS.

    Method for detachment of MS moving between communication systems

    公开(公告)号:US09867157B2

    公开(公告)日:2018-01-09

    申请号:US12527328

    申请日:2008-02-13

    IPC分类号: H04W60/06 H04W76/06

    CPC分类号: H04W60/06 H04W76/32

    摘要: A method for detachment of a mobile set within the equivalent route area moving between the communication systems comprising steps of: during the detachment process is implemented between a mobile set and a service node in one communication system, the service node generates one or more messages and transmits it to the service nodes in one or more communication system within the ERA. If the message is transmitted to the service node within the ERA of only one communication system, this service node transmits this message or the message generated according to this message to the service nodes within the ERA of the other communication system. With the method proposed in present invention, when a mobile is detached from two or more communication systems which share the same ERA, the service nodes in all communication systems within the ERA can still correctly manage the relevant information on this mobile set.