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倍他司汀

维基百科,自由的百科全书
倍他司汀
臨床資料
商品名Serc, others
AHFS/Drugs.com国际药品名称
懷孕分級
  • C (risk not ruled out)
给药途径口服给药, 鼻腔给药
ATC碼
法律規範狀態
法律規範
  • 处方药(-only)
藥物動力學數據
生物利用度~100%[1]
血漿蛋白結合率<5%[1]
药物代谢肝臟[1]
代謝產物2-(2-Aminoethyl)pyridine英语2-(2-Aminoethyl)pyridine
• 2-Pyridylacetic acid[1]
藥效起始時間英语Onset of action<1 小時 (最大血药浓度)[2]
生物半衰期3.5 小時[3]
排泄途徑尿: 91%[1]
识别信息
  • methyl[2‐(pyridin‐2‐yl)ethyl]amine
CAS号5638-76-6  checkY
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.024.625 編輯維基數據鏈接
化学信息
化学式C8H12N2
摩尔质量136.20 g·mol−1
3D模型(JSmol
  • n1ccccc1CCNC
  • InChI=1S/C8H12N2/c1-9-7-5-8-4-2-3-6-10-8/h2-4,6,9H,5,7H2,1H3 checkY
  • Key:UUQMNUMQCIQDMZ-UHFFFAOYSA-N checkY

倍他司汀INN:betahistine)又称甲胺乙吡啶[4]倍他组啶[5],是组胺H₃受体的拮抗剂反向激动剂,及组胺H₁受体的部分激动剂[6][7][8],可改善内耳血流而發揮作用[9][10],用于治疗眩暈耳鸣(包括美尼尔氏综合症引起的耳鸣)的口服藥物[11]。然而,有關这些適應症的研究证据力薄弱[12][13][14],且可能需要服用數天才會有效[9]

倍他司汀以盐酸倍他司汀(betahistine hydrochloride)、甲磺酸倍他司汀(betahistine mesylate)作为制剂成分,常见副作用包括头痛、恶心和腹部不适[11]。怀孕和哺乳期的安全性不明[11]

倍他司汀于20世纪70年代取得醫療使用許可。雖然它同时也在美国取得使用許可,但随后因疗效有限,而被取消许可,如今此藥仍在其他国家使用[6]。已有學名药流通於市[11]

參見

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参考文獻

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  1. ^ 1.0 1.1 1.2 1.3 1.4 Dickenson A. Drugs in Neurology. Oxford University Press. 2017: 408–409 [2025-01-28]. ISBN 978-0-19-966436-8. (原始内容存档于2024-09-29). 
  2. ^ White R, Bradnam V. Handbook of Drug Administration via Enteral Feeding Tubes 3rd. Pharmaceutical Press. 2015: 125–. ISBN 978-0-85711-162-3. 
  3. ^ Tiziani AP. Havard's Nursing Guide to Drugs. Elsevier Health Sciences. 2013: 1063– [2025-01-28]. ISBN 978-0-7295-8162-2. (原始内容存档于2024-09-29). 
  4. ^ 徐敏,姜丽丽.眩晕和平衡障碍治疗剂——甲胺乙吡啶[J].中国药业, 1999, 8(8):2.DOI:CNKI:SUN:YYGZ.0.1999-08-070.
  5. ^ 芮耀誠. 實用藥物手册. 中華書局. 2002: 225. ISBN 9789622310261. 
  6. ^ 6.0 6.1 Babu, Seilesh; Schutt, Christopher A.; Bojrab, Dennis I. Diagnosis and Treatment of Vestibular Disorders. Springer. 2019: 192 [2020-10-07]. ISBN 978-3-319-97858-1. (原始内容存档于2021-08-28) (英语). 
  7. ^ Hall DA, Wegner I, Smit AL, McFerran D, Stegeman I. Betahistine for tinnitus. Cochrane Database Syst Rev. 2018 Aug 28;2018(8):CD013093. doi: 10.1002/14651858.CD013093. PMCID: PMC6513648.
  8. ^ Poyurovsky M, Pashinian A, Levi A, Weizman R, Weizman A. The effect of betahistine, a histamine H1 receptor agonist/H3 antagonist, on olanzapine-induced weight gain in first-episode schizophrenia patients. Int Clin Psychopharmacol. 2005 Mar;20(2):101-3. doi: 10.1097/00004850-200503000-00007. PMID 15729086.
  9. ^ 9.0 9.1 Adriana P. Tiziani. Havard's Nursing Guide to Drugs. Elsevier Health Sciences. 1 June 2013: 1063– [6 January 2018]. ISBN 978-0-7295-8162-2. (原始内容存档于28 August 2021). Adriana P. Tiziani (1 June 2013). Havard's Nursing Guide to Drugs. Elsevier Health Sciences. pp. 1063–. ISBN 978-0-7295-8162-2. Archived from the original on 28 August 2021. Retrieved 6 January 2018.
  10. ^ Murdin L, Hussain K, Schilder AG. Betahistine for symptoms of vertigo. Cochrane Database Syst Rev. 2016 Jun 21;2016(6):CD010696. doi: 10.1002/14651858.CD010696.pub2. PMID 27327415; PMCID: PMC7388750.
  11. ^ 11.0 11.1 11.2 11.3 BNF 79 : March 2020.. London: Royal Pharmaceutical Society. 2020: 453. ISBN 9780857113658. 
  12. ^ Murdin, L; Hussain, K; Schilder, AG. Betahistine for symptoms of vertigo.. The Cochrane database of systematic reviews. 21 June 2016, (6): CD010696. PMID 27327415. doi:10.1002/14651858.CD010696.pub2. 
  13. ^ Wegner, I; Hall, DA; Smit, AL; McFerran, D; Stegeman, I. Betahistine for tinnitus.. The Cochrane database of systematic reviews. 28 December 2018, 12: CD013093. PMID 30908589. doi:10.1002/14651858.CD013093.pub2. 
  14. ^ James, AL; Burton, MJ. Betahistine for Menière's disease or syndrome.. The Cochrane database of systematic reviews. 2001, (1): CD001873. PMID 11279734. doi:10.1002/14651858.CD001873.