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Dopamine

Daga Wikipedia, Insakulofidiya ta kyauta.
Dopamine
type of chemical entity (en) Fassara
Bayanai
Ƙaramin ɓangare na catecholamine (en) Fassara da phenethylamine alkaloid (en) Fassara
Amfani magani
Stylized name (en) Fassara DOPamine
Sinadaran dabara C₈H₁₁NO₂
Canonical SMILES (en) Fassara C1=CC(=C(C=C1CCN)O)O
Medical condition treated (en) Fassara kidney disease (en) Fassara, bradycardia (en) Fassara da neurogenic shock (en) Fassara
Contributing factor of (en) Fassara decision making (en) Fassara
Significant drug interaction (en) Fassara phenelzine (en) Fassara, linezolid (en) Fassara, phenelzine (en) Fassara, phenelzine (en) Fassara da phenelzine (en) Fassara
Manufacturer (en) Fassara Pfizer (mul) Fassara
Produced by (en) Fassara Dopaminergic cell groups (en) Fassara

Dopamine, wanda ake siyarwa a ƙarƙashin sunan Intropin da sauransu, magani ne da aka fi amfani da shi wajen magance matsin jini, jinkirin bugun zuciya wanda ke haifar da alamomi, kuma, idan ba a samun epinephrine ba, dakatarwar zuciya.[1] A cikin jarirai da aka haifa ya ci gaba da zama magani da aka fi so don ƙarancin hawan jini.[2] A cikin yara ana fi son epinephrine ko norepinephrine yayin da a cikin manya ana fi son norepinefrine don ƙananan hawan jini.[3][4] Ana ba da shi ta hanyar jijiyan jini ko intraosseously a matsayin ci gaba da ruwa.[1] Tasirin yawanci yakan fara ne a cikin minti biyar.[1] Ana ƙara yawan su don yin tasiri.[1]

Sakamakon cututtuka na yau da kullun sun haɗa da kara aikin koda, bugun zuciya mara kyau, ciwon kirji, amai, ciwon kai, ko damuwa.[1] Idan ya shiga cikin nama mai laushi a kusa da jijiya gida mutuwa na iya faruwa.[1] Ana iya ba da maganin phentolamine don ƙoƙarin rage wannan haɗarin.[1] Ba a san ko dopamine yana da aminci don amfani da shi a lokacin daukar ciki ko shayarwa ba.[1] A ƙananan allurai dopamine galibi yana haifar da Masu karɓar dopamine da masu karɓa na β1-adrenergic yayin da a manyan allurai yana aiki ta hanyar Masu karɓar α-adrenergic.[1]

An fara hada Dopamine a cikin dakin gwaje-gwaje a cikin 1910 ta hanyar George Barger da James Ewens a Ingila.[5] Yana cikin Jerin Magunguna Masu Muhimmanci na Hukumar Lafiya ta Duniya.[6] Kudin da aka kashe a kasashe masu tasowa na akwati na 400mg yana tsakanin $ 0.28 da $ 0.60 (USD) tun daga shekarar 2014.[7]  A cikin ilimin lissafin ɗan adam Neurotransmitter)" id="mwcw" rel="mw:WikiLink" title="Dopamine (neurotransmitter)">dopamine ne neurotransmitter da kuma hormone.

Bayanan da aka ambata

[gyara sashe | gyara masomin]
  1. 1 2 3 4 5 6 7 8 9 "Dopamine Hydrochloride". drugs.com. American Society of Health-System Pharmacists. June 29, 2016. Archived from the original on 14 September 2016. Retrieved 15 July 2016.
  2. Bhayat, SI; Gowda, HM; Eisenhut, M (8 May 2016). "Should dopamine be the first line inotrope in the treatment of neonatal hypotension? Review of the evidence". World Journal of Clinical Pediatrics. 5 (2): 212–22. doi:10.5409/wjcp.v5.i2.212. PMC 4857235. PMID 27170932.
  3. De Backer, D; Aldecoa, C; Njimi, H; Vincent, JL (March 2012). "Dopamine versus norepinephrine in the treatment of septic shock: a meta-analysis*". Critical Care Medicine. 40 (3): 725–30. doi:10.1097/ccm.0b013e31823778ee. PMID 22036860.
  4. Dellinger, RP; Levy, MM; Rhodes, A; Annane, D; Gerlach, H; Opal, SM; Sevransky, JE; Sprung, CL; Douglas, IS; Jaeschke, R; Osborn, TM; Nunnally, ME; Townsend, SR; Reinhart, K; Kleinpell, RM (February 2013). "Surviving sepsis campaign: international guidelines for management of severe sepsis and septic shock: 2012". Critical Care Medicine. 41 (2): 580–637. doi:10.1097/CCM.0b013e31827e83af. PMID 23353941.
  5. Fahn S (2008). "The history of dopamine and levodopa in the treatment of Parkinson's disease". Movement Disorders. 23 Suppl 3: S497–508. doi:10.1002/mds.22028. PMID 18781671. According to Hornykiewicz,6 dopamine was first synthesized by George Barger and James Ewens in 1910 at the Wellcome labs in London, England.
  6. Empty citation (help)
  7. "Dopamine". International Drug Price Indicator Guide. Archived from the original on 22 January 2018. Retrieved 5 December 2015.