کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5503963 1400207 2016 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Apomorphine therapy in Parkinson's disease and future directions
ترجمه فارسی عنوان
درمان آپومورفین در بیماری پارکینسون و جهت های آینده
کلمات کلیدی
آپومورفین، بیماری پارکینسون، غیر دهانی، آینده،
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی سالمندی
چکیده انگلیسی


- In future apomorphine buccal thin film or inhalation could become rescue therapy for off periods in Parkinson's disease.
- A cutaneous patch pump therapy may be an alternative to needle based subcutaneous therapy.
- An oral option using an ester may be a feasible therapy in future. Animal model studies look promising.
- Apomorphine may have an anti-amyloid deposition effect in the brain.

Apomorphine infusion or injection is an important dopamine agonist non-oral therapy usually used in advanced Parkinson's disease (PD) with refractory motor fluctuations. The drug also has appreciable efficacy for nonmotor fluctuations and is the quickest to reverse predictable “off” periods. Current subcutaneous administration, however, is complicated by problems associated with needle-based therapies, such as skin nodule formation, skin irritation, and avoidance of this treatment option by needle-phobic subjects.In this review we focus on what the future might hold for apomorphine injection/infusion. We discuss interesting and novel delivery strategies of apomorphine or esters via oral, buccal, inhalation and a novel pump-patch route. We also discuss recent research that has highlighted some important properties of apomorphine in animal models, such as a potential anti-amyloid effect and its potential impact in the management of PD dementia or perhaps even Alzheimer's disease. A potential role for apomorphine infusion in cases with impulse control disorders and other nonmotor issues is also discussed.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Parkinsonism & Related Disorders - Volume 33, Supplement 1, December 2016, Pages S56-S60
نویسندگان
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