کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5847915 1561612 2015 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Acetylcholinesterase activity of electric eel is increased or decreased by selected monoterpenoids and phenylpropanoids in a concentration-dependent manner
ترجمه فارسی عنوان
فعالیت استیل کولین استراز قارچ الکتریکی توسط مونوترپنیدهای انتخاب شده و فنیل پروپانوئید ها به روش وابسته به غلظت افزایش یا کاهش می یابد
کلمات کلیدی
فعال سازی استیل کولین استراز، بیماری آلزایمر، تعاونی تعاونی، روغن ضروری،
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
چکیده انگلیسی


- Micro molar monoterpenoid rises and mmolar monoterpenoid lowers Torpedo AChE activity.
- The Hill number for AChE inhibition by some monoterpenoids ranges 1.6-2.0.
- The Hill number shows that two monoterpenoid molecules can bind with AChE.
- The above point explains synergism/antagonism of mixed monoterpenoids on AChE.

The profitable insecticidal action of monoterpenoids prompted us to test their efficiency against stored-grain beetle species, via inhibition of acetylcholinesterase (AChE). For this, we first studied the ability of the monoterpenoids geraniol, linalool, camphor, fenchone, carvone and γ-terpinene, besides the phenylpropanoids trans-anethole and estragole to inhibit Electrophorus AChE. The results indicated that while AChE activity increased (15-35%) with 40 μM geraniol, camphor, γ-terpinene and linalool, the activity decreased (60-40%) with 5 mM carvone, γ-terpinene, and fenchone. The Km for AChE was 0.52 ± 0.02 mM in control assays, which fell to 0.28 ± 0.01 mM or 0.32 ± 0.01 mM in assays with 20 μM linalool or γ-terpinene added. In the millimolar range, the terpenoids behaved as weak inhibitors. Unexpectedly, AChE inhibition by camphor, carvone, γ-terpinene, and fenchone gave Hill numbers ranging 2.04-1.57, supporting the idea that AChE was able to lodge more than one monoterpenoid molecule. The plots of 1/v vs. 1/S at varying monoterpenoid provided straight lines, fenchone and γ-terpinene acting as competitive inhibitors and carvone and camphor as non-competitive inhibitors. Moreover, the secondary plots of the slope KMapp/Vmaxapp vs. [I] and of 1/Vmaxapp vs. [I] gave parabolic curves, which lent support to the proposed capacity of AChE to bind more than one monoterpenoid molecule. The fitting of the curves to a second-order polynomial equation allowed us to calculate the inhibition constants for the interaction of AChE with fenchone, γ-terpinene, carvone and camphor. The previously unnoticed increase in AChE activity with monoterpenoids should be considered as a reminder when advising the use of essential oils of plants or their constituents as anti-AChE agents to attenuate pathological signs of Alzheimer's disease.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemico-Biological Interactions - Volume 229, 5 March 2015, Pages 36-43
نویسندگان
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