کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5738862 1615061 2017 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Research articleInhibiting medial septal cholinergic neurons with DREADD alleviated anxiety-like behaviors in mice
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
Research articleInhibiting medial septal cholinergic neurons with DREADD alleviated anxiety-like behaviors in mice
چکیده انگلیسی


- We investigated the role of medial septal cholinergic neurons in anxiety-like behaviors with DREADD.
- Temporal inhibition of medial septal cholinergic neurons produced consistent anxiolytic effects in three behavioral models.
- Temporal inhibition of medial septal cholinergic neurons increased voluntary exploration in the open field test.
- These results reconciled conflicting findings from previous studies using irreversible lesions or non-specific inhibition.

Cholinergic neurons in the medial septum (MS) participate in a variety of cognitive and emotional behaviors. Some studies but not others show that lesions or inhibition of the MS reduce anxiety-like behaviors and locomotive exploration in rats. However, these conclusions come from manipulations that are either irreversible or non-specific to cholinergic neurons, casting doubt on their validity. With DREADD (designer receptors exclusively activated by designer drugs), we temporarily and reversibly inhibited cholinergic neurons in the MS. We observed consistent anxiolytic effects of MS cholinergic inhibition in the novelty-suppressed feeding test, the marble burying test and the elevated plus-maze test, as well as increased exploratory activities in the open field test. These findings confirm an excitatory role of the MS cholinergic neurons in the control of innate anxiety, and reconcile conflicting findings from previous studies using irreversible lesions or non-specific inhibition.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience Letters - Volume 638, 18 January 2017, Pages 139-144
نویسندگان
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