نتایج جستجو برای: licking
تعداد نتایج: 1178 فیلتر نتایج به سال:
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Drinking was induced in food-deprived rats by a fixed-time 1-min schedule of food presentation. With three rats, d-amphetamine (0.25, 0.5, 1.0, and 2.0 mg/kg) led to a dose-related increase in licking early in the interfood intervals, the peak of the temporal distribution of licking being shifted to earlier values. These effects were seen even when d-amphetamine had no effect on overall rates o...
The pattern of licking microstructure during various phases of a conditioned taste aversion (CTA) was evaluated. In Experiment 1, rats ingested lithium chloride (LiCl) for 3 trials and were then offered sodium chloride (NaCl) or sucrose on 3 trials. A CTA to LiCl developed and generalized to NaCl but not to sucrose. CTA intake suppression was characterized by reductions in burst size, average i...
An emerging literature suggests that the medial prefrontal cortex (mPFC) is crucial for the ability to track behavioral outcomes over time and has a critical role in successful foraging. Here, we examine this issue by analyzing changes in neuronal spike activity and local field potentials in the rat mPFC in relation to the consumption of rewarding stimuli. Using multi-electrode recording method...
Injections of the melanocortin 3/4 receptor (MCR) agonist melanotan II (MTII) to a variety of brain structures produces anorexia, suggesting distributed brain MCR control of food intake. We performed a detailed analysis of feeding behavior (licking microstructure analysis) after a range of MTII doses (0.005 nM to 1 nM) was targeted to the forebrain (third ventricle, 3V) or hindbrain (fourth ven...
Rats were required to complete varying numbers of licks (FR), ranging from 10 to 300, in order to free an activity wheel for predetermined times (CT) ranging from 2 to 20 sec. The reinforcement of drinking by running was shown both by an increased frequency of licking, and by changes in length of the burst of licking relative to operant-level burst length. In log-log coordinates, instrumental l...
Licking patterns and molarity preferences, elicited by two sets of sucrose solutions (0.0 to 1.75 M and 1.0 to 3.0 M), were measured in six young and six aged squirrel monkeys. Sucrose preference thresholds were determined for each age group using sucrose concentrations from 0.025 to 0.1 M. Age was unrelated to sucrose preference thresholds. Consummatory activity of all monkeys increased monoto...
سابقه و هدف: نیکوتین اثرات فارماکولوژیک گسترده ای در سیستم عصبی مرکزی و محیطی دارد. رفتار لیسیدین Licking در موش صحرایی عمدتا با عملکرد هسته های دم دار و جسم سیاه مرتبط است. هدف این مطالعه تعیین مکانیسم اثر نیکوتین در این رفتار می باشد. مواد و روش ها: حیوانات مورد آزمایش، موش های صحرایی نژاد آلبینو به وزن تقریبی 250-150 گرم بوده که بطور جداگانه در قفس نگهداری می شدند. تعداد لیسیدین در مدت 60 دق...
Neurons that fire in relation to licking, in the ventral part of the dorsolateral striatum (DLS), were studied during acquisition and performance of a licking task in rats for 14 sessions (2 h/d). Task learning was indicated by fewer errors of omission of licking and improved movement efficiency (i.e., shorter lick duration) over sessions. Number of licks did not change over sessions. Overtrain...
Despite decades of study, it remains a matter of controversy as to whether in rats taste identification is a rapid process that occurs in about 250-600 ms (one to three licks) or a slow process that evolves over seconds. To address this issue, we trained rats to perform a taste-cued two-response discrimination task (2-RDT). It was found that, after learning, regardless of intensity, the deliver...
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