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M Hurry

Publications and source records attributed to M Hurry.

2 recordsLinked to original sources

Short-term total sleep deprivations does not selectively impair higher cortical functioning.

Previous research has shown that total sleep deprivation produces impairment in sustained attention and vigilance especially if the deprivation period is greater than 48 hours. However little is known about the effects of sleep deprivation on performance of tasks considered to be measures of higher cortical functioning such as tests of cognitive flexibility and the capacity to shift from one response set to another. One current hypothesis is that sleep deprivation of a shorter duration (34-36 hours) adversely affects higher cortical function while effects on attention and vigilance tasks are relatively mild. Performance on an intelligence test, a test of sustained attention and tests designed to measure higher cortical function were compared in a group of 29 subjects who underwent 34-36 hours of continuous sleep deprivation and 32 normal sleeping control subjects. No significant group performance differences in the hypothesized direction were noted on any measure. One night of total sleep deprivation does not appear to impair performance on tasks that are designed to assess higher cortical functioning.

Adult↗

The antinociceptive and motivational effects of intranigral injection of opioid agonists.

The antinociceptive potency of morphine and the morphine metabolite morphine-6-glucuronide (M6G) was examined after injection into the substantia nigra and periaqueductal gray (PAG) of rats. Both drugs produced antinociception in both sites. The antinociceptive potency of M6G was significantly greater than morphine in the nigra. There was no difference in the antinociceptive potency of M6G in the nigra and PAG. M6G and other opioids were also examined for motivational effects after intranigral injection. A high dose of intranigral morphine (10.0 nmol) produced a conditioned place preference. No significant motivational effects were produced by 1.0 nmol of M6G, D-Ala2, N-Me-Phe4,Gly5-ol-enkephalin (DAGO), D-Pen2,D-Pen5-enkephalin (DPDPE), or U-50,488H. It is concluded that the substantia nigra plays an important role in opioid antinociception. The role of the nigra in opioid reward is questionable.

3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cycloh↗