Ho, Tsz Wan. / Thesis (Ph.D.)--Chinese University of Hong Kong, 2009. / Includes bibliographical references (leaves 125-165). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstract also in Chinese.

Thesis (M.S.)--State University of New York at Binghamton, Department of Psychology, 2009. / Includes bibliographical references.

There are numerous clinical and experimental accounts of retrograde and anterograde amnesia resulting from damage to the hippocampus (HPC). Several theories on the HPC hold that only certain types of recent memories should be affected by HPC damage. These theories do not accurately predict the circumstances within which memories are vulnerable to HPC damage. Here I show the HPC plays a role in the formation and storage of a wider range of memories than is posited in contemporary theories. I will demonstrate that an important factor in elciting retrograde amnesia is the number of similar learning episodes. Exposure to multiple problems in the same task context leads to retorgrade amnesia that is not observed when only one problem is learned under otherwise identical parameters. When multiple discriminations are learned, the output of the HPC blocks recall from and future use of the extra-HPC memory system. / x, 78 leaves : ill. ; 29 cm.

Long-term adrenalectomy (ADX) results in a specific loss of dentate gyrus granule cells in the hippocampus of adult rats, occurring over a period of weeks to months. This loss of granule cells results in cognitive deficits in a number of tasks that depend on intact hippocampal function. The gradual nature of ADX-induced cell death and the ensuing deficits in cognition are similar to those experienced by patient populations suffering from a variety of pathological conditions. Here we present an animal model by which we use ADX to produce a loss of granule cells within the hippocampus of rats. We also provide experimental evidence for a treatment strategy by which the lost granule cells may be replaced, with the goal of functional recovery in mind. / xii, 191 leaves : ill. (chiefly col.) ; 28 cm

The thesis examines the ability of animals to construct a home base. The home base is a point in space where animals rear, groom, and circle and is a primary element in organized spatial behaviour (Eilam and Golani 1989). Once animals establish a home base, they make outward trips and stops, and after a series of trips and stops they return again to the home base. The home base behaviour of animals acts as a platform for asking questions about the cognitive organization of an environment. The thesis describes five main findings. Control and hippocampectomized animals use (1) proximal and (2) distal cues to form a home base and organize their behaviour. (3) Control and olfactory bulbectomized animals form home bases in the dark where as hippocampectomized animals are impaired suggesting self-movement but not olfactory cues play a role in home base behaviour. A final set of experiments demonstrated that control and hippocampectomized animals learn the position of (4) proximal and (5) distal cues so that in the cue's absence, animals still form a home base at that position. The demonstration that a central feature of exploratory behaviour, establishing a home base, is preserved in hippocampectomized rats in relation to proximal, distal, and conditioned visual cues - reveals that exploratory behaviour remains organized after hippocampal lesions. The inability of hippocampectomized rats to form a virtual home base in the absence of visual cues is discussed in relation to the idea that the hippocampus contributes to inertial behaviour that may be dependent upon self-movement cues. / xv, 232 leaves : ill. ; 29 cm.

The behavioural and electrophysiological consequences of two newly developed aniracetam analogues were investigated in male Long-Evans rats. Results indicate that an intraperitoneal (i.p.) injection of LD38.2 significantly improved retention in a two odour olfactory discrimination task. However, three different dosages of LN1 did not facilitate memory in the task. In rats with chronically implanted electrodes, both compounds rapidly crossed the blood brain barrier (BBB) after an i.p. injection and influenced several parameters of the field excitatory postsynaptic potential (EPSP) in the CA1 and dentate gyrus regions of the hippocampus. The enhancement of the field EPSP following LD38.2 administration may be related to the drug's ability to facilitate memory in the olfactory discrimination task. Compounds, like LD38.2, that enhance both hippocampal transmission and performance in learning/memory tasks in laboratory rodents may have implications for the treatment of clinical memory disorders.

The hippocampus is necessary for normal memory in rodents, birds, monkeys, and people. Damage to the hippocampus can result in the inability to learn new facts, defined by the relationship among stimuli. In rodents, spatial learning involves learning about the relationships among stimuli, and exemplifies the kind of learning the requires the hippocampus. Therefore, understanding the neural mechanisms underlying spatial learning may elucidate basic memory processes. Many hippocampal neurons fire when behaving rats, cats, or monkeys are in circumscribed regions (place fields) of an environment. The neurons, called place cells, fire in relation to distal stimuli, but can persist in signaling location when the stimuli are removed or lights are turned off (memory fields). In this thesis, computational models of spatial information processing simulated many of the defining properties of hippocampal place cells, including memory fields. Furthermore, the models suggested a neurally plausible mechanism of goal directed spatial navigation which involved the encoding of distances in the connections between place cells. To navigate using memory fields, the models required an excitatory, distributed, and plastic association system among place cells. Such properties are well characterized in area CA3 of the hippocampus. In this thesis, a new electrophysiological study provides evidence that a second system in the dentate gyrus has similar properties. Thus, two circuits in the hippocampus meet the requirements of the models. Some predictions of the models were then tested in a single-unit recording experiment in behaving rats. Place fields were more likely to occur in information rich areas of the environment, and removal of single cues altered place fields in a way consistent with the distance encoding mechanism suggested by the models. It was concluded that a distance encoding theory of rat spatial navigation has much descriptive and predictive utility, but most of its predic

Activity-induced immediate-early gene (IEG) transcription foci can be labelled with fluorescent probes, permitting high temporal and spatial resolution in mapping neuronal circuits. Previous quantification approaches have assumed a Boolean function of transcription foci, assuming that cells are either active or inactive. Due to multiple amplification steps in the in situ hybridization process, it was thought that information relating to magnitudes of firing rates was lost. However, the current data suggest that transcription foci actually exhibit non-Boolean intensity and size values which vary according to behavioural condition. Systematic characterization of transcription foci intensity and size revealed incremental variations such that: home-cage < one-environment exposure < five-environment exposure < maximal electroconvulsive shock. Visual differences in transcription foci may result from a quantifiable relationship between spiking patterns and transcription rates. The exact stoichiometry between neuronal spiking and transcription is not yet clear, but these results suggest that Boolean applications of IEG imaging may neglect accurate neuronal activation properties. / xvi, 125 leaves : ill. ; 29 cm

Adrenalectomy (ADX) has been shown to cause selective degeneration of granule cells in the dentate gyrus (DG). This occurs due to the reduction of corticosterone (CORT) and behavioural deficits are associated with the loss of these neurons. Dentate lesions and cell loss associated with ADX have been shown to effect behaviour in a number of spatial tasks. In contras, it has been shown granule cell loss does not affect the specificity of place cells in CA3 and CA1. We used the ADX model to examine the role of DG granule cells plays in representing space using immediate early gene (IEG) activation in the principal hippocampal subfields after exploration of novel environments. Rats were allowed to free explore multiple novel environments and then the mRNA for the IEG Homer 1a (H1a) was used as a marker of neural activity. After degeneration of approximately half of the DG granule cells we found a significant increase in number of active cells in the DG, CA3 and CA1 in ADX animals. The results indicate a reduction in granule cells causes a dramatic increase in the proportion of remaining DG granule cells in response to exploration. The change in DG activation disrupts the representations in CA3 and CA1 and thereby affects behaviour. / vii, 60 leaves : ill. (some col.) ; 29 cm

Thesis (M.S.)--University of Michigan, 1993.