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Objective and quantitative measures to assess the severity and progression of Huntington's disease (HD) are desirable. Several studies have demonstrated quantifiable deficits in the coordination of precision grasping in patients with Huntington's disease. Correlation analysis revealed that the amount of grip force variability while holding an object was correlated to the total motor score of the Unified Huntington's Disease Rating Scale (UHDRS) in a cross-sectional study. In addition, grip force variability increased in all HD patients during a 3-year follow-up. The UHDRS total motor score did not change significantly in the same subjects. The results suggest that neurophysiological analysis of isometric grip forces may detect disease progression more sensitively than clinical rating scales. The applicability of the assessment of grip forces in clinical studies is currently tested in large multicenter studies. Possible applications of the technique as a biomarker in clinical studies in HD are discussed.
Introduction
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder with a prevalence of about 7–10 symptomatic patients per 100,000 individuals and about double the number of pre-symptomatic gene carriers (Harper, 1996). Expansion of a CAG-repeat within exon 1 of the HD gene results in the development of the HD phenotype (The Huntington's Disease Collaborative Research Group, 1993), with longer repeats associated with earlier manifestation and faster progression of disease (Andrew et al., 1993).
The development of skilled hand movements such as grasping and object manipulation is of fundamental importance to the ability to perform everyday life activities. The purpose of this chapter is to provide an overview on development of grasping and object manipulation. The first part describes developmental characteristics of prehension, i.e. reaching and grasping. The second part deals with the development of independent finger movements, which is an important prerequisite for both grip formation and object manipulation. In the third part, aspects of manipulation of unstable and stable objects are discussed. This includes discussion of the development of sensory control mechanisms, i.e. adaptation to friction and weight of the manipulated object. Finally, the concept of neuronal group selection, a concept that implies that development is the result of complex interaction between genes and environment, is described.
Introduction
Prehension (i.e. reaching and grasping) and manipulation of objects are motor skills that are fundamentally important for exploration and interaction with the environment. Although human infants can grasp from an early age, it takes several years before children are able to perform these skills in a mature pattern. The development of these skilled hand movements and underlying neural mechanisms is the focus of this chapter.
Prehension involves two main components, i.e. reaching and grasping. First, the hand has to be moved to the location of the object. Second, the grip must be adapted to size, shape, orientation and the intended use of the object (see also Chapters 1 and 12).
This chapter underlines the multifaceted nature of reach and grasp behavior by reviewing several computational models that focus on selected features of reach-to-grasp movements. An abstract meta-model is proposed that subsumes previous modeling efforts, and points towards the need to develop computational models that embrace all the facets of reaching and grasping behavior.
Introduction
Hand transport and hand (pre)shaping are basic components of primate grasping. The different views on their dependence and coordination lead to different explanations of human control of grasping. One can view these two components as being controlled independently but coordinated so as to achieve a secure grasp. The alternative view is that the hand and the arm are taken as a single limb and controlled using a single control mechanism. Needless to say, this distinction is not very sharp; but it becomes a choice to be made by a control engineer when it is necessary to actually implement a grasp controller. The experimental findings so far point towards the view that human grasping involves independent but coordinated control of the arm and the hand (see Jeannerod et al., 1998) (see also Chapter 10). However, reports against this view do exist as it has been suggested that human grasping is a generalized reaching movement that involves movement of digits so as to bring the fingers to their targets on the object surface (Smeets & Brenner, 1999, 2001). Although theoretically both control mechanisms are viable, from a computational viewpoint, the former is more likely.
Stroke results in irreversible brain damage, with the type and severity of symptoms dependent upon the location and the amount of injured brain tissue. The most common neurological impairment caused by stroke is partial weakness, called paresis, reflecting a reduced ability to voluntarily activate spinal motoneurons. In conjunction with the general reduced ability to voluntarily activate spinal motoneurons, there is often a reduced ability to selectively activate the spinal motoneuron pools, i.e. turning on some neurons while not turning on others. Together, these mechanisms result in altered movement control of many muscles, especially the contralesional hand and arm muscles used for grasping. Because of the altered muscle control, a variety of kinematic and kinetic alterations are observed during grasping in people with paresis post stroke. Impairments in grasping are related to the inability to use the hand for functional activities during daily life. In rare instances, stroke affects the posterior parietal lobe, resulting in distinct grasping deficits that are substantially different from grasping deficits seen after corticospinal system damage. Future studies investigating grasping post stroke could include the examination of both kinematic and kinetic aspects of grasping in the same subject samples, the examination of different types of grasping (e.g. palmar, precision), and the examination of different time points post stroke.
General information about stroke
Stroke is an acute neurological event that is caused by an alteration in blood flow to the brain.
Our knowledge about an object small enough to be grasped with the hand usually begins first with a visual appreciation of its size and shape. However, in the dark or when searching a deep pocket or purse, vision is impossible. Consequently a haptic exploration procedure is the only course of action and scanning an object's surface with the fingertips provides information about friction, shape, compliance, temperature and friction that is unattainable by visual inspection. This initial information is of particular importance to subsequent object manipulation and dexterous handling. Both exploratory hand movements and object manipulation make efficient use of specialized low-threshold mechanoreceptors in the skin which are selectively sensitive to both normal and tangential (shearing) forces as well as slip on the skin. This cutaneous feedback guides the exploratory movements and provides a signal of when a tactile target is encountered. These primary afferent signals are subsequently transformed by cell assemblies in the somatosensory cortex to generate central representations or internal models of the object's salient physical features. Neuronal signals encoding the internal model of shape, friction and center of mass are then relayed directly by cortico-cortical projections from the somatosensory cortex to motor cortex. The subsequent dexterous object manipulation is driven by anticipatory motor control strategies based on the internal model of the object's features which are used to direct grip forces and finger positions.
Dopaminergic medication or deep brain stimulation of the subthalamic nucleus (STN DBS) impact on many aspects of the grip–lift task in idiopathic Parkinson's disease (PD). The rate of both grip- and load-force generation were normalized by the levodopa test, whereas the maximum vertical acceleration was not improved in all studies. Other dopa-responsive factors included load preparation time, which was shortened, and maximal grip force that showed an extra increase in the test. The overflow of grip force and maximum negative load force was correlated with the intensity of levodopa-induced dyskinesias (LID) in patients affected by this symptom. Maximal negative load force and tremor were not dopa-sensitive. Subthalamic nucleus DBS exerted a dopa-like effect on most parameters of the grip–lift task except for grip force in the long-term comparison. In patients with LID the preoperative overflow of force in on-state and the severity of LID were both ameliorated by STN-DBS, although the force level did not return to normal values in all studies. A dopa-resistant action tremor of higher frequency can be seen during the grip–lift task, while the rest tremor of PD is suppressed at onset of the movement. Further therapies involve facilitation of movements with a training augmented by external cues like auditory or visual signals to overcome akinesia. The grip–lift task offers a valuable instrument to study therapeutic effects in PD.
Introduction
Dopaminergic medication or deep brain stimulation of the subthalamic nucleus impact on almost any aspect of motor deficits in idiopathic Parkinson's disease (PD).
Vertebrate myelin membranes are compacted and held in close apposition by three structural proteins of myelin, myelin basic protein, myelin protein zero (MPZ) and myelin proteolipid protein (PLP1/DMalpha). PLP1/DMalpha is considered to function as a scaffolding protein and play a role in intracellular trafficking in oligodendrocytes. In humans, point mutations, duplications or deletions of PLP1 are associated with Pelizaeus–Merzbacher disease and spastic paraplegia Type 2. PLP1 is highly conserved between mammals, but less so in lower vertebrates. This has led some researchers to question whether certain fish species express PLP1 orthologues at all, and to suggest that the function of PLP1/DMalpha in the central nervous system (CNS) may have been taken over by MPZ. Here, we review the evidence for the conservation of orthologues of PLP1/DMalpha in actinopterygian fishes and provide a comparison of currently available sequence data across 17 fish species. Our analysis demonstrates that orthologues of PLP1/DMalpha have been retained and are functionally expressed in many, if not all, extant species of bony fish. Many of the amino acids that, when mutated, are associated with severe CNS pathology are conserved in teleosts, demonstrating conservation of essential functions and justifying the development of novel disease models in species such as the zebrafish.
An individual's autobiographical memory is made up of their episodic memory, memory for specific episodes of their lives, and their conceptual, generic, and schematic knowledge of their personal history: their autobiographical knowledge. In a typical act of remembering, these two types are brought together and a specific memory from one's life is recalled. These autobiographical memories are the content of the self. They locate us in sociohistorical time, they locate us in our societies and in our social groups, they define the self. In important ways, autobiographical memories allow the self to develop and at the same time they constrain what we can become. In this chapter we outline a little of what is known about the representation of autobiographical memories in the mind and how they are constructed in consciousness. With this in mind, we then turn to the function that autobiographical memories have in defining the self by making certain networks of memories that ground the self in making a specific experienced reality highly accessible.
AN INTRODUCTION TO AUTOBIOGRAPHICAL MEMORY RESEARCH
Although the formal scientific study of memory has been in existence for at least a century, since the early work of scientists such as Ebbinghaus (1885/1964), Galton (1883), and Ribot (1882), the study of autobiographical memory was neglected during much of this period as a result of the complexities associated with this type of recall.
After the attacks on the World Trade Center and Pentagon on September 11, 2001, the Princeton historian Bernard Lewis explained the thinking and behavior of Muslims to the American public in a New Yorker article (Lewis, 2001). Lewis wrote that, unlike Americans, Muslims know and care about history:
In current American usage, the phrase “that's history” is commonly used to dismiss something as unimportant, of no relevance to current concerns. … Middle Easterner's perception of history is nourished from the pulpit, by the schools, and by the media, and although it may be – indeed, often is – slanted and inaccurate, it is nevertheless vivid and powerfully resonant. (p. 51)
Lewis implies that Americans' (and presumably most Westerners') historical memories are not “nourished from the pulpit, by the schools, and by the media.” He further implies that Americans' historical memories are accurate, even if they do not care much about history.
In this chapter, we dispute each of these claims. Muslims are not unique in their use or abuse of history. People's memories of the histories of the national, ethnic, or religious groups to which they belong (ingroups) are often tilted in favor of their ingroups and against other groups. We present evidence that historical memories are skewed, in part, because children and adults are presented with selective and biased depictions of the past. Educators, religious leaders, politicians, and media all play an important role by influencing the knowledge available.
Culture is no explanation – that much is (or should be) obvious to all social scientists. Saying that people do this or believe that “because that's their culture” is at most a descriptive statement – telling us that the behavior or belief in question is widespread in the particular group we are considering – but it begs the question: Why are those behaviors or beliefs common in that group?
Surprisingly, this is a rather new interest in the social sciences. Chiefly responsible for this odd lack of interest was the perennial reluctance of many social scientists to consider micro-processes and their aggregation – that is, the way that individual processes and behaviors create large-scale social phenomena (Schelling, 1978). However, in the last twenty years, a new anthropology and psychology of cultural transmission has emerged, founded on the systematic study of micro-processes – the field has its theoretical foundations (Boyd & Richerson, 1985; Sperber, 1985; Tooby & Cosmides, 1992), its mathematical formalisms (McElreath & Boyd, 2007), and droves of empirical studies (see e.g., Atran, 1990; Boyer, 1994; Hirschfeld, 1996 and many others). The main thrust in most of these studies is the study of particular cognitive dispositions and their consequences for cultural transmission, a domain that Pascal Boyer surveys in the final chapter of this book.
One of the ancestors of this field is Milman Parry, who as a young classicist in the 1930s proposed an original (and to many scholars scandalous) explanation of Homeric formulae, these recurrent pairs of nouns and epithets (“rose-fingered Dawn,” “fleet-footed Achilles,” “heifer-eyed Aphrodite,” “Apollo, rouser of armies,” etc.
Memory is as the affection: we remember the things which we love and the things which we hate.
Ralph Waldo Emerson
Almost nothing renders us human as much as our unique capacity for memory. Other animals surely have memory in biological and even social forms. They can do amazing things in flocks and herds. But no other creatures can use memory to create, to record experience, to forge self-conscious associations, to form and practice language, to know, collect, narrate, and write their pasts. We not only can know at least some of our past; we know that we can know it. Sometimes it seems that memory really is the root, the fountain of human intelligence. It is this deeply human power of memory that makes it so ubiquitous, so essential to human life, but also such a problem and such a subject of inquiry. As the Israeli philosopher Avishai Margalit has written: “Memory is knowledge from the past. It is not necessarily knowledge about the past” (Margalit, 2004). In everyday life, and in the world of scholarship (whether cognitive psychology, neuroscience, anthropology, literature, or history), all considerations of memory seem perpetually to ride on the teeter-totter of trust and distrust, up and down, with distrust carrying the most weight, and trust struggling to keep the teeter-totter moving at all. Can we believe what memory provides us? Can we afford not to?
This chapter is about the cultural memory and transmission of oral traditions, especially those that use poetics and music. The latter include many of the best studied and most stable forms of oral traditions, including children rhymes, ballads, songs, and epic poetry. Oral traditions are of interest because, unlike written traditions, they depend primarily on memory for their survival. Thus, by examining the products of long periods of oral transmission, we can learn something about the processes of memory used. Working in the other direction, by using our knowledge of memory, we can better understand how the products came into being and what their likely limitations are. Although they are often viewed only as art forms in current times, oral traditions did, and often still do, transmit valuable practical and moral information and in many forms, such as the epics sung in the Balkans, give insight into major conflicts (Foley, 1991; Havelock, 1978; Lord, 1960; Ong, 1982).
In large part, this chapter is drawn from my earlier work on oral traditions (e.g., Rubin, 1995), but here I intend to show how it provides a more general view of memory as used in the cultural transmission of information. My goal is to show that current theories of memory need to be expanded in principled and theoretically well-supported ways if they are going to be maximally useful in helping us understand individual and collective memory.
The field of history is premised on the idea that knowledge of our past can inform our behaviors in the future. Indeed, this idea is central to many assumptions within personality, developmental, and clinical psychology. Implicit in this thinking is that history is somehow made up of immutable facts that are set in stone in society's memory. Who, after all, could doubt the accuracy of America's role in World War II, the facts surrounding the discovery of the New World by Columbus in 1492, the bravery and upstanding characters of the men who defended the Alamo in 1845, or the profound effect of the Magna Carta in 1215? These events, of course, are not as straightforward as we were taught in grade school. Events such as these undergo rethinking, reinterpreting, and even forgetting to become part of the permanent fabric of collective memory. But the transition from cultural upheaval to history does not happen all at once. The macrocosm of how a collective memory is built over centuries takes place on a much smaller scale beginning in the days, weeks, and months following an event.
The purpose of this chapter is to suggest that our current psychological state shapes our thinking about historical events in the same way that historical events shape our current thinking. Just as the key to the future may be the past, the key to the past may be the present. What about an event that makes it memorable?
We call those concepts and norms that seem to be shared within a group and differ from those of other groups “cultural.” We call concepts and norms “cultural” if people have them because other people in their group have them or had them before. This suggests that transmission of concepts and norms is at the heart of what constitutes human cultures.
To what extent does cultural transmission require memory? The answer of modern cognitive anthropology is slightly surprising. If we understand “memory” in the ordinary sense of information about past situations that we can access and consider explicitly, the answer is that cultural transmission does not actually require as much of that kind of memory as we would generally assume. Indeed, a great deal of cultural transmission takes place outside of explicit memories, as I explain here. But memory, for psychologists, includes more than just explicit memories (Roediger, Wheeler, & Rajaram, 1993). It comprises systematic information about the social and natural environment, what is called “semantic memory,” as well as the many skills and habits known as “procedural memory.” Once we understand memory, as psychologists do, as including all these processes beyond conscious inspection (Roediger, 1990), then memory really is the crux of cultural transmission. In the pages that follow, I will justify these statements on the basis of a few examples of cultural domains where the work of memory (in the wider sense) has been extensively studied.
Where were you when you first heard about the 9/11 attacks? Do you remember what you were doing at the time? How did you feel when you first heard the news, and how does thinking about this event make you feel now? As of this writing, many Americans over the age of 15 most likely find these questions remarkably easy to answer. The fact that a singular event in history could be remembered so well, and by so many people, is relevant to at least two lines of research in the memory literature.
First, the very fact that people can answer such questions so easily is relevant to research and theory on “flashbulb memories” (Brown & Kulik, 1977; Kvavilashvili, Mirani, Schlagman, & Kornbrot, 2004; Sharot, Martorella, Delgado, & Phelps, 2006). As originally conceptualized, flashbulb memories were regarded as extraordinarily detailed, long-lasting, and unusually accurate “snapshots” of the specific context in which an unexpected, emotion-laden event occurred (Brown & Kulik, 1977). Over the years, research has qualified some of the early claims regarding such memories. For example, even though people often perceive that such memories are accurate, such recollections can contain the same sorts of distortions one finds with other types of memories (Neisser & Harsch, 1992). Nevertheless, more recent work has found that flashbulb memories can sometimes be extraordinarily accurate and detailed, provided that the event has direct, personal relevance to the perceiver (Bernsten & Thomsen, 2005).