Donnerstag, 16. April 2009

Neuronenmusik

Dear Mr. Kopfermann,

Due to your close friendship with my parents from our early childhood, my sister and I both benefited a great deal from being acquainted with you. I am very grateful to my parents that they convinced you to become our music teacher. I can only call it an extraordinary privilege to have had a music teacher of such eminent standing. Unfortunately, the pupil did not quite match the teacher, as I must admit that I could and should have learnt more from you than what I actually did. Yet nevertheless, your teaching had a great impact on me and my conception of what music is, or should be. Above all, the idea that there is a “true” music that must be clearly distinguished from all other kinds of man-made acoustical phenomena. But what is the nature of such “true” music? A person of a far less deep understanding of music like me, might find himself somewhat like Parzival in search of the Holy Grail. What distinguishes “true” music from the rest? While the answer to this question of course resides within the realm of music itself, as a neurobiologist one may see some interesting analogies between how a musical work is composed and neuronal circuits operate.

Naïvely, music can be considered as being comprised of essentially two aspects, i.e. its material (the Töne, which were the famous and hotly-debated subject of so many discussions between you and my father that from my childhood on accompanied me with unfailing intensity over the years) and its arrangement within a composition. Now, in the nervous system we also deal with two such elements, namely (i) the neurons and (ii) their interconnectivity. Neurons may then be seen as analogous to the “Töne” in as much as they occur in different functional flavours. First of all, they may be either excitatory or inhibitory meaning that they may increase or decrease the activity in other neurons to which they are connected. Secondly, they differ in their intrinsic discharge properties, so that some neurons are called “regular spiking” because they discharge their action potentials at regular temporal intervals when stimulated, while others fire in bursts, thus exhibiting an intrinsic dynamic temporal structure in their discharge properties. Finally, the so-called “fast spiking neurons” fire at extremely high frequencies. Within some limits, these features can be considered stable. The particular firing types are due to the equipment with different sets of ion channels that endow these cells with distinct response patterns to the very same stimulus.

While thus considering the neurons as the underlying material from which nervous activity can be composed, the way they are interconnected within the circuitry may be analogous to the composition itself. Due to their specific intrinsic properties, not all possible combinations of connectivity may result in a stable circuit, thereby exerting a selection among all possible combinations. For instance, certain connections may be “prohibited” such as strong feedback excitation that may however occur under pathological conditions such as epilepsy. Here recurrent connections between excitatory neurons result in widespread synchronisation that interferes with the proper functioning of the circuit. In a naïve analogy, such epileptic seizure activity may share some features with synchronisation of musical sound via constant percussion thus disabling a finer temporal dynamic structure.

These considerations about the neurons and their functional assembly may thus be an analogy to the way Töne become assembled in music. Semir Zeki has stated in his book Inner Vision: An exploration of Art and the Brain that in a certain sense painters may be conceived as neurobiologists of vision. Painting would be a process by which we attempt to understand the process of seeing, against a neurological background. He derived this idea from the observation that certain works of art would be tailor-made to optimally activate specific neurons within the path of visual processing. Thus, these paintings may be said to reveal something about the nature of visual processing, as they provide a kind of mirror image of the neuronal circuitry. Likewise, the musician may be seen as a neurobiologist of the acoustical sense and the process of hearing, but possibly also of neuronal processing in a more general way. By means of arranging Töne distinctly combined in a time does he not create a model or mirror image of the temporal structure of neuronal activity?

Remarkably, auditory and visual cortices differ in their micro-architecture. Work from Mriganka-Sur and colleagues revealed that the respective micro-architectures are dependent on “instructions” that the visual and the auditory cortices receive from their corresponding thalamic input structure that relay sensory input [1]. For instance, the redirecting of visual thalamic fibres into the territory of the auditory cortex at certain developmental stages, results in a reorganisation of horizontal connections within this cortical area, hence resembling a visual area. Moreover, animals that underwent such rewiring interpreted the processing of such visual stimuli, even though “perceived” by a piece of auditory cortex, indeed as seeing, not hearing. Thus, in a certain way, the cortex may be thought of as a kind of tabula rasa that can adopt different micro-architectures depending on the temporal structure of the input it receives [2]. This temporal structure may in part be due to some inherent physical properties of the stimuli themselves and will certainly also be dependent on the intrinsic properties of the neuronal elements that are involved in the processing of the stimulus prior to reaching the cortex. But it will also be dependent on the temporal structure of the stimuli upon arrival at the senses. Thus, one may also ask whether some aspects of the cortical micro-architecture may be modifiable by music. A more complex musical composition may also induce a more complex neuronal micro-architecture. If so, one may wonder whether the development of music was accompanied by a development of the brain areas involved in its processing. If so, the term experimental music may gain the additional meaning of experimenting with our own brain.

With this I will finish, not without wishing you all the best for your 70th birthday.

With great affection,
Benedikt Berninger

References:
1. von Melchner, L., Pallas, S.L., and Sur, M. (2000). Visual behaviour mediated by retinal projections directed to the auditory pathway. Nature 404, 871-876.
2. Kalisman, N., Silberberg, G., and Markram, H. (2005). The neocortical microcircuit as a tabula rasa. Proc Natl Acad Sci U S A 102, 880-885.

Samstag, 11. April 2009

http://www.artslant.com/global/artists/show/42326-helmut-berninger

Freitag, 10. April 2009

Voilá the metamorphosis is complete

Socrates’ Error, not yet worked out to perfection...

One of the corner stones of ethics has been the idea of the “Good” as the basis of justification of human behaviour. In the Platonic dialogue “Gorgias” the central question is: What is the nature of the “Good”? The main protagonist of the dialogue, Socrates puts forward that all human action aims at the “Good”. Everything we do because of a “Good” that we believe would result from our doing. When we fail by doing something bad instead, it is not intentionally, but because we did not understand enough well what the real “Good” would be. In fact Socrates challenges the view of his opponent in the dialogue, the Athenian politician Kallicles, who suggests that the “Good” is pleasure.

Socrates believes that knowing the “Good” would also result in doing the “Good”. This statement has been often criticized as against experience. In fact many people seem to know what would be ethically good, yet do not follow its path. Does this disprove Socrates’ view? Taken from a neurobiological point of view, however, we may think that Socrates’ error is not so much his conviction that knowing the good would also mean doing it, but rather consists in his misconception of pleasure. According to modern neurobiology pleasure arises from activation of a neuronal reward system involved in evaluating any given behaviour for its success. Something that Aristotle may have anticipated when he said that every human being aims at understanding and the proof of it resides in the pleasure accompanied even by perception. Ultimately, as a colleague has pointed out to me, we judge even the correctness of our mathematical calculations based on the emotion that arises from finding the solution. Ironically spoken the strength of a proof is measured by the amount of pleasure generated by discovering it.

Now applying this concept of pleasure to behaviour, it seems no more legitimate to dissociate it from the idea of “Good” as Socrates suggested. If we intellectually judge something as “Good”, it is because of the activation of the internal reward system. The dilemma of ethical action does therefore not result from a decision between the “Good” on one hand and pleasure on the other, but between two actions that cause different degrees of pleasure in us. If an unethical action prevails, it is because the brains’ calculation of the anticipated effect results in a greater activation of the reward system. Following the same reasoning, when against the odds a person favours to decide for doing the “Good” it is because his reward system approves this more than a seemingly advantageous but unethical behaviour. Thus, Socrates’ error consists in his misunderstanding of the pivotal role of pleasure in finding the truth.


Epithalamia de Catulo