Elzbieta Jankowska

Bio: Elzbieta Jankowska is an academic researcher from University of Gothenburg. The author has contributed to research in topics: Spinal cord & Inhibitory postsynaptic potential. The author has an hindex of 64, co-authored 204 publications receiving 14343 citations. Previous affiliations of Elzbieta Jankowska include Tokyo Medical and Dental University & Nencki Institute of Experimental Biology.

The Effect of DOPA on the Spinal Cord 6. Half‐centre organization of interneurones transmitting effects from the flexor reflex afferents

Abstract: JANKOWSKA, E., M. G. M. JUKES, S. LUND and A. LUNDBERG. The effect of DOPA on the spinal cord. 6. Half- centre organization of interneurones transmitting effects from theyexor rejex aferents. Acta physiol. scand. 1967. 70. 389-402. In unanaesthetized spinal cats a systematic microelectrode exploration has been made in the lumbosacral spinal cord in order to find interneurones that may transmit the late longlasting reflex effects that volleys in the FRA (flexor reflex afferents) evoke after an intravenous injection of DOPA. Interneurones that may transmit these late effects are found in the lateral part of Rexed’s layer VII and three main types are identified: A) cells activated from the ipsilateral FRA and inhibited from the contralateral FRA, B) cells activated from the contralateral FRA and inhibited from the ipsilateral FRA, C) cells activated from both the ipsilateral and contralateral FRA. The receptive fields and other criteria employed suggest that type A and B transmit excitatory action to flexor and extensor motoneurones respectively, and type C depolatization to Ia afferent terminals. The functional organization of these pathways is discussed mainly in relation to the mechanisms responsible for the long latency and duration of the discharge.

The Effect of DOPA on the Spinal Cord 5. Reciprocal organization of pathways transmitting excitatory action to alpha motoneurones of flexors and extensors

Abstract: In unanaesthetized spinal cats, injected with L-DOPA, volleys in the flexor reflex afferents (FRA) evoke a long-latency, longlasting discharge in ipsilateral flexor and contralateral extensor motoneurones. It is postulated that this discharge is transmitted by a neuronal pathway which is inhibited in the normal acute spinal cat, presumably from the pathway, which in this state transmits the shortlatency effect from the FRA to motoneurones. The organization of the pathway released by an injection of DOPA has been analyzed by recording the discharges in efferents to flexors and extensors and with intracellular records from motoneurones. Combined stimulation of ipsilateral and contralateral FRA reveals a reciprocal organization in that either flexor or extensor motoneurones are activated. Transmission from the ipsilateral FRA to flexor motoneurones can be inhibited by volleys in the contralateral FRA, and transmissiqn from the contralateral FRA to extensor motoneurones by volleys in the ipsilateral FRA. These inhibitory effects are neither produced postsynaptically in the motoneurones nor presynaptically by depolarization of primary afferents and are hence exerted at an interneuronal level. The organization of reciprocal innervation at an interneuronal level is discussed in relation to the primary afferent depolarization evoked in Ia afferent terminals after DOPA and to rhythmic alternating movements.

An electrophysiological demonstration of the axonal projections of single spinal interneurones in the cat

Abstract: 1. Single interneurones excited from group Ia afferents and located in the ventral horn of the spinal cord in the cat were activated antidromically by stimulation of their axons with one micro-electrode while recording extracellularly close to their somas with a second micro-electrode. The interneurones studied were those which, according to previous indirect evidence, should mediate the reciprocal Ia inhibition of motoneurones.2. Two subgroups of these interneurones were studied: those excited from group Ia afferents in the quadriceps (Q) and posterior bicepssemitendinosus (PBSt) nerves. Most of them could be activated from a number of separate loci in the PBSt and Q motor nuclei respectively and from the ventral or lateral funiculi.3. The location of the axonal branches and the extent of their branching in the motor nuclei were reconstructed by comparing the latencies of the responses and the thresholds (0.1-5 muA) for antidromic activation of single interneurones from different electrode positions in a number of tracks, having previously established the relation between the threshold and the distance from the stimulated fibres. For the main branches in the white matter the conduction velocity was found to be about 70 m/sec.4. The axonal projections of the investigated interneurones were found to be fully consistent with the hypothesis that they mediate reciprocal inhibition of motoneurones.

The rubrospinal tract. II. Facilitation of interneuronal transmission in reflex paths to motoneurones

Abstract: Summary. 1. The effect of stimulation of the red nucleus on transmission of synaptie actions from different systems of primary afferents to alpha motoneurones has been invest/gated in cats, mainly with intracellular recording from motoneurones. 2. The dominating effect is facilitation, presumably caused by excitatory action exerted from the rubrospinal tract on interneurones of reflex arcs. The time course of facilitation suggests that the minimal linkage from the rubrospinal tract to these interneurones is monosynaptic. 3. Interneuronal transmission in reflex pathways from the following afferent systems is facilitated : a) Ia inhibitory between flexors and extensors, l~ubrospina] facilitation did not reveal Ia inhibitory pathways between adductors and abductors at the hip. b) Ib excitatory and inhibitory. There is marked facilitation of the reciprocal effects evoked by Ib afferents from extensors but also of other Ib pathways, for example inhibitory from extensors to flexor nuclei and from flexors to extensor nuclei and excitatory from flexors to extensor nuclei, e) Low threshold joint, inhibitory and excitatory, presumably from afferents with Ruffini endings. d) Low threshold cutaneous, excitatory and inhibitory. Since transmission from these afferents could be facilitated under conditions when there was no effect on transmission from high threshold muscle afferents it is postulated that the effect is exerted on pathways which are not part of the common pathways from the flexor reflex afferents, e) Flexor reflex afferents, excitatory and inhibitory. Facilitation of these pathways is not found regularly, in some eases there was no effect and in others inhibition. 4. The effeets are discussed in relation to the complex effects evoked from the rnbro spinal tract in motoneurones and to supraspinal regulation of proprioceptive reflexes. 5. It is postulated that in complex movements alternative Ib patterns may be mobilized, whereas flexion-extension movements are subserved by the Ib pattern found in the spinal eat. 6. Facilitation of the Ia inhibitory pathway is taken to indicate "a-y-linkage" in reciprocal inhibition. It is pointed out that convergence from Ia and descending impulses on a common inhibitory interneurone may play an important role in the regulation of a-y-linked flexion-extension movements.

Sources of input to interneurones mediating group I non-reciprocal inhibition of motoneurones in the cat.

Abstract: Intracellular recordings have been made from laminae V-VI interneurones interposed in pathways of non-reciprocal inhibition of motoneurones from group I afferents of triceps surae and/or plantaris. A comparison of actions of brief stretches of triceps surae and plantaris with actions of electrical stimulation of nerves of these muscles revealed that I a afferents influenced about a half of the interneurones excited by I b afferents. Electrical stimulation of seven muscles nerves, three cutaneous nerves, posterior knee joint and interosseous nerves, the red nucleus and the pyramidal tract, evoked excitatory post-synaptic potentials (e.p.s.p.s) in various proportions of interneurones. Most of the interneurones were excited monosynaptically, or both monosynaptically and disynaptically by group I afferents. This, together with a very small proportion of interneurones in which e.p.s.p.s were evoked only disynaptically, indicates that the same last-order interneurones may subserve di- and trisynaptically evoked inhibition of motoneurones. Other fibre systems excited these interneurones monosynaptically (interosseal, rubro- and corticospinal), disynaptically (cutaneous, rubro- and corticospinal) and polysynaptically. The coupling of the earliest e.p.s.p.s from group II and joint afferents could not be established, but was consistent with their mediation by only one or two interposed interneurones. Inhibition was evoked from all fibre systems with excitatory input to the same or to other interneurones of the sample, except from group II afferents, the effects of which were found in a much smaller number of cells and may not be fully representative.

The synaptic organization of the brain

Abstract: Introduction to synaptic circuits, Gordon M.Shepherd and Christof Koch membrane properties and neurotransmitter actions, David A.McCormick peripheral ganglia, Paul R.Adams and Christof Koch spinal cord - ventral horn, Robert E.Burke olfactory bulb, Gordon M.Shepherd, and Charles A.Greer retina, Peter Sterling cerebellum, Rodolfo R.Llinas and Kerry D.Walton thalamus, S.Murray Sherman and Christof Koch basal ganglia, Charles J.Wilson olfactory cortex, Lewis B.Haberly hippocampus, Thomas H.Brown and Anthony M.Zador neocortex, Rodney J.Douglas and Kevan A.C.Martin Gordon M.Shepherd. Appendix: Dendretic electrotonus and synaptic integration.

Spinal and Supraspinal Factors in Human Muscle Fatigue

Abstract: Muscle fatigue is an exercise-induced reduction in maximal voluntary muscle force. It may arise not only because of peripheral changes at the level of the muscle, but also because the central nervous system fails to drive the motoneurons adequately. Evidence for “central” fatigue and the neural mechanisms underlying it are reviewed, together with its terminology and the methods used to reveal it. Much data suggest that voluntary activation of human motoneurons and muscle fibers is suboptimal and thus maximal voluntary force is commonly less than true maximal force. Hence, maximal voluntary strength can often be below true maximal muscle force. The technique of twitch interpolation has helped to reveal the changes in drive to motoneurons during fatigue. Voluntary activation usually diminishes during maximal voluntary isometric tasks, that is central fatigue develops, and motor unit firing rates decline. Transcranial magnetic stimulation over the motor cortex during fatiguing exercise has revealed focal cha...

Neuroscience 細胞死：最近の知見

Abstract: 中枢神経系疾患の治療は正常細胞（ニューロン）の機能維持を目的とするが，脳血管障害のように機能障害の原因が細胞の死滅に基づくことは多い．一方，脳腫瘍の治療においては薬物療法や放射線療法といった腫瘍細胞の死滅を目標とするものが大きな位置を占める．いずれの場合にも，細胞死の機序を理解することは各種病態や治療法の理解のうえで重要である．現在のところ最も研究の進んでいる細胞死の型はアポトーシスである．そのなかで重要な位置を占めるミトコンドリアにおける反応および抗アポトーシス因子について概要を紹介する．