1
MOTIVATION The cerebellum is involved in controlling and learning smooth coordinated movements, therefore an accurate understanding of how this control engine works should have a strong impact on the control of biomorphic robots. ŸWe have studied the possible control implications that the inferior olivedeep cerebellar nuclei cell connections (IODCN) may present in a distributed-synaptic- plasticity cerebellar model (activity conveyed by this connection seems to control plasticity at DCN synapses (Bengtsson & Hesslow 2006) (Ruigrok & Voogd 2000)). ŸThe Marr and Albus model hypothesized that parallel fibers (PFs) presented LTP/ LTD synaptic mechanisms so as to correlate the activity at PFs with an error signal through climbing fibers. In subsequent studies it has been demonstrated that most of the cerebellar connections show traces of plasticity (Hansel, Linden & DAngelo 2001). ŸWe have developed a firing-rate cerebellar model (Garrido et al. 2012) with plasticity mechanisms at PFPC and at DCN synaptic inputs (from Mossy Fibers (MFs), Purkinje Cells (PCs) and IO). Therefore, we present a model where the IODCN pathway plays a fundamental role by refining the cerebellar learning performance. CONCLUSIONS he results suggest that the cerebellar gain control is a consequence of the MFDCN and PCDCN Tsynaptic plasticity working in balance with IODCN connection. Thus, this balance (homeostasis), which is implemented through different learning, enhances the cerebellar learning performance. IODCN connection ensures stability in the very early learning stages, that is, while the weights of MFDCN and PCDCN connections have yet to stabilize. Once the learning process is finished, the IODCN connection effect ceases. ACKNOWLEDGMENTS: This work was supported in part by the EU project REALNET (IST-270434). THE POSSIBLE CONTROL IMPLICATIONS OF THE INFERIOR OLIVE DEEP CEREBELLAR NUCLEI PATHWAY IN A DISTRIBUTED PLASTICITY CEREBELLAR MODEL 2 3 Jesús A. Garrido ,Richard R. Carrillo , 2 Consorzio Interuniversitario per le Scienze Fisiche della Materia (CNISM), Pavia, Italy; 1 1 Niceto R. Luque , Eduardo Ros , 1 3 Dept. Computer Architecture and Technology, University of Granada, Spain; Dept. of Computer Architecture and Electronics, University of Almeria, Spain. CEREBELLAR MODEL ur cerebellar model includes the following plasticity mechanisms: O IO-driven LTD and LTP at PFPC connections. IO-driven LTP and LTD at PCDCN connections. PC-driven LTD and LTP at MFDCN connections. PC-driven LTD and LTP at PCDCN connections. . FURTHER INFORMATION: If you are interested in this work or any other related information from our group, please do not hesitate to contact me at [email protected]. DIFFERENT CONTROL PATHWAYS DURING LEARNING PROCESS Figure 2. Effect of the presented plasticity mechanisms. A. The feedforward control loop trough IODCN ensures stability during the first stage of the learning process. B. The distributed learning process through different pathways ensures a relatively fast synaptic weight adjustment by using the PFPC plasticity mechanism and the subsequent slow adaptation of the excitation and inhibition levels by means of the MFDCN and PCDCN synaptic plasticity mechanisms. These mechanisms also helps keep the PFPC synaptic weight values in their optimum range (in our experiments, this range has been fixed to [0, 1], although other ranges could be suitable). Figure 4. Comparison between the MAE evolution with/without using IO-DCN connection when manipulating different masses (2.5kg, 6kg, 10kg). The system gain has been set to manipulate up to 0.5kg. The manipulated masses are larger than expected, so the existing plasticity mechanisms at MF/PCDCN adjust the cerebellar output to cope with these masses. The model with IODCN connection supplies a proper adjustment from the beginning of the learning process ( A ) ? Figure 1. Cerebellar microcircuitry, main components of the cerebellar paths and plasticity sites included. The cerebellum receives proprioceptive signals through MFs. These inputs follow two different pathways: the first one reaches the DCN through the cerebellar cortex, and the second one contacts directly the DCN cells. Long-term plasticity has been represented using two colors: red indicates potentiation (LTP) and blue indicates depression (LTD). CONTROL ARCHITECTURE he adaptive cerebellar module delivers corrective add-on torque values to compensate for deviations in the inverse Tdynamic module when manipulating an object of mismatched weight Figure 3. Light-Weight-Robot (LWR) simulator within a feed- forward control loop. The robot-plant physical characteristics can be modified to match different contexts (different contexts means that the object manipulated by the robot (payload) has different weights). This LWR robot is a 7-DOF arm composed of revolute joints. We used the first, second and fifth joint maintaining the others fixed. RESULTS he plasticity mechanisms that determine the synaptic strength in were driven by the activity from PCs which is responsible for the balance (homeostasis) between all these plasticity laws. This PC Tactivity makes MFDCN and PCDCN synaptic strength increase while makes the IODCN synaptic strength decrease. During the first learning stages the IODCN corrective action predominates (Fig5.C and 5.D).Afterwards, this corrective action is gradually decreased while the corrective action provided by MFDCN and PCDCN connections is gradually increased. The transition between these two control actions is regulated by the PC activity which in turn, is working in a constant range of frequencies thanks to MFDCN and PCDCN connections. We obtain a system able to self-adapt by means of a distributed learning where all the learning sites are complementary working together. MFDCN/PCDCN/IODCN connections Figure 5. Synaptic weight evolution during the learning process, at IODCN, MFDCN and PCDCN connections when using a 10kg payload and initial parameters for a 0.5 kg payload setting. (A) Synaptic weight at MFDCN. (B) Synaptic weight at PCDCN. (C) Normalized synaptic weight at IODCN. (D) Synaptic weight at IODCN. ( B ) 0 0.5 1 -0.1 -0.05 0 0.05 0.1 0.15 0.2 0.25 0.3 JOINT POSITIONS (rad) JOINT POSITIONS -0.1 0 0.1 0 0.5 1 0.538 0.54 0.542 0.544 0.546 Y(m) CARTESIAN POSITIONS Z(m) q1 q2 q3 Benchmark Trajectory to be accomplished

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Page 1: Omechanisms: Ttorque values to compensate for deviations ...nluque/PostersResumenActividadInvestigadora/post_A0xedu4.pdfMOTIVATION The cerebellum is involved in controlling and learning

MOTIVATION

The cerebellum is involved in controlling and learning smooth coordinated movements, therefore an accurate understanding of how this control engine works should have a strong impact on the control of biomorphic robots.ŸWe have studied the possible control implications that

the inferior olive→ deep cerebellar nuclei cell connections (IO→ DCN) may present in a distributed-synaptic-plasticity cerebellar model (activity conveyed by this connection seems to control plasticity at DCN synapses (Bengtsson & Hesslow 2006) (Ruigrok & Voogd 2000)).

ŸThe Marr and Albus model hypothesized that parallel fibers (PFs) presented LTP/ LTD synaptic mechanisms so as to correlate the activity at PFs with an error signal through climbing fibers. In subsequent studies it has been demonstrated that most of the cerebellar connections show traces of plasticity (Hansel, Linden & DAngelo 2001).

ŸWe have developed a firing-rate cerebellar model (Garrido et al. 2012) with plasticity mechanisms at PF→

PC and at DCN synaptic inputs (from Mossy Fibers (MFs), Purkinje Cells (PCs) and IO). Therefore, we present a model where the IO→ DCN pathway plays a fundamental role by refining the cerebellar learning performance.

.

CONCLUSIONS

he results suggest that the cerebellar gain control is a consequence of the MF→ DCN and PC→ DCN Tsynaptic plasticity working in balance with IO→DCN

connection. Thus, this balance (homeostasis), which is implemented through different learning, enhances the cerebellar learning performance. IO→ DCN connection ensures stability in the very early learning stages, that is, while the weights of MF→ DCN and PC→ DCN connections have yet to stabilize. Once the learning process is finished, the IO→DCN connection effect ceases.

ACKNOWLEDGMENTS: This work was supported in part by the EU project REALNET (IST-270434).

THE POSSIBLE CONTROL IMPLICATIONS OF THE INFERIOR OLIVE DEEP CEREBELLAR NUCLEI PATHWAY IN A DISTRIBUTED PLASTICITY CEREBELLAR MODEL

2 3Jesús A. Garrido ,Richard R. Carrillo , 2Consorzio Interuniversitario per le Scienze Fisiche della Materia (CNISM), Pavia, Italy;

1 1 Niceto R. Luque , Eduardo Ros ,1 3 Dept. Computer Architecture and Technology, University of Granada, Spain; Dept. of Computer Architecture and Electronics, University of

Almeria, Spain.

CEREBELLAR MODEL

ur cerebellar model includes the following plasticity mechanisms:O

IO-driven LTD and LTP at PF→PC connections.IO-driven LTP and LTD at PC→ DCN connections.PC-driven LTD and LTP at MF→DCN connections.PC-driven LTD and LTP at PC→DCN connections..

FURTHER INFORMATION: If you are interested in this work or any other related information from our group, please do not hesitate to contact me at [email protected].

DIFFERENT CONTROL PATHWAYS DURING LEARNING PROCESS

Figure 2. Effect of the presented plasticity mechanisms.A. The feedforward control loop trough IO→DCN ensures stability during the first stage of the learning process.B. The distributed learning process through different pathways ensures a relatively fast synaptic weight adjustment by using the PF→PC plasticity mechanism and the subsequent slow adaptation of the excitation and inhibition levels by means of the MF→DCN and PC→DCN synaptic plasticity mechanisms. These mechanisms also helps keep the PF→ PC synaptic weight values in their optimum range (in our experiments, this range has been fixed to [0, 1], although other ranges could be suitable).

Figure 4. Comparison between the MAE evolution with/without using IO-DCN connection when manipulating different masses (2.5kg, 6kg, 10kg). The system gain has been set to manipulate up to 0.5kg. The manipulated masses are larger than expected, so the existing plasticity mechanisms at MF/PC→DCN adjust the cerebellar output to cope with these masses. The model with IO→ DCN connection supplies a proper adjustment from the beginning of the learning process( A )

?

Figure 1. Cerebellar microcircuitry, main components of the cerebellar paths and plasticity sites included. The cerebellum receives proprioceptive signals through MFs. These inputs follow two different pathways: the first one reaches the DCN through the cerebellar cortex, and the second one contacts directly the DCN cells. Long-term plasticity has been represented using two colors: red indicates potentiation (LTP) and blue indicates depression (LTD).

CONTROL ARCHITECTURE

he adaptive cerebellar module delivers corrective add-on torque values to compensate for deviations in the inverse Tdynamic module when manipulating an object of

mismatched weight

Figure 3. Light-Weight-Robot (LWR) simulator within a feed-forward control loop. The robot-plant physical characteristics can be modified to match different contexts (different contexts means that the object manipulated by the robot (payload) has different weights). This LWR robot is a 7-DOF arm composed of revolute joints. We used the first, second and fifth joint maintaining the others fixed.

RESULTS

he plasticity mechanisms that determine the synaptic strength in were driven by the activity from PCs which is responsible for the balance (homeostasis) between all these plasticity laws. This PC Tactivity makes MF→ DCN and PC→ DCN synaptic strength increase while makes the IO→ DCN synaptic strength

decrease. During the first learning stages the IO→ DCN corrective action predominates (Fig5.C and 5.D).Afterwards, this corrective action is gradually decreased while the corrective action provided by MF→ DCN and PC→ DCN connections is gradually increased. The transition between these two control actions is regulated by the PC activity which in turn, is working in a constant range of frequencies thanks to MF→DCN and PC→DCN connections. We obtain a system able to self-adapt by means of a distributed learning where all the learning sites are complementary working together.

MF→DCN/PC→DCN/IO→DCN connections

Figure 5. Synaptic weight evolution during the learning process, at IO→ DCN, MF→ DCN and PC→ DCN connections when using a 10kg payload and initial parameters for a 0.5 kg payload setting. (A) Synaptic weight at MF→ DCN. (B) Synaptic weight at PC→DCN. (C) Normalized synaptic weight at IO→DCN. (D) Synaptic weight at IO→DCN.

( B )

0 0.5 1-0.1

-0.05

0

0.05

0.1

0.15

0.2

0.25

0.3

JO

INT

PO

SIT

ION

S(r

ad)

JOINT POSITIONS

-0.10

0.1 0

0.5

10.538

0.54

0.542

0.544

0.546

Y(m)

CARTESIAN POSITIONS

Z(m

)

q1

q2

q3

Benchmark Trajectory to be accomplished