ampakine compounds for the treatment of rett syndrome mark a varney chief scientific officer

15
AMPAKINE Compounds for the Treatment of Rett Syndrome Mark A Varney Chief Scientific Officer

Upload: laurel-pitts

Post on 25-Dec-2015

220 views

Category:

Documents


1 download

TRANSCRIPT

AMPAKINE Compounds for the Treatment of Rett Syndrome

Mark A VarneyChief Scientific Officer

2

Hypothesis

• Depressed Levels of BNDF Contribute to the Phenotype of Rett Syndrome – Lifespan

– Motor Activity

– Cortical Layer V Firing

– Breathing Abnormalities

• Increase Brain BDNF to Attenuate Rett Symptoms

Chang et al, 2006. Neuron 49, 341–348Wang et al, 2006. J Neurosci 26:10911–5

3

BDNF – A Major Regulator of SynapticPlasticity

• Synthesized and stored in glutamatergic neurons and is released in an activity-dependent manner

• Critical for neuronal survival and differentiation

• Plays a role in fast excitatory synaptic transmission and synaptic plasticity, including LTP and LTD

• Critical for synaptic plasticity and memory processing in the adult brain

4

Strategy

• Treat with AMPAKINE Molecules to Increase Endogenous BDNF Levels in Specific Brain Regions– AMPAKINEs are small molecules that

positively modulate the AMPA receptor

5

AMPA Receptors Play a Key Role in Glutamatergic Transmission

• Glutamate is the major excitatory neurotransmitter in the CNS

• Virtually all neurons express glutamate receptors

• Fast excitatory transmission is mediated by AMPA receptors

Swanson et al. (2005)Nat Rev Drug Dis 41: 131-144

6

AMPAKINE Molecules

• AMPA receptors deactivate and/or desensitize extremely rapidly (~2-10 ms)

• AMPAKINEs are allosteric positive modulators of the AMPA receptor

– Attenuate deactivation and/or desensitization of AMPA receptors

– Strengthen synaptic transmission and facilitate long term potentiation (LTP), widely regarded as the substrate for memory

– Stimulate BDNF production

Deactivation Desensitization1 ms Pulse 500 ms Pulse

Baseline + AMPAKINE Superimposed Baseline + AMPAKINE Superimposed

Deactivation Desensitization1 ms Pulse 500 ms Pulse

Baseline + AMPAKINE Superimposed Baseline + AMPAKINE Superimposed

7

AMPAKINE Treatment

Acute Effects

(Lasts with the t½ of the drug)

•Memory •Cognition•Psychiatric disorders

Chronic Effects

(Trophic induction lasting

≥ one day)

•Memory •Cognition•Psychiatric disorders•Degenerative diseases

AMPAKINEs Have Acute and Chronic Effects In Vivo

8

1. Brief treatment with

AMPAKINE causes long

lasting increases in BDNF

2. Use daily injections of short half-life AMPAKINEs to

chronically increase BDNF levels.

3. BDNF then promotes plasticity and neuronal viability

Chronic Effects of AMPAKINEs

9

Chronic Effects of AMPAKINEs on BDNF

Rat Cortical Cultures Cultured Hippocampal Slices In Vivo

0.00

0.05

0.10

0.15

0.20

0.25

0.30

Ctrl

10uM

CX92

9

25uM

CX92

9

50uM

CX92

9

100u

M C

X929

mRNA

3 hr AMPAKINE pulse, mRNA at 18 hrs

Protein

1 injection/day for 7 days, Hippocampus collected 24

hrs after last treatment

Protein

6 hr AMPAKINE pulse, protein at 24 hrs

10

Huntington’s Disease (HD)

• Progressive, hereditary brain disease that causes changes in movement, thinking and behavior

• Onset commonly between ages 30-50• 30,000 people in US (~1/10,000)• Caused by excessive CAG repeats in the

huntingtin gene • Disturbances in executive function are

probably earliest manifestation• Neuropathology, particularly in striatum, in

later phases• BDNF levels are reduced in HD postmortem

brain and transgenic mouse models

11

Reduced BDNF and Defective LTP in Asymptomatic HD Knock-in Mice

Lynch et al., J. Neurosci 2007

TBS: 10 bursts of 4 pulses 100 Hz; separated by 200 msec

12

AMPAKINE Treatment Paradigm

HD Knock-in Mice

Injected with Vehicle or CX929 at 5 mg/kg/day i.p. for

between 4 to 30 days

18-24 hours after the last dose, measure•Hippocampal LTP•Actin Polymerization•Locomotor Effects•BDNF Measurements•Cognition

CX929 selected because of its short t½ of 15min and robust effects on BDNF

13

CX929 Up-regulates Mature BDNF in HD Knock-in Mice and Restores LTP

Mature hippocampal BDNF and LTP assayed 18 hrs after the last of 30 daily treatments with CX929

0

20

40

60

80

100

120

140

% C

ontr

ol M

ea

n

Normal HD HD+CX929

Mature HippocampalBDNF Protein

Hippocampal LTP

•Cognitive deficits restored and motor deficits prevented by CX929

14

Current Studies

• Evaluate if AMPAKINE treatment corrects Rett phenotypes in Mecp2-/y mice– Respiration

– BDNF levels

– Other behaviors

15

Summary

• AMPAKINE molecules increase brain BDNF levels

• Transgenic HD mice have deficits in BDNF levels and deficits in hippocampal LTP– The short acting AMPAKINE, CX929 can restore

depressed BDNF levels and hippocampal LTP deficits

• Rett Mice have deficits in BDNF

• Currently testing AMPAKINEs in Rett mice to see if it restores normal phenotype