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2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping Resources Basic Mouse Neurobehavioral Exam (or how to give a mouse a physical) Julie Watson MA Vet MB DACLAM • Samuel Irwin - First Phenotyping Screen – Psychopharmacologia (Berl.) 13 222-257 (1968) • Jacqueline Crawley – Crawley,J and Paylor,R. Hormones & Behavior 197-211 (1997) – “What’s Wrong with my Mouse?” Wiley-Liss 2000. • SHIRPA stage I – Mamm Genome. 1997 Oct;8(10):711Rogers DC, Fisher EM, Brown SD, Peters J, Hunter AJ, Martin JE • Websites: – Eumorphia http://www.eumorphia.org/EMPReSS/servlet/EMPReSS.Frameset – MRC Mutagenesis Program http://www.mgu.har.mrc.ac.uk/facilities/mutagenesis/mutabase/ SHIRPA Goals • SmithKline Beecham Pharmaceuticals • Harwell, MRC Mouse Genome Centre and 1. Detect abnormalities likely to affect future behavioral tests Mammalian Genetics Unit • Imperial College School of Medicine at St • Mary's Royal London Hospital, St Bartholomew's and the Royal London School of Medicine Phenotype – Blindness – Physical defects – Deafness • • Assessment Effect of Background Strain Age-related hearing loss & vestibular defects (<3m) • • • • • Many 129 strains A/J C57BR, C57L DBA I, LP, NOD, ALR, ALS • C57BL/6J @12-18m Blindness (rd1 gene) • • • • • • • • FVB C3H BUB CBA SJL SWR NON P, PL Goals (2) 2. Suggest further testing – Presence of abnormal behaviors – Absence of normal behaviors – Motor or neurological deficits 1 2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping Behavioral Phenotyping Level 1 Screen Accession #_________ Date ________Investigator ____________________Genotype ___________________________________ Pitfalls • Variations due to: – Husbandry methods (see John Crabbe, Science 1999) – Individual mouse variables Age/sex/background strain/social dominance – Environment: Noise/temperature/humidity/location etc. – Testing conditions: Location, time of day • Detect only sizeable deficits – Background strain not inbred. F1’s, N2’s – Are controls comparable ? – Insufficient numbers • Statistical analysis ? - ordinal data Background strain(s)_____________Inbred / N#___ Tg /TM KO/KI/Cond Key: 0 = zero; 1 = slow or reduced; 2 = normal; 3 = hyper Animal # WT Hemi -/Animal # WT DOB/Age Sex Sex Weight (g) Condition Score Empty Cage 2 mins: Gait abnormal Y Posture abnormal Y Freezing Y Wild running Y Stereotypies Y Escape Y Fur color N N N N N N M F DOB/Age Weight (g) Condition Score Exploring 0..1..2..3 Empty Cage 2 mins: 0= <1 side; 1 =< 1 circuit; Gait abnormal Y N 2= multiple circuits; 3= frantic Posture abnormal Y N Freezing Y N Digging 0..1..2..3 Wild running Y N Grooming 0..1..2..3 Stereotypies Y N Rearing 0..1..2..3 Escape Y N DORSAL Hemi Exploring 0..1..2..3 0= <1 side; 1 =< 1 circuit; 2= multiple circuits; 3= frantic Digging Grooming Rearing 0..1..2..3 0..1..2..3 0..1..2..3 VENTRAL DRAW Bald patches/abnormalities Bald patches? Y.. N Piloerection? Y..N DRAW Bald patches/abnormalities Bald patches? Y.. N Piloerection? Physical abnormality Y..N Y..N Physical abnormality Y..N Whisker damage -/M F Fur color DORSAL VENTRAL Y..N Whisker damage Y..N Body tone 0..1..2..3 Whisker response Body tone 0..1..2..3 Whisker response NA 0..1..2..3 NA 0..1..2..3 Petting escape 0..1..2..3 Ear twitch 0..1..2..3 Petting escape 0..1..2..3 Ear twitch 0..1..2..3 Passivity 0..1..2..3 Palpebral reflex 0..1..2..3 Trunk curl 0..1..2..3 Forelimb place Righting 0..1..2..3 Visual placing 0..1..2..3 0 ..1...2...3 RL withdraw 0..1..2..3 Biting Reach c touch 0..1..2..3 Clicker NA Grip: >60 • Genotyping reliability ? Gene Name_____________ Passivity 0..1..2..3 Palpebral reflex 0..1..2..3 Trunk curl 0..1..2..3 Forelimb place 0 ..1..2..3 Righting 0..1..2..3 RL withdraw 0..1..2..3 0..1..2..3 Visual placing 0..1..2..3 Biting 0..1..2..3 0..1..2..3 Reach c touch 0..1..2..3 Clicker 0..1..2..3 <60 time _______ Grip: >60 <60 time _______ Notes: _______________________________________________________________________________ ____________________________________________________________________________________ Biosafety Cabinet Initial Information Simple Equipment Observation in Cage – Gait, posture, general appearance – Are normal behaviors present? • Exploring, thigmotaxis, digging, grooming, rearing – Are abnormal behaviors present? • freezing, wild running, stereotypies, seizures, pruritus WEIGHT PERTINENT INFORMATION TESTER BLINDED TO GENOTYPE 2 2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping Digging Rearing/Escape Subtle Deficits Obvious Deficits Limited Rearing Abnormal Behavior Physical Exam Ulcerative Dermatitis • Pick up, record abnormal physical features – Whisker loss, bald patches • barbering, fighting, dermatitis – Unkempt haircoat, piloerection • sick mouse – Eyes, legs, tail • Genetic/congenital defects, fighting 3 2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping Normal Whiskers Barbering Ref. Kalueff et al. Behavioral Processes 2005 • Usual: barbering by socially dominant mouse – Requires cooperation • All mice in cage may barber if e.g. overcrowding stress • More social barbering = less physical aggression • Whiskers are important – Bitten off, not pulled out – Used for object & texture discrimination – Exploration, balance and orienting Tests of General Reactivity Whisker loss Four Tests • • • • Normal Response to Approach Response to approach Body tone Petting escape Passivity Normal Body Tone 4 2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping High Body Tone Petting Escape Unusual Escape Attempts Passivity Tests of Postural Reactions and Reflexes Trunk Curl • • • • Trunk curl Righting reflex Forelimb proprioceptive positioning Rearlimb withdrawal 5 2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping Righting Reflex Proprioceptive Positioning Withdrawal - Fast Withdrawal - Slow Tests of Facial Nerve: Sensory & Motor Ear Twitch • Ear twitch • Whisker response • Palpebral reflex (V, VII) 6 2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping Ear Twitch – Whole Head Response Whisker Response Palpebral Response Sight • Placing – visual II • Placing – tactile Visual Placing Tactile Placing 7 2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping Hearing Test Clicker Clicker Other Tests Test for Provoked Aggression • Provoked Aggression • Grip Strength Grip Strength Normal Grip Strength Abnormal 8 2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping Impact of Whisker Deficits, Pruritus on Behavioral Tests Impact of Blindness on Behavioral Tests • Lack of Whiskers – Anxiety tests e.g. visual cliff, elevated T maze – • Learning and memory tests • Water maze, contextual fear conditioning – – – – animal cannot learn? has limited spatial abilities? Consider alternatives 2 lever or hole-poke test in operant chamber • Skew response compared with mice with whiskers • ? Remove whiskers • Itchy skin (B6 dermatitis) – open field, aggression • hyperirritability, • increased activity • increased aggression • Anxiety tests • Visual cliff, elevated T maze, light- dark box – Low anxiety? Impact of Hearing Deficits on Behavioral Tests Examples of Further Testing • Cued fear conditioning – Measures ability to learn and remember auditory cue • Alternative: contextual fear conditioning • Ability to recognize and remember place • Prepulse inhibition – Startle reflex to loud sound inhibited by quieter sound that immediately precedes it – Measure of sensorimotor gating (filtering out irrelevant material by brain) • • • • • • Open Field Light Dark Box Elevated Plus Maze Accelerating Rotarod Cued and Contextual Fear Conditioning Morris Water Maze • Alternative: use puff of air instead of tone Open Field Light Dark Box • Test of anxiety • Conflict between exploring novelty and avoiding light open spaces •General test of motor activity •Infrared beams or video •Distance traveled •Pattern of movement •Discrete movements e.g. rearing • Strain variations • Responsive to anxiolytics 9 2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping Elevated Plus Maze •Test of anxiety: prefers dark enclosed arms •Score entries into arms over 5 min trial •Anxiolytics increase entries into open arms - widely used in drug discovery Accelerating Rotarod 1. Single trial - motor coordination and balance • 4-40 rpm over 5 mins • Latency to fall 2. Successive trials – motor learning PICTURE CREDITS: EUROPEAN MOLECULAR BIOLOGY LABORATORY Cued and Contextual Conditioning Morris Water Maze •Learning and memory test •Pair footshock with auditory cue – see freezing behavior •Day 2 return to same chamber – Freezing = memory of place - i.e. contextual fear Opaque water bath Containing hidden platform Visual cues •Move to different chamber, test freezing (control for context) •Give auditory cue in new chamber – freezing = memory of tone - cued fear Probe Trial Did they Learn? Computer Tracking via video camera •Most stressful test – do last •Pretraining – place on hidden platform •Training – 60 sec swims to find platform, then time on platform •Train until WT make criteria (e.g. <10 secs to find platform) • Probe trial Visual Cliff •Test of sight – plexiglass cover to apparent cliff •Place on border •10 trials – see which way steps off •Relies on ability to see cliff •Original research showed blind strain 50/50 •Vs. sighted strains 80% on solid side •Confounded by other senses (whiskers) 10 2006 Johns Hopkins Phenotyping Symposium Watson Clinical Phenotyping Acknowledgements • • • • • • Janice Clements Christian Newcomer Jacqueline Crawley Michela Gallagher Cory Brayton Nadine Forbes Questions? 11