Title: Transgenic CETP Dahl Salt-sensitive (Tg53) Rat Model
1Transgenic CETP Dahl Salt-sensitive (Tg53) Rat
Model
2- Victoria L. M. Herrera, M.D.
- Associate Professor of Medicine
- Section of Molecular Genetics
- Whitaker Cardiovascular Institute
- Boston University School of Medicine
- 700 Albany Street W609, Boston MA 02118
- vherrera_at_bu.edu
3Tg53 rat model is it promising enough?
- Question analyzed
- a provocative but necessary question posed by
Symposium organizers - modeling the vulnerable plaque has been an
underestimated challenge - a review of multi-species animal models of
atherosclerosis from the 1960s underscores this
challenge
4Modeling vulnerable plaque an underestimated
challenge
Analysis of coronary artery disease at end-stage plq hge plq erosn plq fissure plq thombosis occlusn
Pigeon Carneau, Show Racer aortic root nr nr nr
Monkey a. Cynomolgus b. African green c. Rhesus nr nr nr nr nr nr nr nr nr nr
Pig a. thiouracil xradn b. FHC hyperLDL-emia nr nr nr some some
Rabbit WatanabeHHL coronary ostia nr nr nr nr
Mouse ApoE/LDLr knockout nr nr nr nr
Rat Tg53 rat model
nr, not reported , present
5Elements of a promising model
- Simulation of coronary artery disease
- plaque site
- disease course
- plaque progression
- Model advantages as experimental system
- reproducibility
- duration to valid endpoints
- defined genetic background
- accessible phenotype manipulation
- Model value and potential
- as investigative instrument
- as pre-clinical platform
6Elements of a promising model
7Elements of a promising model
- Tg53 rat model simulates human coronary heart
disease (CHD) - disease course
- risk factors consistent with human CHD
- hypertension exacerbates phenotype
- atherogenic lipid profile increased total
cholesterol and triglyceride levels, low HDL,
increased VLDLc and VLDLtg, increased small LDLc - hyperlipidemia increases with age
8Elements of a promising model
- Tg53 rat model simulates human coronary heart
disease (CHD) - disease course
- decreased survival compared with non-transgenic
non-hyperlipidemic, hypertensive, Dahl S rat
controls on regular rat chow Nat Med 5 383,
1999 Mol Med 7831, 2001. - end-stage simulates cardiac endpoints of CHD
- () cardio-respiratory distress
- () signs of heart failure
9Elements of a promising model
10Elements of a promising model
11Elements of a promising model
12Elements of a promising model
13Elements of a promising model
- Tg53 rat model advantages as experimental system
- reproducibility and robustness of phenotype
- lipid profile increased total cholesterol and
triglycerides predominantly in VLDL, low HDL - culprit plaque phenotype in proximal right
coronary artery - stable occlusive plaque in smaller coronary
arteries - reasonable duration to valid endpoints
- 6-9 month range of proximal coronary plaque
development on regular rat chow eccentric
macrophage-foam cell rich plaque which progresses
to culprit plaque at endstage
14Elements of a promising model
- Tg53 rat model advantages as experimental system
- defined genetic background eliminates
differential genetic susceptibility as confounder - inbred Dahl salt-sensitive hypertensive rat
strain - accessible phenotype manipulation onset and
course of hyperlipidemia and coronary artery
disease can be experimentally manipulated - Western Type Diet (0.15 cholesterol) accelerates
onset and levels of hyperlipidemia - low salt diet (0.0038 NaCl), which reduces level
of hypertension, attenuates coronary artery
disease hence increasing survival
15Elements of a promising model
- Tg53 rat model value and potential
- identical genetic background and ability to
regulate environmental factors allows well-
controlled in vivo studies for cross-talk
pathogenesis - investigation of mechanisms of coronary plaque
development not possible in humans - methodical in vivo investigation of novel
intervention targets - maximization of genomic-based technologies aimed
at the investigation of mechanisms and targets
16Elements of a promising model
- Tg53 rat model value and potential
- coronary-specific experimental design for
coronary artery-disease studies with cumulative
evidence of vessel-specific genetic factors, the
Tg53 coronary-specific phenotype is key - combinatorial modeling well characterized inbred
rat strains allow cross-breeding for interaction
studies relevant to human disease - hypertension
- diabetes
- obesity
17Elements of a promising model
- Tg53 rat model value and potential
- as investigative tool invaluable new insight
distinct from that observed in current other
models as a beginning, - 1. prelude to culprit plaque the eccentric
macrophage foam-cell rich lesion becomes the
culprit plaque, thus experimentally capturing
the beginning of the vulnerable plaque - 2. differential pathway hypothesis proximal
vulnerable-culprit coronary lesions develop
distinct from more distal stable coronary plaques - 3. lesion heterogeneity paradigm given identical
genetic background and environmental factors,
lesion heterogeneity at end-stage reflect
stochastic endpoints of a common pathogenic
framework
18Elements of a promising model
- Tg53 rat model value and potential
- as pre-clinical platform
- identical genetic background
- regulated environmental factors
- robust coronary phenotype
- instrumentation accessibility
- rat physiological and pharmacological information
database - allow continuity of comparative analysis for
successful new intervention and prevention
strategies
19Tg53 rat model is it promising enough?
- ... cant promise the world but along with
other animal models, can together make a better
promise, - but then again, which model can be promising
enough since even humans although they are the
ultimate benchmarks make terrible models, if
not the worst, for human coronary artery disease
... - ?
20Acknowledgment
- This work is supported by grants from the
National Institutes of Health and American Heart
Association.