Analysis of organ physiology in transgenic mice

被引:64
作者
Rao, S
Verkman, AS
机构
[1] Univ Calif San Francisco, Inst Cardiovasc Res, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94143 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2000年 / 279卷 / 01期
关键词
rodent; surgery; anesthesia; cardiovascular; lung; kidney; brain;
D O I
10.1152/ajpcell.2000.279.1.C1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The increasing availability of transgenic mouse models of gene deletion and human disease has mandated the development of creative approaches to characterize mouse phenotype. The mouse presents unique challenges to phenotype analysis because of its small size, habits, and inability to verbalize clinical symptoms. This review describes strategies to study mouse organ physiology, focusing on the cardiovascular, pulmonary, renal, gastrointestinal, and neurobehavioral systems. General concerns about evaluating mouse phenotype studies are discussed. Monitoring and anesthesia methods are reviewed, with emphasis on the feasibility and limitations of noninvasive and invasive procedures to monitor physiological parameters, do cannulations, and perform surgical procedures. Examples of phenotype studies are cited to demonstrate the practical applications and limitations of the measurement methods. The repertoire of phenotype analysis methods reviewed here should be useful to investigators involved in or contemplating the use of mouse models.
引用
收藏
页码:C1 / C18
页数:18
相关论文
共 169 条
[101]   SCOPE AND PERSPECTIVES OF INTRAVITAL MICROSCOPY - BRIDGE OVER FROM IN-VITRO TO IN-VIVO [J].
MENGER, MD ;
LEHR, HA .
IMMUNOLOGY TODAY, 1993, 14 (11) :519-522
[102]   Chronic hypertension and altered baroreflex responses in transgenic mice containing the human renin and human angiotensinogen genes [J].
Merrill, DC ;
Thompson, MW ;
Carney, CL ;
Granwehr, BP ;
Schlager, G ;
Robillard, JE ;
Sigmund, CD .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (04) :1047-1055
[103]  
Merritt A. M., 1980, Veterinary gastroenterology, P247
[104]   ACCURATE MEASUREMENT OF INTESTINAL TRANSIT IN THE RAT [J].
MILLER, MS ;
GALLIGAN, JJ ;
BURKS, TF .
JOURNAL OF PHARMACOLOGICAL METHODS, 1981, 6 (03) :211-217
[105]   SALIVARY BETA(2)-MICROGLOBULIN IN NZB/WF1 MICE [J].
MOGI, M ;
KAGE, T ;
CHINO, T ;
HARADA, M .
ARCHIVES OF ORAL BIOLOGY, 1995, 40 (04) :361-364
[106]   Effects of short-term (2 weeks) streptozotocin-induced diabetes on acetylcholine and noradrenaline in the salivary glands and secretory responses to cholinergic and adrenergic sialogogues in mice [J].
Murai, S ;
Saito, H ;
Masuda, Y ;
Nakamura, K ;
Michijiri, S ;
Itoh, T .
ARCHIVES OF ORAL BIOLOGY, 1996, 41 (07) :673-677
[107]  
Nagler RM, 1998, HEAD NECK-J SCI SPEC, V20, P58
[108]   HEREDITARY VASOPRESSIN-RESISTANT URINARY CONCENTRATING DEFECTS IN MICE [J].
NAIK, DV ;
VALTIN, H .
AMERICAN JOURNAL OF PHYSIOLOGY, 1969, 217 (04) :1183-&
[109]   Angiotensinogen gene null-mutant mice lack homeostatic regulation of glomerular filtration and tubular reabsorption [J].
Okubo, S ;
Niimura, F ;
Matsusaka, T ;
Fogo, A ;
Hogan, BLM ;
Ichikawa, I .
KIDNEY INTERNATIONAL, 1998, 53 (03) :617-625
[110]  
OLSON ME, 1988, LAB ANIM SCI, V38, P299