A less stressful alternative to oral gavage for pharmacological and toxicological studies in mice.

[1]  M. Walker,et al.  Cytochrome P4501A1 is required for vascular dysfunction and hypertension induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin. , 2010, Toxicological sciences : an official journal of the Society of Toxicology.

[2]  Jian Wang,et al.  NFATc3 contributes to intermittent hypoxia-induced arterial remodeling in mice. , 2010, American journal of physiology. Heart and circulatory physiology.

[3]  Jian Wang,et al.  An activated renin-angiotensin system maintains normal blood pressure in aryl hydrocarbon receptor heterozygous mice but not in null mice. , 2010, Biochemical pharmacology.

[4]  S. Ferguson,et al.  Use of food wafers for multiple daily oral treatments in young rats. , 2009, Journal of the American Association for Laboratory Animal Science : JAALAS.

[5]  M. Walker,et al.  Hypertension, Cardiac Hypertrophy, and Impaired Vascular Relaxation Induced by 2,3,7,8-Tetrachlorodibenzo-p-Dioxin are Associated with Increased Superoxide , 2008, Cardiovascular Toxicology.

[6]  Aruni Bhatnagar,et al.  Environmental Risk Factors for Heart Disease , 2008, Reviews on environmental health.

[7]  M. Walker,et al.  In utero and lactational 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure: effects on fetal and adult cardiac gene expression and adult cardiac and renal morphology. , 2008, Toxicological sciences : an official journal of the Society of Toxicology.

[8]  Daniel W. Jones,et al.  Recommendations for blood pressure measurement in humans and experimental animals: Part 1: blood pressure measurement in humans: a statement for professionals from the Subcommittee of Professional and Public Education of the American Heart Association Council on High Blood Pressure Research. , 2005, Hypertension.

[9]  A. K. Hansen,et al.  The welfare impact of gavaging laboratory rats , 2005, Animal Welfare.

[10]  Chad B. Sandusky,et al.  Laboratory routines cause animal stress. , 2004, Contemporary topics in laboratory animal science.

[11]  S. Whitesall,et al.  Comparison of simultaneous measurement of mouse systolic arterial blood pressure by radiotelemetry and tail-cuff methods. , 2004, American journal of physiology. Heart and circulatory physiology.

[12]  R. Palme,et al.  Analyzing corticosterone metabolites in fecal samples of mice: a noninvasive technique to monitor stress hormones , 2004, Hormones and Behavior.

[13]  R. Palme,et al.  Effects of sex and time of day on metabolism and excretion of corticosterone in urine and feces of mice. , 2003, General and comparative endocrinology.

[14]  H P Voss,et al.  Telemetric monitoring of blood pressure in freely moving mice: a preliminary study , 2000, Laboratory animals.

[15]  K Kramer,et al.  A new method for measurement of blood pressure, heart rate, and activity in the mouse by radiotelemetry. , 2000, Journal of applied physiology.

[16]  B. Levine,et al.  Stress produced by gavage administration in the rat. , 2000, Contemporary topics in laboratory animal science.

[17]  J. White,et al.  The influence of restraint on blood pressure in the rat. , 1997, Journal of pharmacological and toxicological methods.

[18]  S. Schantz,et al.  Learning in monkeys exposed perinatally to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). , 1989, Neurotoxicology and teratology.