- Methodology article
- Open Access
Method for non-invasively recording electrocardiograms in conscious mice
© Chu et al; licensee BioMed Central Ltd. 2001
- Received: 8 May 2001
- Accepted: 25 June 2001
- Published: 25 June 2001
The rapid increase in the development of mouse models is resulting in a growing demand for non-invasive physiological monitoring of large quantities of mice. Accordingly, we developed a new system for recording electrocardiograms (ECGs) in conscious mice without anesthesia or implants, and created Internet-accessible software for analyzing murine ECG signals. The system includes paw-sized conductive electrodes embedded in a platform configured to record ECGs when 3 single electrodes contact 3 paws.
With this technique we demonstrated significantly reduced heart rate variability in neonates compared to adult mice. We also demonstrated that female mice exhibit significant ECG differences in comparison to age-matched males, both at baseline and in response to β-adrenergic stimulation.
The technology we developed enables non-invasive screening of large numbers of mice for ECG changes resulting from genetic, pharmacological, or pathophysiological alterations. Data we obtained non-invasively are not only consistent with what have been reported using invasive and expensive methods, but also demonstrate new findings regarding gender-dependent and age-dependent variations in ECGs in mice.
- Heart Rate Variability
- Reduce Heart Rate
- Fast Heart Rate
- Conscious Mouse
Although electrocardiograms (ECGs) have been obtained in conscious mice, currently reported techniques require restraint  or anesthesia and surgical implantation of telemetry devices [2,3,4]. Anesthesia, however, may depress cardiovascular function, and adequate recovery after transmitter implantation in mice is nearly 3 weeks [3,5]. Accordingly, we developed a non-invasive technique for obtaining ECGs in conscious mice by placing the animal on a platform embedded with paw-sized ECG electrodes connected to an amplifier. This method is much less traumatic, requires no anesthesia or surgery, and promotes rapid screening of large quantities of mice. ECG data we obtained non-invasively in conscious mice are comparable to those recently published using surgically implanted telemetry devices [2,4]. To test the efficacy of our system, we evaluated ECGs in mice of either sex, of several strains, and of different ages. Moreover, we tested whether our system could detect ECG alterations in response to pharmacological challenge by isoproterenol. The baseline heart rate data and responses to the β-adrenergic agonist isoproterenol we recorded non-invasively in mice are comparable to data published using invasive methods. We developed an ECG signal processing, analyzing, and database Web portal, which we named e-MOUSE™, accessible to the biotechnology community. The advantages of the ECG recording and analyses paradigm we developed are clear, given the high cost of breeding, housing, and transporting mice, and the call for comprehensive yet widely available phenotyping tests .
Electrocardiographic parameters in male and female 129/Sv, C57BL/6, and FVB conscious mice.
(n = 10)
(n = 10)
(n = 10)
(n = 10)
(n = 10)
(n = 10)
Heart Rate (bpm)
571 ± 13
689 ± 12 *
692 ± 5
741 ± 2 *
736 ± 5
706 ± 7 *
HR var (bpm)
15 ± 4
20 ± 4
12 ± 3
15 ± 3
33 ± 2
16 ± 2 *
31.9 ± 1.3
28.3 ± 0.6*
26.0 ± 0.8
24.4 ± 0.7
25.4 ± 0.6
27.7 ± 0.6 *
9.6 ± 0.3
8.5 ± 0.1*
8.1 ± 0.2
7.5 ± 0.2*
7.4 ± 0.1
7.7 ± 0.1
70.2 ± 1.8
54.7 ± 2.0*
55.4 ± 0.8
53.8 ± 0.6
53.9 ± 1.2
55.7 ± 1.4
66.7 ± 1.9
58.4 ± 1.6*
59.0 ± 0.8
58.7 ± 0.3
59.3 ± 1.2
59.9 ± 1.6
This report describes the development of a system for non-invasively recording ECGs in conscious mice; neither attachment of wires, nor anesthesia, nor surgical implantation of devices is required. Our heart rate data in conscious mice are comparable to those obtained using sutured steel wire  and chronic indwelling catheters . Our ECG measurements are comparable to those obtained using implantable telemetry devices [2,4]. This non-invasive method, standardized protocol, and Internet-accessible mouse ECG analyses software (e-MOUSE™) may reduce the heterogeneity in data collected from different laboratories .
Strain & Gender Differences in ECGs in Adult Mice
To our knowledge, this is the first study to describe gender differences in heart rate in genetically homogenous strains of conscious mice. Studies in humans [9,10] and in rats [11,12] have shown females to have faster heart rates than males, differences that disappear with age [10,13]. In C57BL/6 mice and in 129/Sv mice, we found that conscious females exhibited significantly faster heart rates than male mice. In FVB/N mice, however, we noted faster heart rates and briefer ECG time intervals in male compared to female mice. Mitchell et al., using implanted transmitters, reported slightly but insignificantly faster heart rates in male compared to female FVB mice . Gender and strain differences in heart rate may reflect differences in hormone activity, which are known to affect cardiovascular autonomic regulation differentially in males and females  and vary among mouse strains . Our strain-dependent observations agree with results of invasive studies [8,6] and support the importance of genetic factors in influencing heart rate.
Developmental Changes in ECGs in Conscious Neonatal Mice
We found that the gender differences apparent in C57BL/6 adults were absent in nursling mice. Reduced activity in newborns could contribute to reduced heart rate and heart rate variability. However, observations in quietly resting adult mice (n = 3), monitored 30 min after placement on the recording platform, of reduced heart rate (471 ± 20 bpm) and increased heart rate variability (53 ± 6 bpm) suggest that the results in neonates may be attributable to reduced sympathetic and parasympathetic signaling . The time-domain heart rate variability data we obtained non-invasively are comparable to those obtained using implanted telemetry devices [2,16]. The developmental changes in heart rate we measured in mice parallel those in human neonates [13,17], lambs , and newborn rats . Moreover, our observations in neonatal mice are in agreement with Wang et al. who reported progressive and significant shortening of R-R intervals during neonatal development . Accordingly, our approach, adaptable to the study of small mice that might otherwise die from anesthesia or surgery, might be valuable in examining developmental changes and abnormalities [13,17].
Effects of Sympathetic Stimulation in Conscious Mice
The blunted heart rate increase in response to β-adrenergic stimulation in conscious C57BL/6 female mice is consistent with gender related differences in baroreflex control of heart rate in healthy humans . Estrogen has been shown to enhance baroreflex sensitivity  and attenuate the response of heart rate to administration of isoproterenol in rats . After repeated injections of isoproterenol, heart rate decreased and the QRS duration increased significantly in male mice, but did not change in female mice. Yet, both males and females demonstrated increased sensitivity to acute isoproterenol injection after repeated administration that resulted in significant cardiac hypertrophy [23,24]. We observed a 16% increase in heart mass in both sexes after 3-days of isoproterenol treatment compared to mice treated with equivolume of saline. Although β-adrenoceptor desensitization  or reduced ATPase activity  may account for the decrease in basal heart rate in the hypertrophied male hearts, the increased sensitivity to isoproterenol may support the hypotheses of ischemia-induced activation of β-adrenoceptor kinase  or modulation of G-protein signaling to preserve adenylate cyclase activity . To our knowledge, this is the first report that describes electrocardiographic evidence of myocardial ischemia in conscious mice, although ST segment changes have characterized isoproterenol-induced ischemia in rat  and man . Why males consistently developed ST segment depression following isoproterenol administration and females did not remains unanswered. However, significant gender-related differences in the expression of glutathione S-transferases (GST) have been observed in mice, with female mice expressing significantly more of this antioxidant than male mice . In mice, isoproterenol-induced oxidative stress may be attenuated in females due to higher levels of GST .
Mice are sensitive to even modest handling [3,8] and transport [3,32]. The ECG indices we measured may reflect physiologic responses to the experimental environment relative to its home cage. We encourage a 10 min acclimation period prior to recording data to attenuate effects consequent to handling and transport. Usually mice establish contact between 3 electrodes and 3 limbs within 5 minutes after acclimation to record a continuous ECG for approximately 2 seconds. The duration of the ECG recording should be considered in the interpretation of heart rate variability . The age, gender and strain variations in heart rate may reflect age, gender and strain variations in physiologic responses to transport , handling , and adaptation to repeated measurements . Yet, the inter-strain differences in heart rate we non-invasively obtained after ECG recordings of short duration are in agreement with invasive experimental techniques intended to monitor heart rate in mice as caged [6,8]. Our measurements were made in daytime hours, disrupting the less active phases of the mouse circadian cycle. Future innovation might incorporate an array of conductive electrodes into the animals' cages to eliminate the effects of handling and transport, and perhaps enable timed recordings.
Young adult mice (9 ± 1 weeks old; 21 ± 1 g) from 3 commonly used inbred strains, C57BL/6, 129/Sv, and FVB/N (The Jackson Laboratory, Bar Harbor, ME), were housed in standard conditions within the Animal Resource Facility at the Beth Israel Deaconess Medical Center, Boston MA. Nursling C57BL/6 mice of either sex were examined at post-natal day 6 and 12 and returned to their mothers. The same mice, weaned, were examined at 3 weeks of age.
Mice were gently removed from their cages and positioned on the ECG recording platform. An array of gel-coated ECG electrodes (Red Dot; 3 M, St. Paul, MN) were embedded in the floor of the platform and spaced to provide contact between the electrodes and animals' paws. For adults, the spacing between electrodes was 3 cm, and for nurslings, the spacing was reduced to 2.5 cm. Filter paper, with openings for the electrodes, prevented mouse urine from short-circuiting the signals. The electrodes were connected to an amplifier (HP78901A, Hewlett-Packard, Andover, MA) by a shielded 3-electrode lead set (M1605A Snap, Hewlett-Packard, Andover, MA). Since even modest handling of mice may induce alterations in heart rate , each mouse was permitted to acclimatize for 10 min prior to collection of baseline data. The signals were digitized with 16-bit precision (DI-220, DATAQ Instruments, Inc., Akron, OH) at a sampling rate of 2500 samples/second. When mice were sitting or otherwise positioned such that the paws were not in contact with three electrodes, the output from the amplifier was discarded. Only data from continuous recordings of 20-30 ECG signals were used in the analyses. Data were transmitted to the mousespecifics.com Internet site (Mouse Specifics, Inc., Boston, MA) using standard file-transfer protocols for ECG signal analyses by e-MOUSE™.
Each signal was analyzed using e-MOUSE™, an Internet-based physiologic waveform analysis portal. e-MOUSE™ incorporates Fourier analyses and linear time-invariant digital filtering of frequencies below 2 Hz and above 100 Hz to minimize environmental signal disturbances. The software uses a peak detection algorithm to find the peak of the R-waves and to calculate heart rate. Heart rate variability was calculated as the mean of the differences between sequential heart rates for the complete set of ECG signals. Subsequently, determination of 1st and 2nd derivatives and algebraic "if-thens" search the ECG signals for probable P-wave peaks and onset and termination of QRS complexes. Since the T-wave is not separate from the QRS in rodent ECGs [28, 34], there have been discrepancies in the definition of the QT interval and reported values . In accord with Mitchell et al. , we routinely included the inverted and/or biphasic portions of the T-wave in our calculations of the QT interval. We defined the end of the T-wave of each signal as the point where the signal returned to the isoelectric line [1,35] [the mean voltage between the preceding P-wave and QRS interval]. The QT intervals were rate corrected (QTc) by application of the equation recommended by Mitchell et al.  for use in mice. The software plots its interpretation of P,Q,R,S, and T for each beat so that spurious data resulting from unfiltered noise or motion artifacts may be rejected. e-MOUSE™ then calculates the mean of the ECG time intervals for each set of waveforms.
To test the sensitivity of our system for describing ECG alterations in response to a drug, C57BL/6 mice were given either an intraperitoneal injection of 2.5 μg/g (-)-isoproterenol (Sigma, St. Louis, MO) (5 males, 5 females) dissolved in 0.1 ml saline or an equal volume of saline (5 males, 5 females), twice daily for 3-days. ECGs were recorded within 5 min prior to each injection and between 1 and 2 min after each injection to capture the peak of the response to the drug . After the last measurement, mice were euthanized by intraperitoneal administration of pentobarbital (150 mg/Kg), consistent with the American Veterinary Medical Association Panel on Euthanasia guidelines. Excised hearts, excluding atria and blotted dry, were then weighed.
Data are presented as the means ± SE. Comparisons between genders among strains were performed using Student's t-test for unpaired observations. Effects of isoproterenol or saline injections within groups were performed using Student's t-test for paired observations, and between group comparisons using Student's t-test for unpaired observations. Differences were considered significant with P < 0.05.
We developed a non-invasive technique for obtaining ECGs in conscious mice. We developed an Internet-accessible portal for analyses of mouse electrocardiograms. Using this system, we demonstrated significant strain, gender and age-dependent differences in electrocardiograms in mice. Moreover, we demonstrated significant gender-dependent differences in the cardiovascular response to β-adrenoceptor stimulation. Our results may suggest that the stimulatory effects of genes and drugs on cardiac function may be more profound in male or masked in female mice. This non-invasive and rapid ECG phenotyping technique may improve the quality and increase the quantity of data collected from mouse models.
Mr. Diego Yepes is gratefully acknowledged for his innovative design approaches to the ECG acquisition system. Ms. Jeanne Smith provided excellent administrative support for this project and manuscript submission. I. Amende received generous support from Förderkreis zur Verbesserung des Gesundheitswesen e.V.
- Wang L, Swirp S, Duff H: Age-dependent response of the electrocardiogram to K+ channel blockers in mice. Am J Physiol Cell Physiol. 2000, 278: C73-C80.PubMedGoogle Scholar
- Gehrmann J, Hammer PE, Maguire CT, Wakimoto H, Triedman JK, Berul CI: Phenotypic screening for heart rate variability in the mouse. Am J Physiol Heart Circ Physiol. 2000, 279: H733-H740.PubMedGoogle Scholar
- Kramer K, van Acker SABE, Voss H-P, Grimbergen JA, van der Vijgh WJF, Bast A: Use of telemetry to record electrocardiogram and heart rate in freely moving mice. J Pharmacol Toxicol Methods. 1993, 30: 209-215. 10.1016/1056-8719(93)90019-B.View ArticlePubMedGoogle Scholar
- Mitchell GF, Jeron A, Gideon K: Measurement of heart rate and Q-T interval in the conscious mouse. Am J Physiol Heart Circ Physiol. 1998, 274: H747-H751.Google Scholar
- Stiedl O, Spiess J: Effect of tone-dependent fear conditioning on heart rate and behavior of C57BL/6N mice. Behav Neurosci. 1999, 111: 703-711.View ArticleGoogle Scholar
- Desai KH, Sato R, Schauble E, Barsh GS, Kobilka BK, Bernstein D: Cardiovascular indexes in the mouse at rest and with exercise: new tools to study models of cardiac disease. Am J Physiol Heart Circ Physiol. 1997, 272: H1053-H1061.Google Scholar
- Abbott A: Database to standardize mouse phenotyping. Nature. 1999, 401: 833-10.1038/44644.View ArticlePubMedGoogle Scholar
- Blizard DA, Welty R: Cardiac activity in the mouse: strain differences. J Compar Physiol Psych. 1971, 77: 337-344.View ArticleGoogle Scholar
- Huikuri VH, Pikkujämsä SM, Airaksinen KEH, Ikäheimo MJ, Rantala AO, Kauma H, Lilja M, Kesäniemi A: Sex-related differences in autonomic modulation of heart rate in middle-ages subjects. Circulation. 1996, 94: 122-125.View ArticlePubMedGoogle Scholar
- Umetani K, Singer DH, McCraty R, Atkinson M: Twenty-four hour time domain heart rate variability and heart rate: relations to age and gender over nine decades. J Am Coll Cardiol. 1998, 31: 593-601. 10.1016/S0735-1097(97)00554-8.View ArticlePubMedGoogle Scholar
- Chandler MP, DiCarlo SE: Acute exercise and gender alter cardiac autonomic tonus differently in hypertensive and normotensive rats. Am J Physiol Reg Integ Comp Physiol. 1998, 43: R510-R516.Google Scholar
- El-Mas MM, Abdel-Rahman AA: Estrogen enhances baroreflex control of heart rate in conscious ovariectomized rats. Can J Physiol Pharmacol. 1997, 76: 381-386. 10.1139/cjpp-76-4-38110.1139/cjpp-76-4-381.View ArticleGoogle Scholar
- Harper RM, Leake B, Hodgman JE, Hoppenbrouwers T: Developmental patterns of heart rate and heart rate variability during sleep and waking in normal infants and infants at risk for the sudden infant death syndrome. Sleep. 1982, 5: 28-38.PubMedGoogle Scholar
- Piccini N, Knopf JL, Gross KW: A DNA polymorphism, consistent with gene duplication, correlates with high renin levels in the mouse submaxillary gland. Cell. 1982, 30: 205-213.View ArticlePubMedGoogle Scholar
- Sugihara G, Allan W, Sobel D, Allan KD: Nonlinear control of heart rate variability in human infants. Proc Natl Acad Sci. 1996, 93: 2608-2613. 10.1073/pnas.93.6.2608.PubMed CentralView ArticlePubMedGoogle Scholar
- Jumrussirikul P, Dinerman J, Dawson TM, Dawson VL, Ekelund U, Georgakopoulos D, Schramm LP, Calkins H, Snyder SH, Hare JM, Berger RD: Interaction between neuronal nitric oxide synthase and inhibitory G protein activity in heart rate regulation in conscious mice. J Clin Inv. 1998, 102: 1279-1285.View ArticleGoogle Scholar
- Schechtman VL, Harper RM, Kluge KA, Wilson AJ, Hoffman HJ, Southall DP: Cardiac and respiratory patterns in normal infants and victims of the sudden infant death syndrome. Sleep. 1988, 11: 413-426.PubMedGoogle Scholar
- Siimes AS, Välimäki IAT, Sarajas HSS, Sakoné K, Oja RT: Heart rate variation in relation to age and sleep state in neonatal lamb. Acta Physiol Scand. 1984, 537: 7-15.Google Scholar
- Hofer MA, Reiser MF: The development of cardiac rate regulation in preweanling rats. Psychosom Med. 1969, 31: 372-388.View ArticlePubMedGoogle Scholar
- Abdel-Rahman ARA, Merrill RH, Wooles WR: Gender-related differences in the baroreceptor reflex control of heart rate in normotensive humans. J Appl Physiol. 1994, 77: 606-613.PubMedGoogle Scholar
- Mohamed MK, El-Mas MM, Abdel-Rahman AA: Estrogen enhancement of baroreflex sensitivity is centrally mediated. Am J Physiol Reg Integ Comp Physiol. 1999, 276: R1030-R1037.Google Scholar
- Fregly MJ, Thrasher TN: Response of heart rate to acute administration of isoproterenol in rats treated chronically with norethynodrel, ethinyl estradiol, and both combined. Endocrinology. 1977, 100: 148-154.View ArticlePubMedGoogle Scholar
- Kudej RK, Iwase M, Uechi M, Vatner DE, Oka N, Ishikawa Y, Shannon RP, Bishop SP, Vatner SE: Effects of chronic β-adrenergic receptor stimulation in mice. J Mol Cell Cardiol. 1997, 29: 2735-2746. 10.1006/jmcc.1997.0508.View ArticlePubMedGoogle Scholar
- Slawson SE, Roman BB, Williams DS, Koretsky AP: Cardiac MRI of the normal and hypertrophied mouse heart. Magn Reson Med. 1998, 39: 980-987.View ArticlePubMedGoogle Scholar
- Gordon AL, Inchiosa MA, Lehr D: Isoproterenol-induced cardiomegaly: assessment of myocardial protein content, actomyosin ATPase and heart rate. J Mol Cell Cardiol. 1972, 4: 543-557.View ArticlePubMedGoogle Scholar
- Ungerer M, Kessebohm K, Kronsbein K, Lohse MJ, Richardt G: Activation of β-Adrenergic receptor kinase during myocardial ischemia. Circ Res. 1996, 79: 455-460.View ArticlePubMedGoogle Scholar
- Hammond HK, Roth DA, McKirnan MD, Ping P: Regional myocardial downregulation of the inhibitory guanosine triphosphate-binding protein (Giα2) and β-adrenergic receptors in a porcine model of chronic episodic myocardial ischemia. J Clin Invest. 1993, 92: 2644-2652.PubMed CentralView ArticlePubMedGoogle Scholar
- Bestetti RB, Oliveira JSM: The surface electrocardiogram: a simple and reliable method for detecting overt and latent heart disease in rats. Braz J Med Biol Res. 1990, 23: 1213-1222.PubMedGoogle Scholar
- Winsor T, Mills B, Winbury MM, Howe BB, Berger H: Intramyocardial diversion of coronary blood flow: effects of isoproterenol-induced subendocardial ischemia. Microvasc Res. 1975, 9: 261-278.View ArticlePubMedGoogle Scholar
- Mitchell AE, Morin D, Lakritz J, Jones DA: Quantitative profiling of tissue- and gender-related expression of glutathione S-transferase isoenzymes in the mouse. Biochem J. 1997, 325: 207-216.PubMed CentralView ArticlePubMedGoogle Scholar
- Rathore N, John S, Kale M, Bhatnagar D: Lipid peroxidation and antioxidant enzymes in isoproterenol induced oxidative stress in rat tissues. Pharmacol Res. 1998, 39: 297-303. 10.1006/phrs.1998.0365.View ArticleGoogle Scholar
- Tuli JS, Smith A, Morton DB: Stress measurements in mice after transportation. Laboratory Animals. 1995, 29: 132-138.View ArticlePubMedGoogle Scholar
- Tsuji H, Venditti FJ, Manders ES, Evans JC, Larson MG, Feldman CL, Levy D: Determinants of heart rate variability. J Am Coll Cardiol. 1996, 28: 1539-46. 10.1016/S0735-1097(96)00342-7.View ArticlePubMedGoogle Scholar
- Richards AG, Simonson E, Visscher MB: Electrocardiogram and phonogram of adults and newborn mice in normal conditions and under the effects of cooling, hypoxia, and potassium. Am J Physiol. 1953, 174: 293-298.PubMedGoogle Scholar
- Kirchhoff S, Nelles E, Hagendorff A, Krüger O, Traub O, Willecke K: Reduced cardiac conduction velocity and predisposition to arrhythmias in connexin40-deficient mice. Curr Biol. 1998, 8: 299-302.View ArticlePubMedGoogle Scholar
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