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Brazilian Journal of Medical and Biological Research

Print version ISSN 0100-879XOn-line version ISSN 1414-431X

Braz J Med Biol Res vol.36 no.2 Ribeirão Preto Feb. 2003

https://doi.org/10.1590/S0100-879X2003000200016 

Braz J Med Biol Res, February 2003, Volume 36(2) 273-278 (Short Communication)

Circadian rhythms in blood pressure in free-ranging three-toed sloths (Bradypus variegatus)

D.P.F. Duarte, V.L. Silva, A.M. Jaguaribe, D.P. Gilmore and C.P. Da Costa

Departamento de Fisiologia e Farmacologia, Universidade Federal de Pernambuco, Recife, PE, Brasil

Abstract
Text
References
Acknowledgments
Correspondence and Footnotes


Abstract

Blood pressure (BP) profiles were monitored in nine free-ranging sloths (Bradypus variegatus) by coupling one common carotid artery to a BP telemetry transmitter. Animals moved freely in an isolated and temperature-controlled room (24ºC) with 12/12-h artificial light-dark cycles and behaviors were observed during resting, eating and moving. Systolic (SBP) and diastolic (DBP) blood pressures were sampled for 1 min every 15 min for 24 h. BP rhythm over 24 h was analyzed by the cosinor method and the mesor, amplitude, acrophase and percent rhythm were calculated. A total of 764 measurements were made in the light cycle and 721 in the dark cycle. Twenty-four-hour values (mean ± SD) were obtained for SBP (121 ± 22 mmHg), DBP (86 ± 17 mmHg), mean BP (MBP, 98 ± 18 mmHg) and heart rate (73 ± 16 bpm). The SBP, DBP and MBP were significantly higher (unpaired Student t-test) during the light period (125 ± 21, 88 ± 15 and 100 ± 17 mmHg, respectively) than during the dark period (120 ± 21, 85 ± 17 and 97 ± 17 mmHg, respectively) and the acrophase occurred between 16:00 and 17:45 h. This circadian variation is similar to that observed in cats, dogs and marmosets. The BP decreased during "behavioral sleep" (MBP down from 110 ± 19 to 90 ± 19 mmHg at 21:00 to 8:00 h). Both feeding and moving induced an increase in MBP (96 ± 17 to 119 ± 17 mmHg at 17:00 h and 97 ± 19 to 105 ± 12 mmHg at 15:00 h, respectively). The results show that conscious sloths present biphasic circadian fluctuations in BP levels, which are higher during the light period and are mainly synchronized with feeding.

Key words: Sloths, Bradypus, Circadian rhythm, Blood pressure


Sloths, mammals belonging to the family Bradypodidae, inhabit the tropical forests of Central and South America. They are of particular interest to researchers because of their low pattern of motor activity as well as their extremely slow movement. The sloths' curious postural behavior can be clearly observed during most of the time when they remain suspended from the branches of trees.

Previous measurements of blood pressure (BP) in unanesthetized sloths have been carried out in laboratory situations with the animals placed in an experimental chair (1-6). In these studies, BP levels were lower than those recorded by Johansen et al. (7) in immobilized but unanesthetized sloths. The cardiovascular adjustments to tilting (1,2,5) and the BP and heart rate (HR) responses to the injections of catecholamines and autonomic drugs (4,6) were exaggerated and qualitatively different in comparison with those observed in other mammals. Increases (1) or falls (3) in BP were observed in response to the approach used by different investigators, showing the sensitivity of these species to the presence of humans.

A circadian rhythm in BP has been demonstrated in various species of mammals, including rats (8,9), rabbits (9), cats (10), dogs (11), marmosets (12) and mice (13). These studies have contributed to a better understanding of the behavior and physiology of these animals.

In the present study we used biotelemetry to examine BP changes in free-ranging sloths (Bradypus variegatus) to determine the pattern of circadian rhythms during an artificial light-dark cycle, and how the cardiovascular system of these animals is affected by changes in behavior in the absence of direct human influence. Biotelemetry is an extremely valuable research tool which can be used to study unanesthetized animals over a prolonged period of time without the interference of an investigator.

Biotelemetric measurements of BP were recorded in adult sloths (4.4 ± 0.6 kg), four males and two females, over a period of 48 h and in three males over a period of 26 h. A total of 1485 recordings were obtained, each lasting 1 min. In the latter three males, the trials were interrupted for technical reasons (clotting and loss of the BP signal).

Sloths were obtained from the wild in the vicinity of Recife, PE, Brazil, and kept in the vivarium at the university for two weeks before being used. The animals were observed and weighed daily and the different aspects of their behavioral repertoire were noted as described by Silva (14) for free-ranging sloths. This included postural habit, as well as feeding and motor activity. On the day prior to surgery the animals were shaved in the appropriate regions for placement of silver plate electrodes to record the electrocardiogram (ECG) in lead II as described by Duarte et al. (1). Records of ECG were utilized as an index of postsurgical stress.

Sloths have a rete mirabile in their limbs which prevents the use of peripheral cannulation for BP studies. Therefore, the surgical technique described by Duarte et al. (1) was utilized for cannulation of the common carotid artery. Under local anesthesia with 10 ml 2% xylocaine (Astra Química do Brasil, São Paulo, SP, Brazil), a midline incision was made in the anterior neck region and the right common carotid artery was isolated and cannulated. The catheter was filled with heparinized physiological saline (Liquemine, Produtos Roche e Químicos e Farmacêuticos, Rio de Janeiro, RJ, Brazil).

Twenty-four hours after surgery the animals were dressed in a jacket with a pocket in which the BP telemetry transmitter was placed. The transmitter, previously calibrated, was attached to an arterial catheter and the animals were able to roam freely in an experimental room with controlled 12/12-h artificial light/dark cycles (lights on at 6:00 h). The room had dimensions of 4.5 x 3.0 x 3.5 m and had a large branched tree trunk in the middle of the floor which was available for climbing and moving. Ambient temperature was maintained at 24ºC. Water and food (fresh embauba leaves) were available ad libitum. The BP signals, sampled at 200 Hz, were collected for 1 min at intervals of 15 min for a 24-h period. Animals were observed for behavioral activity (resting, eating and moving) through a unidirectional visor placed in the experimental room. Resting behavior was classified in one of two ways, as defined by Moura Filho et al. (15) from their studies on sleep-wake cycles in B. variegatus. These were a) "awake-alert" with the head raised, the eyes open and showing occasional blinks, and b) "behavioral sleep" during which the animal remained suspended, or else seated with the head raised and the eyes closed or with the head down on the chest and encircled by one or both of the forelimbs. Feeding behavior was defined as spontaneously eating fresh embauba leaves. Moving behavior was recorded when the animal was moving along the branches of the trees or dragging itself forward on the ground.

Systolic (SBP) and diastolic (DBP) blood pressures were calculated heartbeat to heartbeat using the Windaq 200 Calculate software (Dataq Instruments, Akron, OH, USA) and presented in Excel software. Mean BP (MBP) was calculated as DBP plus one third of the difference between SBP and DBP. The data are reported as means ± SD.

Statistical analysis was performed by two-way ANOVA for comparisons of the mean levels of SBP, DBP and MBP on different experimental days and of individual mean values for each animal, i.e., each animal represents one group of values. The Tukey test was used to determine significant differences between groups.

The COSANA software was used to analyze BP rhythms and a cosine curve was constructed using the cosinor method (the least square cosine fitting) as modified by Benedito-Silva (16), to show patterns of changes in BP over 24 h. The fitted period was set at 24 h, and the mesor (midline-estimating statistic of rhythm, overall 24-h mean) and amplitude (one half of the total cosine excursion) were calculated.

Statistical significance of the difference in mean HR before and after surgery and of the measurements of SBP, DBP and MBP related to the dark-light cycle was determined by the Student t-test. The level of significance was defined at P<0.05. At the conclusion of the study, the cannulae were removed and, after a period of recovery, the sloths were released back into the wild.

The animal experiments were carried out with previous approval of the Ethics Committee of Centro de Ciências Biológicas, Universidade Federal de Pernambuco and with license from Instituto Brasileiro de Meio Ambiente (IBAMA, No. 075/98-DIFAS).

Mean HR values before (70 ± 17 bpm) and after (73 ± 16 bpm) surgery were not significantly different (P>0.05, paired Student t-test), suggesting that the animals were unstressed.

Mean SBP, DBP and MBP values during the experimental period were 121 ± 22, 86 ± 17 and 98 ± 18 mmHg, respectively. These levels did not change significantly during the days of experimentation (P>0.05, F(2.1482) = 1.69). The comparative statistical analysis of individual MBP values showed that they differed from one another (F(8.1476) = 201.80, P<0.001 for SBP, F(8.1476) = 211.70, P<0.01 for DBP and F(8.1476) = 214.76, P<0.001 for MBP), although only one male exhibited high SBP (151 ± 14 mmHg), DBP (102 ± 8 mmHg) and MBP (125 ± 9 mmHg) in comparison to the other eight sloths (P<0.001, Tukey test). However, these values could not be explained by any aberrant behavior, since the behavior of this animal was similar to that observed in the others.

The present findings demonstrate that the levels of BP in free-ranging B. variegatus were similar to those obtained by Duarte et al. (1) in sloths kept in an experimental chair and to those found in other mammals including rats (8,9), cats (10) and dogs (11), but higher than measured in rabbits (9). While differences were recorded between individual sloths, the overall changes in BP levels over 24 h showed similar patterns throughout the period of monitoring.

Although various aspects of the physiology and behavior of the animal do change over time, certain patterns of rhythmicity are apparent. These are generated by the body's internal clock, which acts to ensure that the different physiological systems will always function at optimal levels. Among the various external stimuli, termed synchronizers or zeitgebers, that entrain the endogenous circadian rhythms of BP, the most important is the light-dark cycle (17).

In the present study the levels of BP recorded in sloths over a 2-day period revealed clear circadian variation (Figure 1). Spontaneous variations (increase and decrease) in BP levels occurred without any evident relationship to external stimuli. These changes showed that there was ample fluctuation in BP levels over 24 h. As can be seen in Figure 1, the standard deviation of SBP was larger than that of DBP and MBP, showing greater lability of this parameter. BP levels were significantly higher (P<0.05, unpaired Student t-test) in the light than in the dark period (SBP, 125 ± 21 vs 120 ± 21 mmHg; DBP, 88 ± 15 vs 85 ± 17 mmHg, and MBP, 100 ± 17 vs 97 ± 17 mmHg, respectively). Higher BP levels have been observed during the light period in cats (10), dogs (11), and marmosets (12), and during the dark period in rats and rabbits (9). Thus, Bradypus presents a clear circadian variation of BP similar to that recorded in the former three groups of mammals.

The cosine curve, for SBP, DBP and MBP (Figure 2) showed a mesor value (mean ± SEM) of 121 ± 0.8, 90 ± 0.6 and 104 ± 0.6 mmHg, amplitude of 14 ± 1, 11 ± 0.8 and 12 ± 0.9 mmHg, an acrophase value of 16:32 ± 0:22, 17:13 ± 0:34 and 16:54 ± 0:28 h, and a percent rhythm of 32, 36 and 34%, respectively. The mesor levels are similar to those obtained in rats, but higher than those found in rabbits (9). However, the SBP and DBP amplitudes were around four- and three-fold higher, respectively, than those observed in both of these species (SBP: 3.3 ± 0.3 mmHg for rabbits and 3.1 ± 0.3 mmHg for rats; DBP: 2.8 ± 0.2 mmHg for rabbits and 3.6 ± 0.2 mmHg for rats) showing a lability in their levels in B. variegatus.

In mammals, the diurnal and nocturnal patterns of BP result from neuroendocrine changes associated with alterations in mental and physical activity over a 24-h period. In diurnally active mammals BP is higher during the day, falling at night during sleeping (18). Observations on sloths during the present study showed that different bouts of behavior occupied their time as follows: "behavioral sleep" (67%), "awake-alert" (24%), feeding (7%), and moving (2%). "Behavioral sleep" was observed during both the light and dark periods, but predominated in the latter; "awake-alert", eating and moving were more common during the former. "Behavioral sleep" showed the highest incidence between 21:00 and 8:00 h, eating at 17:00 h, and moving at 15:00 h. "Behavioral sleep" was accompanied by a fall in BP (MBP down from 110 ± 19 to 90 ± 19 mmHg; P<0.05, unpaired Student t-test). Both feeding and moving increased BP (MBP up from 96 ± 17 to 119 ± 17 mmHg during eating, and from 97 ± 19 to 105 ± 12 mmHg during moving; P<0.001, paired Student t-test).

Among the several investigators who have studied biological and behavioral rhythms in sloths, there are divergences of opinion related to the motor activity pattern and sleep duration of these animals (14). Previous studies by Sunquist and Montgomery (19) indicated that the genus Bradypus does not have a cyclic pattern of diurnal and nocturnal activity, although a reduction in activity was observed at the end of the dark period. They suggested that this behavior resulted from a decrease in ambient temperature at that time. Studies evaluating sleep patterns in sloths through the electroencephalogram demonstrated that they sleep about 16 h per day, including the period of early morning (15). In the present study we observed that, although BP levels were highest during the light period (with the acrophase occurring between 16:00 and 17:45 h), the batiphase was also recorded during the same period (7:30 h). This suggests that these animals may be sleeping at this time, since sleep is known to be associated with a significant reduction in BP; however, room temperature remained constant at 24ºC, thus precluding any effect of changes in ambient temperature on activity.

The present experiments on free-ranging sloths (B. variegatus) demonstrate the existence of a biphasic circadian fluctuation in BP with the highest level observed during the light period. The fact that this occurred on successive days indicates that the animals were chronobiologically adjusted to the experimental conditions. The acrophase of BP, occurring during the light period between 16:00 and 17:45 h, seems to be synchronized mainly with feeding (17:00 h). Although a circadian rhythm in BP was clearly demonstrated, the existence of others not examined in the present study, such as an ultradian rhythm (probably involved in BP lability) or perhaps an infradian rhythm, cannot be ruled out.


Figure 1. Variations correlated with time of day in systolic (SBP), diastolic (DBP) and mean (MBP) blood pressure in unanesthetized sloths, Bradypus variegatus, over a period of two days.

[View larger version of this image (49 K GIF file)]


Figure 2. A cosine curve, constructed using COSANA software, illustrating the circadian rhythm in mean (MBP), diastolic (DBP) and systolic (SBP) blood pressure in one representative free-ranging sloth, Bradypus variegatus, over a period of two days. The line indicates the cosine fit and the points indicate the individual values of blood pressure.

[View larger version of this image (24 K GIF file)]


References

1. Duarte DPF, Da Costa CP & Huggins SE (1982). The effects of posture on blood pressure and heart rate in the three-toed sloth (Bradypus tridactylus). Comparative Biochemistry and Physiology, 73A: 697-702.        [ Links ]

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Acknowledgments

Special thanks are due to the students André Vieira, Ana Katarina Gomes and Dinani Matoso for technical assistance.


Correspondence and Footnotes

Address for correspondence: D.P.F. Duarte, Departamento de Fisiologia e Farmacologia, UFPE, Av. Professor Morais Rego, s/n, 50670-901 Recife, PE, Brasil. Fax: +55-81-3271-8530. E-mail: dfittipaldi@bol.com.br

Presented at the 34th International Congress of Physiological Sciences, Christchurch, New Zealand, August 2001. Research supported by the Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco (FACEPE). Received January 4, 2002. Accepted September 30, 2002.

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