scholarly journals Effects of Perches on Behavior, Heart Rate, Body Temperature and Locomotor Activity of Caged Hens

2004 ◽  
Vol 41 (2) ◽  
pp. 120-130 ◽  
Author(s):  
Kanji Matsui ◽  
Ashraf M. Khalil ◽  
Ken-ichi Takeda
2010 ◽  
Vol 1 (1) ◽  
pp. 75-85 ◽  
Author(s):  
Claudio Signer ◽  
Thomas Ruf ◽  
Franz Schober ◽  
Gerhard Fluch ◽  
Thomas Paumann ◽  
...  

2001 ◽  
Vol 50 (5) ◽  
pp. 409-415 ◽  
Author(s):  
Megumi AKITA ◽  
Keiji ISHII ◽  
Masayoshi KUWAHARA ◽  
Hirokazu TSUBONE

2002 ◽  
Vol 51 (1) ◽  
pp. 49-56 ◽  
Author(s):  
Masashi FURUZAWA ◽  
Masayoshi KUWAHARA ◽  
Keiji ISHII ◽  
Yoichiro IWAKURA ◽  
Hirokazu TSUBONE

2011 ◽  
Vol 300 (3) ◽  
pp. R519-R530 ◽  
Author(s):  
Jens Hannibal ◽  
Hansen M. Hsiung ◽  
Jan Fahrenkrug

Neurons of the brain's biological clock located in the hypothalamic suprachiasmatic nucleus (SCN) generate circadian rhythms of physiology (core body temperature, hormone secretion, locomotor activity, sleep/wake, and heart rate) with distinct temporal phasing when entrained by the light/dark (LD) cycle. The neuropeptide vasoactive intestinal polypetide (VIP) and its receptor (VPAC2) are highly expressed in the SCN. Recent studies indicate that VIPergic signaling plays an essential role in the maintenance of ongoing circadian rhythmicity by synchronizing SCN cells and by maintaining rhythmicity within individual neurons. To further increase the understanding of the role of VPAC2 signaling in circadian regulation, we implanted telemetric devices and simultaneously measured core body temperature, spontaneous activity, and heart rate in a strain of VPAC2-deficient mice and compared these observations with observations made from mice examined by wheel-running activity. The study demonstrates that VPAC2 signaling is necessary for a functional circadian clock driving locomotor activity, core body temperature, and heart rate rhythmicity, since VPAC2-deficient mice lose the rhythms in all three parameters when placed under constant conditions (of either light or darkness). Furthermore, although 24-h rhythms for three parameters are retained in VPAC2-deficient mice during the LD cycle, the temperature rhythm displays markedly altered time course and profile, rising earlier and peaking ∼4–6 h prior to that of wild-type mice. The use of telemetric devices to measure circadian locomotor activity, temperature, and heart rate, together with the classical determination of circadian rhythms of wheel-running activity, raises questions about how representative wheel-running activity may be of other behavioral parameters, especially when animals have altered circadian phenotype.


1982 ◽  
Vol 16 (4) ◽  
pp. 319-326 ◽  
Author(s):  
D. Büttner ◽  
Franziska Wollnik

Heart rate (HR), body temperature (BT) and locomotor activity (LA) were measured continuously over 5 days in freely moving rats. In addition to the well-known circadian rhythms, all variables exhibited considerable fluctuations in amplitude mainly during the dark, but also in the light periods. The values of HR varied from 286 ± 12 to 470 ± 26 b.p.m. and BT from 36·15 ± 0·15°C to 38·45 ± 0·25°C. The large variability of HR, BT and LA within a single day was due more to large short-term fluctuations within periods of about 3-5 hours duration, than to differences between the light and the dark period. Good consistency of daily patterns and similarity of the 3 variables was found within the animals. Usually there were 3 or 4 regular peaks during the dark and often another peak 3-4 hours after the onset of light. Correlation coefficients, calculated on the basis of 5-min mean values, were highly significant ( P<0·001) for LA vs HR (0·61-0·73), LA vs BT (0·40-0·53), and HR vs BT (0·61-0·68). Between-hour correlations were higher than these common correlations of 5-min values. HR vs BT (0·76-0·83) and LA vs BT (0·63-0·79) correlated as well as LA vs HR (0·72-0·83). The short-term fluctuations (within-hours) gave lower correlation coefficients for LA vs BT (0·23-0·32) and HR vs BT (0·29-0·41) than LA vs HR (0·40-0·70). This seems to result from a physiological delay of BT relative to HR and LA.


Endocrinology ◽  
2016 ◽  
Vol 157 (12) ◽  
pp. 4654-4668 ◽  
Author(s):  
Natalia Mendez ◽  
Diego Halabi ◽  
Carlos Spichiger ◽  
Esteban R. Salazar ◽  
Karina Vergara ◽  
...  

Chronic exposure to light at night, as in shift work, alters biological clocks (chronodisruption), negatively impacting pregnancy outcome in humans. Actually the interaction of maternal and fetal circadian systems could be a key factor determining a fitting health in adults. We propose that chronic photoperiod shift (CPS) during pregnancy alter maternal circadian rhythms and impair circadian physiology in the adult offspring, increasing health risks. Pregnant rats were exposed to normal photoperiod (12 h light, 12 h dark) or to CPS until 85% of gestation. The effects of gestational CPS were evaluated on the mother and adult offspring. In the mother we measured rhythms of heart rate, body temperature, and activity through gestation and daily rhythms of plasma variables (melatonin, corticosterone, aldosterone, and markers of renal function) at 18 days of gestation. In adult offspring, we measured rhythms of the clock gene expression in the suprachiasmatic nucleus (SCN), locomotor activity, body temperature, heart rate, blood pressure, plasma variables, glucose tolerance, and corticosterone response to ACTH. CPS altered all maternal circadian rhythms, lengthened gestation, and increased newborn weight. The adult CPS offspring presented normal rhythms of clock gene expression in the SCN, locomotor activity, and body temperature. However, the daily rhythm of plasma melatonin was absent, and corticosterone, aldosterone, renal markers, blood pressure, and heart rate rhythms were altered. Moreover, CPS offspring presented decreased glucose tolerance and an abnormal corticosterone response to ACTH. Altogether these data show that gestational CPS induced long-term effects on the offspring circadian system, wherein a normal SCN coexists with altered endocrine, cardiovascular, and metabolic function.


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