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Biomedical subjects

I Zucker

Publications and source records attributed to I Zucker.

At least 127 records · Page 7Linked to original sources

Suprachiasmatic nuclei influence circannual and circadian rhythms of ground squirrels.

Golden-mantled ground squirrels, maintained under constant conditions of photoperiod and temperature sustained lesions of the suprachiasmatic nuclei (SCN) or of the medial basal hypothalamus. Destruction of the SCN eliminated or disrupted circadian activity rhythms and shortened the period of the circannual reproductive cycle. Circannual body weight cycles were eliminated or disrupted in several SCN-lesioned animals and one squirrel had a 3- to 5-mo body weight rhythm; however, most SCN-lesioned squirrels with disrupted circadian activity cycles manifested normal circannual body weight rhythms. The SCN are important for circadian organization of locomotor activity of this diurnal rodent, but the generation and expression of circannual body weight and reproductive rhythms can proceed in the absence of coherent circadian organization. The SCN are less essential for the generation and expression of circannual than of circadian cycles.

Animals↗

Photoperiodic regulation of body mass, food intake, and reproduction in meadow voles.

Adult male voles were maintained for 10 wk in long or short photoperiods (14 or 10 h of light/day). A third group of animals housed in the long photoperiod was implanted with capsules containing melatonin. Body weight and food intake were measured weekly; various tissues were weighed and analyzed at the time of autopsy. After 10 wk, voles in the short photoperiod weighed 20% less and consumed 30% less food than those housed in the long photoperiod. Total body water and lean body mass were reduced in the short-day animals, although the size of the brown adipose tissue was not affected. White adipose tissue lipoprotein lipase (LPL) activity was markedly reduced in the short-day voles who also manifested gonadal regression and suppression of spermatogenesis. Melatonin mimicked the effects of short photoperiods on LPL activity and on lean body mass; other parameters for melatonin-treated animals were intermediate between those of untreated long- and short-day voles. We hypothesize that winter weight losses experienced by meadow voles in the field are mediated by decreases in the duration of the daily photophase and that the reduction in body mass permits overwintering voles to reduce their energy requirements and the amount of time devoted to foraging. At least part of the seasonal decline in body mass appears due to a decrease in gonadal hormone secretion.

Adipose Tissue, Brown↗

Photoperiod and melatonin influence seasonal gonadal cycles in the grasshopper mouse (Onychomys leucogaster).

Development of the reproductive apparatus was delayed in grasshopper mice maintained from birth in short photoperiods (10 h light/day). The inhibitory effects of short photoperiods on sexual maturation eventually waned and mice in 10L:14D became reproductively active. Adult mice transferred from long (14 h light/day) to short photoperiods underwent testicular regression after 10 weeks and complete gonadal redevelopment after 30 weeks. A similar phenomenon was observed in adult female mice; oestrous cycles ceased within 3 weeks and resumed after 13 weeks in the short photoperiod. The regressive effects of short photoperiods on the male reproductive system were mimicked by daily injections of melatonin administered to mice housed in 14L:10D. Responsiveness of the female reproductive system to melatonin was reduced among photorefractory as compared to photosensitive mice. We suggest that the initial rate of sexual maturation and the timing of seasonal breeding in adult mice are regulated by photoperiod; effects of short daylengths on the neuroendocrine-reproductive axis appear to be mediated by the pineal gland.

Animals↗

Influence of photoperiod, nutrition and water availability on reproduction of male California voles (Microtus californicus).

Male California voles were maintained in long (14L:10D) or short photoperiods (10L:14D) for 10 weeks and fed a standard diet of rabbit chow and water ad libitum. One additional group in each photoperiod received the standard diet plus supplements of spinach 3 times weekly. A fifth group was housed in 14L:10D and fed the standard diet, but for 10 weeks water availability was restricted to several hours each morning. Testes and seminal vesicles were heaviest in long-day voles fed spinach supplements and lightest in short-day voles fed only the standard diet; the latter animals manifested reduced testicular spermatogenesis. Testicular weights were also depressed in voles with restricted access to water. It is suggested that photoperiods that simulate those of winter induce regression of the reproductive organs of male California voles but the availability of green vegetation counteracts the inhibitory effects of short daylengths.

Animals↗

Photoperiodic regulation of testis function in rats: mediation by a circadian mechanism.

Laboratory rats traditionally are classified as nonphotoperiodic because variations in daylength have little or no effect on their gonadal function. After olfactory bulbectomy, however, rats show clear evidence of photoperiodic regulation of the gonads. The present study demonstrates, by means of resonance experiments, that the testicular response to daylength in rats is mediated by a circadian photoperiodic time measurement system similar to that of photoperiodic rodents. Olfactory-bulbectomized rats were maintained in fixed photoperiods in which a 6 h light period was coupled with dark periods of 18, 30, 42, or 54 h (6L:18D, 6L:30D, etc.); a fifth group was maintained in a 45L:10D photoperiod. Rats from the 6L:30D, 6L:54D and 14L:10D photoperiods had testes and seminal vesicle weights, plasma testosterone titers and spermatogenesis indices indicative of functional reproductive status. Rats exposed to the 6L:18D and 6L:42D photoperiods had reduced testicular and seminal vesicle weights, lower testosterone levels and reduced spermatogenesis. We hypothesize that photo- and nonphotoperiodic rodent species use similar mechanisms for distinguishing long from short photoperiods, but differ in the extent to which discrimination of short daylengths is transduced into altered gonadal activity.

Animals↗

Photoperiodic inhibition of testicular development is mediated by the pineal gland in white-footed mice.

White-footed mice were maintained in short or long photoperiods from birth to 60 days of age (10 h vs. 14 h of light per day). Testes weights and spermatogenesis were substantially reduced in short daylengths. Pinealectomy at 5-7 days of age eliminated the suppressive effect of photoperiod on the reproductive system. However, testicular development was not retarded in intact males kept from 25 to 60 days of age in short daylengths. Exposure to short daylengths prior to 25 days of age contributes to photoperiodic inhibition of testicular development. Removal of the pineal gland did not consistently affect gonadal maturation in long photoperiods. The pineal gland transduces the effects of short daylengths on reproductive development. Some effects of long daylengths on the neuroendocrine axis of white-footed mice may also be mediated by the pineal gland.

Animals↗

Circannual rhythms of plasma testosterone and luteinizing hormone levels in golden-mantled ground squirrels (Spermophilus lateralis).

Male squirrels, born approximately June 1 and kept under constant conditions of photoperiod (14 h of light per day) and temperature (23 +/- 2 degrees C) from birth, manifested circannual rhythms in plasma testosterone (T) and luteinizing hormone (LH) levels. Blood samples were collected once per month for 22 months and hormone levels determined by radioimmunoassay. Testosterone levels were low or undetectable ( less than or equal to 0.05 ng/ml) between October and January of the first year, and began increasing in February and peaked during April and May (approx. 4.5 ng/ml). By August of the second year T had declined to low levels which were maintained through January (0.05 ng/ml). The cycle then repeated, with T titers elevated during April and May of the second year. LH levels were undetectable (less than or equal to ng/ml) throughout most of the first 8 months of life; LH peaks were reached by individual animals between March and July. There was a close correspondence between seasonal peaks and troughs of testosterone and those in LH. The circannual pattern of plasma T and LH also was documented for a group of field-trapped males (less than or equal to 11 months old) maintained under similar conditions and bled at monthly intervals for 14 consecutive months. Rhythms of plasma T and LH persisted with a period of 11 to 12 months under constant conditions and thus qualify as circannual cycles.

Aging↗

Circannual body weight rhythms of ground squirrels: role of gonadal hormones.

The influence of ovarian and testicular hormones on circannual body weight cycles was assessed in golden-mantled ground squirrels (Spermophilus lateralis), maintained in a LD 14:10 photoperiod at 23 degrees C. Animals were gonadectomized or sham operated at 47 days of age and implanted with empty capsules or capsules filled with estradiol benzoate (EB) or testosterone propionate (TP). Body weight, food intake, and reproductive condition were recorded at weekly intervals. Gonadectomized and intact squirrels of both sexes manifested robust circannual rhythms of body weight; cyclic secretion of gonadal hormones was not necessary for the expression of this circannual cycle. Intact and gonadectomized males weighed substantially more than their female counterparts but only during part of the annual cycle. This sex difference waxed and waned on a circannual basis in the absence of concurrent gonadal hormone secretions. EB phase-delayed attainment of peak body weights in ovariectomized squirrels but did not affect timing of trough body weights. EB increased the amount of food consumed by ovariectomized squirrels particularly during the weight gain phase. TP accelerated attainment of trough body weights in orchidectomized animals. Gonadal hormones modify the magnitude and timing of body weight peaks and troughs but are not necessary for the generation or expression of the circannual body weight cycle or for the sex difference in this cycle.

Animals↗

Hamster activity and estrous cycles: control by a single versus multiple circadian oscillator(s).

Running activity onset and estrous onset were recorded for hamsters exposed to progressively shorter daily light/dark (T) cycles. The period of the estrous cycle was a quadruple multiple of the period of the activity rhythm during entrainment to T cycles of 23.5-21.5 hr. There was no evidence of desynchronization of the activity and estrus rhythms. The very short estrous periods shown during exposure to short T cycles indicate that an intrinsic 96-hr interval for ovarian follicular maturation does not determine the period of the estrous cycle. Dissociation of estrous and running activity onsets occurred for all hamsters: estrous onset generally preceded running activity onset for T greater than or equal to 23.0 hr; for shorter T cycles, estrous onset generally lagged behind running activity onset. Wheel-running activity was intermittently split into entrained and free-running components for one female: at T = 22.0 hr, estrous onset was coupled first with one and then with the other of the split activity components. These findings suggest that two or more separate circadian oscillators may control timing of the activity and estrous rhythms.

Animals↗

Photoperiodic control of reproduction in olfactory-bulbectomized rats.

30-day-old male rats were (1) sham-operated or subjected to (2) removal of the olfactory bulbs, (3) olfactory bulbectomy and blinding (4) olfactory bulbectomy and pinealectomy or (5) olfactory bulbectomy, blinding and pinealectomy. Animals were exposed from 30 to 110 days of age to long-day (14 h of light per day) or short-day (8 h of light per day) photoperiods. The reproductive system of neurologically-intact rats was not affected by exposure to short days. Nor did bulbectomy affect the reproductive system of rats exposed to long days. However, bulbectomized, short-day rats had significantly lower body weights, reduced testicular and seminal vesicle weights and lower plasma testosterone levels than did bulbectomized, long-day rats. The effects of short-day exposure on bulbectomized rats were prevented by pinealectomy. Short-day exposure and blinding exerted similar effects in bulbectomized rats. The testes of rats from all groups contained elongated spermatids; blinding and short-day treatment had no effect on spermatogenesis. Neither mating behavior nor the number of young sired was influenced by photoperiod in bulbectomized or intact rats. Removal of the olfactory bulbs unmasks photoperiodic responsiveness in rats; the antigonadal effects of short-day exposure are mediated by the pineal gland in bulbectomized rats as in species traditionally designated photoperiodic. The mechanisms by which bulbectomy renders rats responsive to short days are considered.

Animals↗

Sex differentiation of t-e circadian system in the golden hamster.

The effect of estradiol benzoate (EB) on free-running circadian activity rhythms was studied in gonadectomized hamsters maintained in constant dim illumination. EB shortened the period (tau) of the female, but not of the male circadian activity rhythm. Responsiveness of the circadian system to EB was subject to sexual differentiation. The circadian period of wheel running by female hamsters given a single injection of testosterone propionate on the day of birth did not shorten in response to EB in adulthood. This failure to respond to EB also was observed in normal male hamsters, and was different from the response shown by normal females. Preliminary data suggest that tau of the activity rhythm of males castrated on the day of birth is shortened during EB treatment in adulthood. The differential effects of estradiol on tau are related to anatomic differences between the sexes in neural connections of the substrate for circadian rhythms.

Animals↗