A hVIPR transgene as a novel tool for the analysis of circadian function in the mouse suprachiasmatic nucleus.

A mouse bearing a novel transgene encoding the human VPAC2 receptor (hVIPR; Shen et al. (2000) PNAS, 97, 11575-11580) was used to investigate circadian function in the hypothalamic suprachiasmatic nuclei (SCN). Neurons expressing hVPAC2R, detected by a beta-galactosidase (beta-GAL) tag, have a distinct distribution within the SCN, closely matching that of neurophysin (NP) neurons and extending into the region of peptide histidine isoleucine (PHI) cells. In common with NP and PHI cells, neurons expressing hVPAC2R are circadian in nature, as revealed by synchronous rhythmic expression of mPERIOD (mPER) proteins. A population of SCN cells not expressing PHI, NP or hVPAC2R exhibited circadian PER expression antiphasic with the rest of the SCN. Nocturnal light exposure induced mPER1 in the ventral SCN and mPER2 widely across the nucleus. Induction of nuclear mPER2 in hVPAC2R cells confirmed their photic responsiveness. Having established their circadian properties, we tested the utility of SCN neurons expressing the hVIPR transgene as functionally and anatomically explicit markers for SCN tissue grafts. Prenatal SCN tissue from hVIPR transgenic pups survived transplantation into adult CD1 mice, and expressed beta-GAL, PER and PHI. Over a series of studies, hVIPR transgenic SCN grafts restored circadian activity rhythms to 17 of 72 arrhythmic SCN lesioned recipients (23.6%). By using heterozygous hVIPR transgenic grafts on a heterozygous Clock mutant background we confirmed that restored activity rhythms were conferred by the donor tissue. We conclude that the hVIPR transgene is a powerful and flexible tool for examination of circadian function in the mouse SCN.

A hVIPR transgene as a novel tool for the analysis of circadian function in the mouse suprachiasmatic nucleus.

A mouse bearing a novel transgene encoding the human VPAC2 receptor (hVIPR; Shen et al. (2000) PNAS, 97, 11575-11580) was used to investigate circadian function in the hypothalamic suprachiasmatic nuclei (SCN). Neurons expressing hVPAC2R, detected by a beta-galactosidase (beta-GAL) tag, have a distinct distribution within the SCN, closely matching that of neurophysin (NP) neurons and extending into the region of peptide histidine isoleucine (PHI) cells. In common with NP and PHI cells, neurons expressing hVPAC2R are circadian in nature, as revealed by synchronous rhythmic expression of mPERIOD (mPER) proteins. A population of SCN cells not expressing PHI, NP or hVPAC2R exhibited circadian PER expression antiphasic with the rest of the SCN. Nocturnal light exposure induced mPER1 in the ventral SCN and mPER2 widely across the nucleus. Induction of nuclear mPER2 in hVPAC2R cells confirmed their photic responsiveness. Having established their circadian properties, we tested the utility of SCN neurons expressing the hVIPR transgene as functionally and anatomically explicit markers for SCN tissue grafts. Prenatal SCN tissue from hVIPR transgenic pups survived transplantation into adult CD1 mice, and expressed beta-GAL, PER and PHI. Over a series of studies, hVIPR transgenic SCN grafts restored circadian activity rhythms to 17 of 72 arrhythmic SCN lesioned recipients (23.6%). By using heterozygous hVIPR transgenic grafts on a heterozygous Clock mutant background we confirmed that restored activity rhythms were conferred by the donor tissue. We conclude that the hVIPR transgene is a powerful and flexible tool for examination of circadian function in the mouse SCN.

Expression of clock gene products in the suprachiasmatic nucleus in relation to circadian behaviour.

Circadian timing within the suprachiasmatic nucleus (SCN) is modelled around cell-autonomous, autoregulatory transcriptional/post-translational feedback loops, in which protein products of canonical clock genes Period and Cryptochrome periodically oppose transcription driven by CLOCK:BMAL complexes. Consistent with this model, mCLOCK is a nuclear antigen constitutively expressed in mouse SCN, whereas nuclear mPER and mCRY are expressed rhythmically. Peaking in late subjective day, mPER and mCRY form heteromeric complexes with mCLOCK, completing the negative feedback loop as levels of mPer and mCry mRNA decline. Circadian resetting by light or non-photic resetting (mediated by neuropeptide Y) involves acute up- and down-regulation of mPer mRNA, respectively. Expression of Per mRNA also peaks in subjective day in the SCN of the ground squirrel, indicating common clock and entrainment mechanisms for nocturnal and diurnal species. Oscillation within the SCN is dependent on intercellular signals, in so far as genetic ablation of the VPAC2 receptor for vasoactive intestinal polypeptide (VIP) suspends SCN circadian gene expression. The pervasive effect of the SCN on peripheral physiology is underscored by cDNA microarray analysis of the circadian gene expression in liver, which involves ca. 10% of the genome and almost all aspects of cell function. Moreover, the same molecular regulatory mechanisms driving the SCN appear also to underpin peripheral cycles.

Photoperiodic control of seasonality in birds.

This review examines how birds use the annual cycle in photoperiod to ensure that seasonal events--breeding, molt, and song production--happen at the appropriate time of year. Differences in breeding strategies between birds and mammals reflect basic differences in biology. Avian breeding seasons tend to be of shorter duration and more asymmetric with respect to changes in photoperiod. Breeding seasons can occur at the same time each year (predictable) or at different times (opportunistic), depending on the food resource. In all cases, there is evidence for involvement of photoperiodic control, nonphotoperiodic control, and endogenous circannual rhythmicity. In predictable breeders (most nontropical species), photoperiod is the predominant proximate factor. Increasing photoperiods of spring stimulate secretion of gonadotropin-releasing hormone (GnRH) and consequent gonadal maturation. However, breeding ends before the return of short photoperiods. This is the consequence of a second effect of long photoperiods--the induction of photorefractoriness. This dual role of long photoperiods is required to impart the asymmetry in breeding seasons. Typically, gonadal regression through photorefractoriness is associated with a massive decrease in hypothalamic GnRH, essentially a reversal to a pre-pubertal condition. Although breeding seasons are primarily determined by photoperiodic control of GnRH neurons, prolactin may be important in determining the exact timing of gonadal regression. In tropical and opportunistic breeders, endogenous circannual rhythmicity may be more important. In such species, the reproductive system remains in a state of "readiness to breed" for a large part of the year, with nonphotic cues acting as proximate cues to time breeding. Circannual rhythmicity may result from a temporal sequence of different physiological states rather than a molecular or cellular mechanism as in circadian rhythmicity. Avian homologues of mammalian clock genes Per2, Per3, Clock, bmal1, and MOP4 have been cloned. At the molecular level, avian circadian clocks appear to function in a similar manner to those of mammals. Photoperiodic time measurement involves interaction between a circadian rhythm of photoinducibility and, unlike mammals, deep brain photoreceptors. The exact location of these remains unclear. Although the eyes and pineal generate a daily cycle in melatonin, this photoperiodic signal is not used to time seasonal breeding. Instead, photoperiodic responses appear to involve direct interaction between photoreceptors and GnRH neurons. Thyroid hormones are required in some way for this system to function. In addition to gonadal function, song production is also affected by photoperiod. Several of the nuclei involved in the song system show seasonal changes in volume, greater in spring than in the fall. The increase in volume is, in part, due to an increase in cell number as a result of neurogenesis. There is no seasonal change in the birth of neurons but rather in their survival. Testosterone and melatonin appear to work antagonistically in regulating volume.

Somatotopical organization of fos-like immunoreactivity in rat cervical spinal cord following noxious stimulation of the forelimb.

In the present study c-fos expression has been used as a marker of neuronal activation following noxious stimuli applied to one of three different sites on the forelimb in rats. In three treatment groups (n=4 animals in each group) rats were anaesthetized with barbiturate and a mechanical pinch was applied to either (i) the most medial digit, (ii) the most lateral digit, or (iii) the shoulder area of one forelimb. An additional control group (n=4) received no pinch. The presence of Fos-like immunoreactivity was used to chart the distribution of cervical spinal cord neurons activated by the stimulus. No significant difference was found in the number of labelled cells between the contralateral side of each treatment group and either side of the control group. By contrast, there was a significant increase in labelled cells between the ipsilateral and contralateral sides within each treatment group. Labelled cells were present mainly in the dorsal horn of the ipsilateral cervical spinal cord where they were clustered in laminae I and II. Clear topographical differences were also evident between treatment groups in the distribution of labelled cells. The most medial digit was represented rostromedially compared to the most lateral digit (cell peak at segmental levels C5/C6 and C7, respectively), while the shoulder stimulus produced a more widespread distribution of labelled cells which was centred rostrolaterally (peak at segmental levels C4/C5).Overall, the findings suggest that forelimb inputs to the cervical cord are organized somatotopically in a similar fashion to hindlimb inputs to the lumbar cord, although the representation of individual forelimb digits may be more extensive in the rostrocaudal axis. This difference could reflect the use of the rats' forepaws in more complex sensorimotor tasks such as grasping and exploring objects.

Numerical aspects of pontine, lateral reticular, and inferior olivary projections to two paravermal cortical zones of the cat cerebellum.

Two different olivo-cortico-nuclear zones in the cat cerebellum have been compared quantitatively as regards the numbers of cells projecting to them from within several sources of mossy fibres (MFs), namely the basal pontine nuclei (BPN), nucleus reticularis tegmenti pontis (NRTP), and the ipsilateral lateral reticular nucleus (LRN). The zones chosen were the C3 zone in lobule V of the anterior lobe and the C1 zone in pars copularis of the paramedian lobule (PMLpc), localised by recording climbing fibre-mediated potentials evoked on their surface as a result of volleys set up in their spino-olivocerebellar paths. The zones were injected with fluorescent-labelled latex microspheres and cell bodies, retrogradely labelled in the MF source nuclei and in the contralateral inferior olive, were counted and mapped. Evidence was obtained that tracer efficiency was very high in both the MF projections and the olivo-cerebellar projection and that each olivocerebellar axon may provide only one climbing fibre to the upper part of a lobule V folium but an average of nearly two to the same part of a PML folium. When the numbers of labelled cells in each MF source nucleus were expressed as a percentage of the total number of labelled pontine cells, the biggest source for lobule V was the contralateral BPN, followed by LRN, contralateral NRTP, ipsilateral BPN, and ipsilateral NRTP. For PMLpc, the order was similar except that ipsilateral BPNs exceeded contralateral NRTPs, but the dominance of contralateral BPN as a source was much greater. Cell totals were converted into projection densities (i.e., numbers of cells labelled per square millimetre of cortical sheet involved in the injection site); densities for PMLpc were found to be almost three times greater than those for lobule V for contralateral BPN but the two densities were not significantly different for ipsilateral BPN. The three other MF sources projected at higher densities to lobule V than to PML. These findings indicate that two cortical zones, both of which receive climbing fibres from the rostral part of the dorsal accessory olive and project to nucleus interpositus anterior, nevertheless differ markedly in regard to both the relative and the absolute sizes of the projections they receive from several of their most important sources of MFs.

A direct comparison of photoperiodic time measurement and the circadian system in European starlings and Japanese quail.

The extent to which circadian rhythms are involved in photoperiodic time measurement in quail is enigmatic, and earlier investigations have produced results consistent with an hourglass clock or one involving damped circadian oscillators. To address the problem further, the present authors carried out a direct comparison between the clocks in quail and those in starlings. Starlings possess strongly self-sustaining circadian oscillators. In Experiment 1, comparisons of testicular growth were made between the two species when birds were exposed to light:dark (LD) 6:30, LD 6:18, and LD 18:6. Starlings grew their testes rapidly under both LD 6:30 and LD 18:6, and they became photorefractory (under LD 6:18, the testes remained undeveloped). Quail grew their testes rapidly under LD 18:6 but did not do so under LD 6:30 or LD 6:18. In Experiment 2, entrainment of the activity rhythm under cycles of LD 6:30 was investigated by measuring the phase of the rhythm after release into constant darkness (DD). Birds were exposed to either 10 cycles or 11 cycles of LD 6:30 prior to DD. Starlings maintained their 24-h rhythmicity under LD 6:30 and always free ran from the phase of the subjective day. By contrast, quail showed circadian activity approximately 24 h after every light pulse and free ran from the phase of the last light pulse received. In Experiment 3, phase response curves (PRCs) were generated to 6-h light pulses. The species were strikingly different; starlings produced a Type 1 PRC, whereas quail produced a Type 0 PRC. More important, in quail the 6-h light pulse had the same effect regardless of circadian time and in almost every case activity free ran from the position of the 6-h light pulse. The results in quail are consistent with the photoperiodic time measurement system being based on a weakly self-sustaining (rapidly damping) circadian system that is invariably reset by 6 h of light, whereas in starlings the pacemakers are strongly self-sustaining. The results support the notion that hourglass pacemakers can be highly damped circadian pacemakers.

Utilization of nursing diagnosis in three Australian hospitals.

PURPOSE: To document nursing diagnoses on nursing care plans in an Australian context where NANDA nursing diagnoses were utilized. METHODS: An audit of 198 nursing care plans at three selected hospitals by three university lecturers involved in teaching nursing diagnosis. FINDINGS: Pain was the nursing diagnosis most often documented; the majority of other diagnoses pertained to physical problems experienced by patients. CONCLUSIONS: The results of this research add to the knowledge of nursing diagnosis utilization and have implications for the provision of nursing care and its teaching and research.

Copulation activates Fos-like immunoreactivity in the male quail forebrain.

It has been demonstrated using Fos immunocytochemistry that copulation activates specific cell populations in the mammalian brain. Prior to this study, no similar work has been carried out in birds. In mammals, Fos has identified brain circuits activated by genital (penile)/somatosensory and by olfactory/vomeronasal stimuli. Such inputs, of course, should play little or no role in birds (no penis, little or no role for olfaction) and a differential responsiveness could therefore be expected. Male Japanese quail (Coturnix japonica) were allowed to interact freely with adult females and the presence of active sexual behavior, including cloacal contact movements, was confirmed in each case. Control subjects were exposed to a domestic chick (same size as an adult quail) and no sexual behavior was observed. Copulation induced the appearance of Fos-like immunoreactive (FLI) cells in the preoptic area, the hyperstriatum ventrale, parts of the archistriatum, and the nucleus intercollicularis. Induction of FLI cells was observed throughout the rostral to caudal extent of the preoptic region of males from the level of the tractus septomesencephalicus to the level of the anterior commissure, and in the rostral part of the hypothalamus to the level of the supraoptic decussation. The FLI cells did not lie directly adjacent to the third ventricle, but were located 500-1000 microns from the ventricle wall at the level of the lateral edge of the medial preoptic nucleus or, in more caudal sections, in a position ventrolateral to the bed nucleus striae terminalis. It is unlikely that the Fos induction in males resulted from copulation-induced endocrine changes because copulation did not affect plasma levels of luteinizing hormone or testosterone. It is concluded that the responses were due to copulation-associated somatosensory inputs and/or to stimuli originating from the female.

c-fos expression in the putative avian suprachiasmatic nucleus.

c-fos induction was investigated as a potential component in the avian photic entrainment pathway and as a possible means of locating the central pacemaker in birds. In both quail (Coturnix coturnix japonica) and starlings (Sturnus vulgaris) exposure to 1 h of light induced Fos-lir in the visual suprachiasmatic nucleus but not in the medial suprachiasmatic nucleus. However, the degree of c-fos induction in the visual suprachiasmatic nucleus was similar at different circadian times despite the fact that the light pulses caused differential phase shifts in the locomotor rhythm. For golden hamsters the same experiment resulted in significantly different levels of Fos-lir in the suprachiasmatic nucleus, as well as different phase shifts. Starlings and hamsters were also entrained to T-cycles that caused a large daily phase shift (T = 21.5 h in starlings, T = 22.67 hours in hamsters), or no daily phase shift (T = free running period). No difference in the induced levels of Fos-lir in the visual suprachiasmatic nucleus region was observed between the two groups of starlings, but in hamsters there were significantly different levels of Fos-lir in the suprachiasmatic nucleus between the two groups.

An impedimetric method for rapid screening of cosmetic preservatives.

An efficient impedance method was developed for rapid evaluation of cosmetic preservatives. The method used decimal reduction time or D-value to assess preservative efficacies. The D-value, which was calculated from the plot of Log CFU ml-1 versus time by linear regression analysis, could be obtained within 48 h. Thus, the time required for the challenge test was reduced from 4-8 weeks with the standard procedures (eg US Pharmacopeia), to 2 days with the current method. A calibration curve (r = -0.95) was established by plotting the Log CFU ml-1 versus capacitance detection time (DT) of 108 samples. With the calibration, CFU can be estimated directly from the impedance test without plating. Two commercial biocides and several other chemicals were evaluated in a shampoo by the impedance procedure against Pseudomonas aeruginosa. The D-values obtained from the impedance test were not significantly different from those produced by the conventional plate count method. The technique was found to be particularly useful when screening a large number of compounds to find novel preservatives and synergistic preservative combinations.

Does unusual entrainment of the circadian system under T36h photocycles reduce the critical daylength for photoperiodic induction in Japanese quail?

In photoperiodic species, short daylength resonance cycles of modulo t + 1/2 (t = 24 h) behave like long days because they entrain the circadian system so that alternate light pulses coincide with the photoinducible phase (Oi) in castrated quail. However, while a long-day response after exposure to a single long daylength is readily detected by a rise in plasma LH (photoinduction), long-term exposure to LD 6:30 is ineffective in this respect. To discover whether this occurs because of unusual entrainment, circadian rhythms in quail and starlings were investigated. Whereas starlings entrained in the expected way with alternate pulses falling at different circadian phases, activity bouts in quail appeared to follow 24 h after successive light pulses. Because of this, activity was examined in free-running conditions to confirm that the pacemaker in quail was indeed being reset to a constant phase (reset to circadian time [CT] 0) by successive pulses. Examination of the circadian rhythms of plasma melatonin secretion under LD 6:30 also showed a resetting to CT 0. The positioning of all light pulses at the same circadian phase in the early subjective day explains the lack of photoinduction in quail since Oi in the early subjective night phase remains unilluminated. A second feature in quail is that when the length of the photophase is gradually increased within T36h cycles, there is a progressive increase in the degree of photoinduction although the photophase length remains well below the critical daylength for induction in normal T24h cycles. We therefore tested whether Oi is reset to a constant phase by successive pulses in LD 6:30, and that this phase is also advanced relative to light onset so that photophases shorter than the critical daylength can interact with Oi to cause induction. Such a reduction in critical daylength relative to successive LD 6:30 pulses was confirmed by transferring quail to various types of long day and measuring the change in LH secretion. When the long-day test was replaced with continuous light, stimulation of LH secretion occurred 5-7 h earlier in quail pretreated with LD 6:30 and LD 6:54 compared to quail pretreated with LD 6:18 or LD 6:42, implying that Oi had been markedly phase advanced under resonance cycle.

Melatonin and photoperiodic time measurement in Japanese quail (Coturnix coturnix japonica).

Artificial extension of the duration of nocturnally secreted circulating melatonin with exogenous injections produces a short day effect in the reproductive status of mammals, and this paradigm has been applied to Japanese quail to test the hypothesis that birds are similar to mammals in this respect. Male quail reared on non-stimulatory short days (8L:16D) were switched to mildly stimulatory 12L:12D and given daily melatonin injections at dusk (10 micrograms 2 h before dusk and 10 micrograms at dusk) or at dawn (10 micrograms 2 h before dawn and 10 micrograms at dawn) for about 3 weeks. Although assay of circulating melatonin suggested that injections had extended the melatonin signal, there was no short day effect, i.e. reproductive stimulation was not prevented. This reinforces the view that, unlike mammals, birds do not read the duration of the melatonin signal to measure scotoperiod. Paradoxically, however, the injections resulted in a small but significant stimulation. The results are discussed in view of the postulated role for melatonin as an internal Zeitgeber, which is coupled to the external photic Zeitgeber, to regulate the circadian system.

Ophthalmic implications of seasonal affective disorder.

A review of seasonal affective disorder (SAD) is presented with a discussion of its standard treatment of phototherapy. A number of ophthalmic implications related to SAD are proposed. These implications relate to both the condition and the phototherapy used in its treatment, especially the use of "full spectrum" light which contains ultraviolet and near ultraviolet radiation.

The 1979 revision of Z80.1--the American National Standard recommendations for prescription ophthalmic lenses--the AOA position.

Since April, 1972, the American National Standard Requirements for First-Quality Prescription Ophthalmic Lenses, Z80.1-1972, has been in the process of revision. The American National Standards Institute procedures are explained as well as details of the new revised standard. In addition, an explanation of the AOA position on the revision is given. Finally, what this standard means to the practicing optometrists is discussed.

Tolerance to tolerances: some thoughts on the 1979 American National Standard recommendations for prescription ophthalmic lenses.

The 1979 revision of the ANSI Z80.1 Ophthalmic Lens Standards resulted in rather significant changes affecting three areas of ophthalmic lens requirements: 1) central refractive characteristics, 2) prismatic characterstics, and 3) factors relating to the magnification properties of lenses. Based primarily on what an optical laboratory could consistently produce, the ANSI Ophthalmic Lens Sub-committee decided to widen some of the tolerances over those expressed in previous revisions. This paper attempts to show how these new tolerances relate to certain aspects of patient sensitivity to errors induced by ophthalmic lenses conforming with the new revision.

Effects of mydriatics and a miotic on ocular discomfort and pupil responses.

Mydriatics produced two different effects on the discomfort threshold following administration of the drugs depending upon whether the mydriasis was produced by paralysis of the sphincter muscle or by activation of the dilator. When the sphincter was paralyzed by tropicamide, the discomfort threshold was elevated during the period of time that the pupillary light reflex was significantly reduced to the flashing stimulus. Initially, phenylephrine-induced mydriasis had no effect on the discomfort threshold, but as the pupil responses returned to normal the threshold rapidly increased and then gradually returned to a pre-drug level. The return of the threshold back to normal seemed to parallel the decline of action of phenylphrine on the dilator muscle. Significant impairment of the light reflex by pilocarpine-produced miosis was also related to an increase of the discomfort threshold.