Polytetrafluoroethylene toxicosis in recently hatched chickens (Gallus domesticus)

Two groups of chickens (Gallus domesticus; White Leghorn; age, 4 d and 2 wk) housed in a university research vivarium were found dead or moribund without prior signs of illness. The overall mortality rates were 92.3% (60 of 65 birds) for the 4-d-old birds and 80% (8 of 10) for the 2-wk-old birds. All chicks were housed in brooders with heat lamps in a temperature- and humidity-controlled room. Primary gross findings were mild to moderate dehydration and hepatic lipidosis. The most consistent histologic findings were pulmonary hemorrhage and edema in all 7 of the 4-d-old birds evaluated and in all 4 of the 2-wk-old birds assessed. In addition, 1 of the 4-d-old birds had multifocal centrilobular hepatic necrosis. These findings suggested an inhaled toxicant and hypoxia, respectively. Inspection of the animal room revealed that approximately 50% of the heat lamp bulbs in the brooder cage were coated with polytetrafluoroethylene (PTFE). Two published case reports detail similar experiences in birds exposed to PTFE-coated heat-lamp bulbs. Birds are highly sensitive to inhaled toxicants owing to the high efficiency of their respiratory systems, and PTFE toxicosis is known to cause pulmonary edema and hemorrhage in pet birds after exposure to overheated nonstick cookware. In the present case, the bulbs were replaced, and no similar problems subsequently have been noted. This case illustrates the sensitivity of avian species to respiratory toxicants and serves as a reminder that toxicosis can be encountered even in the controlled environment of a laboratory vivarium.     

C-3 Amido-indole cannabinoid receptor modulators

C-3 Amido-indoles were found to selectively bind to the CB2 receptor. SAR studies led to optimized compounds with excellent in vivo potency against LPS induced TNF-alpha release in murine models of cytokine production.     

SAR of psilocybin analogs: discovery of a selective 5-HT 2C agonist

An SAR study of psilocybin and psilocin derivatives reveals that 1-methylpsilocin is a selective agonist at the h5-HT(2C) receptor. The corresponding phosphate derivative, 1-methylpsilocybin, shows efficacy in an animal model for obsessive-compulsive disorder, as does 4-fluoro-N,N-dimethyltryptamine. These results suggest a new area for development of novel 5-HT(2C) agonists with applications for drug discovery.     

Estimating the strength of sexual selection from Y-chromosome and mitochondrial DNA diversity

We show that a sex difference in the opportunity for selection results in sex differences in the strength of random genetic drift and thus creates different patterns of genetic diversity for maternally and paternally inherited haploid genes. We derive the effective population size Ne for a male-limited or female-limited haploid gene in terms of I, the "opportunity for selection" or the variance in relative fitness. Because the variance in relative fitness of males can be an order of magnitude larger than that of females, the Ne is much smaller for males than it is for females. We derive both nonequilibrium and equilibrium expressions for F(ST) in terms of I and show how the portion of I owing to sexual selection, Imates, that is, the variation among males in mate numbers, is a simple function of the F's for cytoplasmic (female inherited) and Y-linked (male inherited) genes. Because multiple, transgenerational data are lacking to apply the nonequilibrium expression, we apply only the equilibrium model to published data on Y chromosome and mitochondrial sequence divergence in Homo sapiens to quantify the opportunity for sexual selection. The estimate suggests that sexual selection in humans represents a minimum of 54.8% of total selection, supporting Darwin's proposal that sexual selection has played a significant role in human evolution and the recent proposal regarding a shift from polygamy to monogamy in humans.     

Don'T throw bateman out with the bathwater!

Bateman identified two aspects of sexual selection. The first,called Bateman's principle, is that sexual selection favorsincreased promiscuity of males but not of females as a resultof differences in parental investment in gametes. The secondis that the variance in mate number of males is the fundamentalcause of a sex difference in fitness variance. We argue thatBateman's insight about the source of sexual selection is morefundamental than his speculation about patterns of parentalinvestment. We show that, when the sex ratio is 1:1, the averagefemale must be as promiscuous as the average male, because eachcopulation involves one male and one female. Because mean maleand female promiscuity are tied together in the same manneras mean male and female fitness, a sex difference in matingpropensity must be the result of either (1) a sex differencein the covariance between matings and number offspring, or (2)Fisherian run-away sexual selection, wherein female reluctanceto mate is a weak form of female choice. We show how femalepromiscuity can limit the evolution of male promiscuity, turningthe central argument of parental investment theory on its head.     

An abnormality in sebaceous function in phenylketonuria.

The sebum excretion rate has been found to be increased in female patients with phenylketonuria. This may be related to a depletion of midbrain dopamine and release of the sebotrophic hormone.     

Partial purification of a low molecular weight inhibitor of epidermal DNA synthesis

Abstract. An attempt has been made to purify factors present in aqueous extracts of pig epidermis which inhibit epidermal cell proliferation. A lipophilic factor of low molecular weight (less than 10,000), has been shown to inhibit DNA synthesis as measured by the uptake of tritiated thymidine in mouse ear epidermis. Purification by alcohol precipitation, ethyl acetate extraction and silicic acid column chromatography produced a fifteen-fold increase in the specific activity of the inhibitory action. It seems likely that aggregation or absorption of this low molecular weight factor may explain the high molecular weight of epidermal cell proliferation inhibitors previously studied, as well as the difficulty in their characterization.     

Alpha-MSH and coat color changes in the mouse

The effect of -MSH on coat color was examined in viable yellow mice (C3H/He-A*^vy). These mice normally grow a coat of darkly pigmented hair at puberty. This darkening effect was also evident in hair that grew in a region that had been plucked at 13 days of age. Administration of -MSH increased the darkness of this hair and the hair which grew naturally in an unplucked area. However, the natural coat darkening that occurred at puberty was not associated with an increase in plasma immunoreactive -MSH levels. Moreover, although bromocryptine, a dopamine agonist that inhibits -MSH release from the pituitary reduced the darkness of the coat that grew after plucking the reduction in coat darkening was unrelated to changes in plasma -MSH. Nevertheless, this effect of bromocryptine was reversed when -MSH was administered together with the drug. Apomorphine had no effect on coat darkening and produced only a slight decrease in plasma -MSH. Melatonin reduced coat darkening slightly but, like apomorphine, had little effect on plasma -MSH concentrations. Although -MSH may have a physiological role in coat darkening in the C3H/He-A*^vy mouse at puberty the response seems to be unrelated to an increase in circulating -MSH. Thus, other factors, such as changes in melanocyte sensitivity to -MSH or inhibitory mechanisms that prevent coat darkening during prepubertal and adult life may be involved in regulation of coat color in the viable yellow mouse.