Action Research: Its History and Relationship to Scientific Methodology

Scientific Methodology (SM) has long suited those who favour analytical and quantitative research in management. Thus the dilemma between the rigour and relevance of contemporary management research methods is fuelled by action researchers who keep wanting to contrast Action Research (AR) with SM. This paper presents a Western philosophical view on the development of belief systems and theory-based methods over time. It thus links the progressive and cumulative development of SM with the contemporary AR methodology. In doing this it presents a different point of view—that the traditions of SM and AR have much closer relationships than people often give them credit for.     

Endonuclease G is a novel determinant of cardiac hypertrophy and mitochondrial function

Left ventricular mass (LVM) is a highly heritable trait and an independent risk factor for all-cause mortality. So far, genome-wide association studies have not identified the genetic factors that underlie LVM variation, and the regulatory mechanisms for blood-pressure-independent cardiac hypertrophy remain poorly understood. Unbiased systems genetics approaches in the rat now provide a powerful complementary tool to genome-wide association studies, and we applied integrative genomics to dissect a highly replicated, blood-pressure-independent LVM locus on rat chromosome 3p. Here we identified endonuclease G (Endog), which previously was implicated in apoptosis but not hypertrophy, as the gene at the locus, and we found a loss-of-function mutation in Endog that is associated with increased LVM and impaired cardiac function. Inhibition of Endog in cultured cardiomyocytes resulted in an increase in cell size and hypertrophic biomarkers in the absence of pro-hypertrophic stimulation. Genome-wide network analysis unexpectedly implicated ENDOG in fundamental mitochondrial processes that are unrelated to apoptosis. We showed direct regulation of ENDOG by ERR-α and PGC1α (which are master regulators of mitochondrial and cardiac function), interaction of ENDOG with the mitochondrial genome and ENDOG-mediated regulation of mitochondrial mass. At baseline, the Endog-deleted mouse heart had depleted mitochondria, mitochondrial dysfunction and elevated levels of reactive oxygen species, which were associated with enlarged and steatotic cardiomyocytes. Our study has further established the link between mitochondrial dysfunction, reactive oxygen species and heart disease and has uncovered a role for Endog in maladaptive cardiac hypertrophy.     

Relationship between climatic conditions and the relative abundance of modern C3 and C4 plants in three regions around the North Pacific

Using −24‰ and −14‰ as the endpoints of stable carbon isotopic composition of total organic carbon (δ¹³C_TOC) of surface soil under pure C₃ and C₄ vegetation, and surface soil δ¹³C_TOC data from eastern China, Australia and the Great Plains of North Amer- ica, we estimate the relative abundance of C₃/C₄ plants (i.e., the ratio of C₃ or C₄ biomass to local primary production) in modern vegetation for each region. The relative abundance of modern C₃/C₄ vegetation from each region is compared to the corresponding climatic parameters (mean annual temperature and precipitation) to explore the relationship between relative C₄ abundance and climate. The results indicate that temperature controls the growth of C₄ plants. However, even where temperature is high enough for the growth of C₄ plants, they will only dominate the landscape when precipitation declines as temperatures increase. Our results are consistent with those of other investigations of the geographic distribution of modern C₄ plant species. Therefore, our results provide an important reference for interpretation of past C₃/C₄ relative abundance records in these three regions.     

Analysis of vasodilatation in the submaxillary gland using potentiators of acetylcholine and kinins

Zusammenfassung Nachweis, dass bei Reizung des N. chorda lingualis der Katze ein Blutdruckeffekt ausbleibt, wenn ein Bradykinin potenzierender Faktor (Präparat BPF) zuvor gegeben wurde.

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Acknowledgments. We are greatly indepted to Dr.J. Stewart of the University of Colorado and to Dr.L. Greene of Brookhaven National Laboratories, New York, for kind gifts of synthetic bradykinin potentiators.

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This work was supported by grants from the Medical Research Council of Canada and the Alberta Heart Foundation.     

How did brains evolve?

Three reports on mammalian brain evolution analyse the same comparative data on brain component volumes but come to partially conflicting conclusions. Clark et al. conclude from their analysis of volumetric brain proportions ("cerebro-types") that cerebellum size is invariant across mammalian taxonomic groups, the neocortex and cerebellum do not co-vary in size (in contradiction to ref. 1), and cerebrotype-based measures identify directional changes in brain architecture. Here I provide evidence that calls each of these conclusions into question. The failure of the cerebrotype measure to identify species differences in brain architecture that are independent of gross brain size undermines the proposal by Clark et al. that it could be useful for detecting evolutionary patterns and phylogenetic relationships.     

Role of paternal and maternal genomes in mouse development

There has been much speculation on whether mammalian eggs with two male pronuclei can develop normally. Eggs with two female pronuclei can sometimes develop as far as the 25-somite stage but with only very meagre extraembryonic tissues. We suggested that the genome undergoes specific imprinting during gametogenesis and that some paternal genes may be necessary for normal development of the extraembryonic tissues, in which only the maternal X chromosome remains active. However, the need for the maternal genome for development to term is not yet unequivocally established. The detailed study described here demonstrates that while between 40 and 50% of heterozygous reconstituted eggs with a male and a female pronucleus develop to term, none of the eggs with two male pronuclei does so. Furthermore, embryos in the latter case are very retarded, even though the trophoblast develops relatively well compared with embryos having two female pronuclei. Our combined results indicate that while the paternal genome is essential for the normal development of extraembryonic tissues, the maternal genome may be essential for some stages of embryogenesis.     

Herpesvirus latency confers symbiotic protection from bacterial infection

All humans become infected with multiple herpesviruses during childhood. After clearance of acute infection, herpesviruses enter a dormant state known as latency. Latency persists for the life of the host and is presumed to be parasitic, as it leaves the individual at risk for subsequent viral reactivation and disease. Here we show that herpesvirus latency also confers a surprising benefit to the host. Mice latently infected with either murine gammaherpesvirus 68 or murine cytomegalovirus, which are genetically highly similar to the human pathogens Epstein-Barr virus and human cytomegalovirus, respectively, are resistant to infection with the bacterial pathogens Listeria monocytogenes and Yersinia pestis. Latency-induced protection is not antigen specific but involves prolonged production of the antiviral cytokine interferon-gamma and systemic activation of macrophages. Latency thereby upregulates the basal activation state of innate immunity against subsequent infections. We speculate that herpesvirus latency may also sculpt the immune response to self and environmental antigens through establishment of a polarized cytokine environment. Thus, whereas the immune evasion capabilities and lifelong persistence of herpesviruses are commonly viewed as solely pathogenic, our data suggest that latency is a symbiotic relationship with immune benefits for the host.