Rat (Rattus norvegicus) and spiny mouse (Acomys cahirinus) are closely related murinoid species that mainly differ in the developmental timing of birth. A comparison between the developmental profiles of some characteristic enzymes of the liver of both species was carried out to elucidate the question to what extent are these enzymic profiles and hence the maturation of the liver related to the timing of birth? It was found that these organotypic enzymes first become detectable at the same developmental stage in both species. Likewise, the weaning phase of the enzymic profiles occurs at the same developmental time point in both species. It is argued that both the first appearance and the weaning increase in enzyme activity levels occur at endogenously programmed timepoints with only superimposed effects of hormones. In contrast, the perinatal phase of the enzymic profile is completely dependent on the developmental timing of birth and therefore appears not to be anchored to a particular developmental timepoint, but rather to be dependent on birth-associated (hormonal) adaptation. In accordance with this hypothesis it was found that the morphological development of the liver proceeded independent of the timing of birth. Furthermore, the hormonal regulation of the investigated enzymes was found to be the same in both species. Despite the more advanced state of morphological development of the liver in the spiny mouse at birth, it was found that the inducibility of organotypic gene expression by hormones in spiny mouse fetuses was as limited as in rat fetuses. This observation therefore suggests that the intra-uterine environment is responsible for the limited inducibility of enzymes before birth.

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Rat (Rattus norvegicus) and spiny mouse (Acomys cahirinus) are closely related murine species that, due to their altricial (rat) and precocial (spiny mouse) modes of development, differ in the developmental timing of birth. A comparison between the developmental profiles of plasma glucagon, insulin, thyroxine, triiodothyronine, and glucocorticosteroid hormone was carried out to elucidate the question to what extent these hormonal profiles were related to the timing of birth. Although corticosterone is the major circulating glucocorticosteroid in rat, only cortisol was found in the spiny mouse. The onset of increases in glucocorticosteroid and thyroid hormone levels occurred at the same developmental time points in both species. A neonatal increase in triiodothyronine levels was observed in the spiny mouse only. In both species the immediate perinatal period was characterized by decreases in the ratio of insulin and glucagon levels and the level of glucocorticosteroids. The observed developmental patterns of hormonal levels were found to be consistent with the observed developmental pattern of enzymic maturation in the respiratory and gastrointestinal tract, which play a critical role in the adaptation to the extrauterine environment.

Rat and spiny mouse (Acomys cahirinus) are closely related murinoid species that represent altricial (rat) and precocial (spiny mouse) modes of development. The late intrauterine developmental stages of the spiny mouse therefore seem comparable to the early extra-uterine developmental stages of the rat. To elucidate the question to what extent the development of the lung is related to the developmental timing of birth, we have studied some enzymes involved in the de novo synthesis of phosphatidylcholine. Of the enzymes studied, cholinephosphate cytidylyltransferase shows peaks in activity in the perinatal period (rat and spiny mouse) and at the beginning of the 3rd postnatal week (rat only). This enzyme fulfils the requirements for a developmental parameter best as changes in activity of this enzyme can be correlated with phases of cell proliferation and surface expansion in the lung of the rat. The single peak of cholinephosphate cytidylyltransferase activity in the spiny mouse as well as microscopical examination of the lung support the hypothesis that the processes of proliferation and surface expansion, which occur consecutively in the rat, develop concurrently in the spiny mouse.

In rats, hepatic carbamoylphosphate synthase (ammonia) and arginase activities are closely related during development. Activities increase sharply during the last 4 prenatal and first 4 postnatal days and during the 3rd postnatal week. Decreases are observed between 4 and 9 days after birth, and after weaning, during adolescence. During senescence activities increase again. Before birth, treatment with prednisolone is far less effective in increasing enzyme activities than during the first 2 postnatal weeks, when it seems to precipitate normal development of the 3rd postnatal week. In the 4th postnatal week the sensitivity to prednisolone treatment increases approximately 25-fold. During the 2nd postnatal week, dexamethasone proves to be more potent, on a molar base, than triamcinolone which is more potent than prednisolone and hydrocortisone. Increases in enzyme activities which are associated with increases in blood levels of glucocorticosteroids are also associated with 2- to 3-fold decreases in DNA content, i.e. with decreases in hepatocyte multiplication rate and increases in hepatocyte cell size. These phenomena may be sequelae of quantal cell cycles leading to changes in hormone response capacity or hormone response sensitivity.