Comparative and evolutionary dimensions of the energetics of human pregnancy and lactation.

The purpose of this article is to compare the energetics of reproduction for human and other primates in order to evaluate the extent to which human reproductive energetics are distinct from other primates and other large-bodied placental mammals. The article also evaluates the energetics of human and primate gestation and lactation using data from a variety of different populations living under different environmental circumstances. Energetics refers to energy intake and expenditure, and changes in body fat stores. Human and nonhuman primates have longer periods of gestation and lactation and slower prenatal and postnatal growth than other mammals of similar size. This reduces daily maternal energy costs. The development of sizable fat stores is not unique to humans, but fat stores are typically greater in human females and may play a greater role in reproduction. The strategies used to meet the energy costs of pregnancy vary among populations of humans and nonhuman primates and among humans interindividual variability is high. In pregnancy, some increase energy intake but others apparently do not. Increases in metabolic efficiency are evident in some human populations, whereas decreases in physical activity occur, but are not seen in all human or primate populations. Lactation is more energetically costly on a daily basis among humans and nonhuman primates, but has not been as well studied. It appears that both nonhuman and human primates tend to increase energy intake to meet in part the cost of lactation. They also use other strategies such as relying on body tissue stores, reductions in physical activity, and/or increases in metabolic efficiency to meet the remainder of the cost. It is also clear that human females in different populations and different women in the same population use a different combination of strategies to meet the cost of lactation.

Analysis of dentition of a living wild population of ring-tailed lemurs (Lemur catta) from Beza Mahafaly, Madagascar.

Detailed descriptions of the dentition of many strepsirhine primate taxa are rare, despite their importance in understanding primate evolutionary biology. While several researchers have provided detailed morphological descriptions of ring-tailed lemur dentition (e.g., Schwartz and Tattersall [1985] Am. Mus. Nat. Hist. Anthropol. Pap. 60:1-100; Tattersall and Schwartz [1991] Am. Mus. Nat. Hist. Anthropol. Pap. 69:2-18), there are few studies (e.g., Eaglen [1986] Am. J. Phys. Anthropol. 71:185-201) that present quantitative data on the dentition of this species. Furthermore, prior analyses were based on museum specimens from various populations and locations. We present here quantitative and morphological data on the dentition of a population of wild Lemur catta from Beza Mahafaly Special Reserve, Madagascar. Measurements were made on dental casts (n = 39) taken from living members of this L. catta population. Our analysis indicates that no significant (P > 0.05) sexual dimorphism exists for the 30 dental measurements collected. These data support the generalizations (e.g., Plavcan and van Schaik [1994] Evol. Anthropol. 2:208-214; Kappeler [1996] J. Evol. Biol. 9:43-65) that little sexual dimorphism in dentition exists among Malagasy strepsirhines. In addition, the overall patterns of metric variation in this sample compare favorably with patterns seen among other primates, e.g., premolar measurements varying more than molars (e.g., Gingerich [1974] J. Paleontol. 48:895-903). However, there is a degree of intraspecific morphological variation indicated, with one of the morphological traits discussed in other studies as being species-specific for L. catta (absence of P(4) metaconids) observed to vary between specimens. Because the patterns of variation seen in this sample are from a known breeding population, the data presented here provide an important reference for interpreting and understanding the fossil record.

Regulation of endothelin-1 expression in normal and transfected endothelial cells.

Calcium phosphate precipitation and retrovirus-mediated infection methods were used to stably infect bovine pulmonary artery endothelial cells (BPAECs) with mammalian expression vectors bearing human prepro-ET-1 cDNA. The calcium phosphate precipitation method afforded a stably transfected cell line that expressed approximately four times higher ET-1 than untransfected BPAEC by radioimmunoassay and at the mRNA level. The retrovirus-mediated transfection method yielded stably infected clones that secreted eightfold to 10-fold higher ET-1 than the nontransfected BPAECs; one clone continued to produce 10-fold higher levels after continuous assay for 1 year. Both transfected and nontransfected cells showed an increase (approximately twofold) in ET-1 production in response to thrombin (10 U/ml). Downregulation of ET-1 production was exhibited by both transfected and nontransfected cells in response to nitric oxide (NO) donors: sodium nitroprusside (NOPr), S-nitroso-N-acetoxy penicillamine (SNAP), and acetoxime. The potentiation of NO by superoxide dismutase (SOD) also downregulated ET-1 production. These studies show that an exogenous gene introduced into a cell type that normally expresses that gene product can be regulated by agonists and antagonists in a manner similar to the normal gene regulatory mechanisms for that cell type. This is of potential importance in gene therapy experiments, where mechanisms for regulation of expression remain elusive.