Senescence is the internal physiological deterioration that accompanies advancing age. Evolutionary hypotheses predict that rates of senescence should vary directly with extrinsic mortality and inversely with fecundity. If so, naked mole-rats (Heterocephalus glaber) should live a long time (senesce slowly) because in nature they inhabit heavily protected burrows, and large, old breeding females make disproportionate reproductive contributions. In addition H. glaber has an exceptionally low metabolic rate, which may reduce oxidative stress. We have maintained naked mole-rats in captivity since 1974. Here we report that individuals can live a very long time: many are alive after more than 20 years and some are 26 years old (and counting). Although we do not yet know how long naked mole-rats can live, they already are older than the maximum longevity of all but one of 156 rodent species that have been maintained in captivity from birth to death.

Agonistic and sexual interactions as well as plasma bioactive luteinizing hormone (LH) concentrations were monitored in all the adults of two colonies of the naked mole-rat Heterocephalus glaber at three phases in the pregnancy of the breeding female. Blood samples were collected at early (days 1–15), mid (days 30–40) and late (days 55–65) phases of her pregnancy, and the circulating basal plasma LH and the response to administration of 0.1 μg gonadotrophin-releasing hormone (GnRH) were examined. In both colonies it was found that non-breeding males and females showed depressed basal LH concentrations and responses to a GnRH challenge. However, there was considerable variation between individuals, in terms of both basal plasma and post-GnRH concentrations of LH, implying that certain individuals were more suppressed than others. The responses were more pronounced in non-breeding males than in non-breeding females, and this is discussed in light of the reproductive skew occurring within colonies. Few agonistic interactions occurred between the breeding female and the majority of the colony members, and overall, there was no clear relationship between plasma LH and the amount of aggression received from the breeding female. However, in one colony there was a significant positive correlation between basal plasma LH concentrations of non-breeding females and agonistic interactions received by them from the breeding female. In this same colony, older females and older and heavier males received most of the aggression from the breeding female. The second colony did not show this trend, possibly because it had recently lost many large animals during fighting for succession; in this colony sexual interactions were elevated.

Naked mole-rats Heterocephalus glaber are highly social hystricomorph rodents endemic to the arid regions of East Africa. Living entirely underground, they excavate an extensive system of tunnels with their continuously growing extra-buccal incisors. The majority of the burrow is composed of foraging tunnels, constructed in search of the underground roots and tubers that form their staple diet. Subterranean foraging imposes risks associated with not finding food, and a high energetic cost, and in addition could be limited by the rate of wear of the incisor teeth. The aim of this study was to determine eruption rates for mandibular incisors in naked mole-rats to investigate whether they showed evidence of faster eruption as an adaptation to their subterranean niche and mode of digging. Impeded eruption rates (when the teeth were left in normal occlusion) were initially determined over a period of 1 week in a group of 12 naked mole-rats kept in laboratory conditions. Unimpeded eruption rates were then monitored in the same animals by cutting one mandibular incisor free of occlusion thrice weekly, and measuring growth over a 2-week period. Mean daily impeded eruption rates were c. 228.7±17.5 μm, while mean daily unimpeded rates were higher at c. 624.7±10.4 μm. While impeded eruption rates under laboratory conditions may be an underestimate of the rates occurring in the wild, unimpeded rates (usually about twice the impeded rate) indicate the maximum potential eruption rates of the teeth and are independent of functional activity. These data are not dissimilar from those determined for laboratory rodents and lagomorphs suggesting that the naked mole-rat does not display unusual patterns of eruptive behaviour. Tooth wear resulting from their subterranean lifestyle may be offset as a limiting factor by the social behaviour of the naked mole-rat, where digging activity is distributed among a large workforce during favourable burrowing conditions.

Most naked mole-rats Heterocephalus glaber are countershaded, with purple-grey dorsal but pale pink ventral skin. The exceptions to this coloration pattern are uniformly pink, and include newborn pups, most queens and breeding males, and very old animals. Countershading begins to appear at 2–3 weeks of age and begins to disappear at c. 7 years of age. Countershading may provide camouflage when young naked mole-rats are above ground attempting to disperse. Therefore, reproductives and older workers may lose this coloration once they are unlikely to leave the burrow. Alternative hypotheses for pigmentation that we considered include: thermoregulation, and protection from abrasion or from damaging ultraviolet radiation. These hypotheses are not necessarily mutually exclusive, but do lead to different predictions regarding the development of pigmentation and which colony members should be countershaded.

The lungs of the naked mole-rat Heterocephalus glaber were morphologically (qualitatively) and morphometrically (quantitatively) investigated in adult captive in-burrow body-temperature-maintained (CBTMA) and captive cold-exposed animals (CCEA). The observations were compared with those of field (burrow-dwelling) animals (FA) examined in an earlier study. The lungs of the captive animals were morphologically (qualitatively) similar to those of the field mole-rats. Conspicuous paedomorphic features, i.e. a preponderant double pulmonary capillary arrangement, incomplete differentiation of alveolar pneumocytes, and extension of a cuboidal epithelium to the immediate vicinity of the alveoli, were observed. The prevalent pulmonary underdevelopment was attributed to the relatively low metabolic rate of the poikilothermic naked mole-rat, a species that has evolved in a thermally stable environment. Measurable differences and similarities were found between the lungs of the captive naked mole-rats themselves (i.e. the CBTMA and the CCEA) and between the captive and the field ones. Genetic factors may help explain the conserved pulmonary structural features while environmental (gaseous) change from a hypoxic–hypercapneic (an oxygen deficient–high carbon dioxide concentration) to a normoxic–normocapnic atmosphere and the thermal shift respectively may have enforced pulmonary transformations between the CBTMA and the FA and between the CCEA and the CBTMA. Paradoxically, the CCEA had a significantly lower mass-specific total morphometric pulmonary diffusing capacity of 0.024 compared with that of 0.102 mlO2.s−1.mbar−1.kg−1 in the CBTMA. The observed morphometric differences indicate that the lung of the naked mole-rat, though morphologically unchanged, is intrinsically tractable to environmental shifts in its habitat. Studies on captive naked mole-rats should not be indiscriminately taken to be representative of the species.

The skin structure of 2 Bathyergid rodents, the naked mole-rat (Heterocephalus glaber) and the common mole-rat (Cryptomys hottentotus) is compared, to investigate whether thermoregulatory differences may be attributed to different skin features. Histological and ultrastructural studies of the dorsal skin of these closely related species show morphological and structural similarities but differences in the degree of skin folding, thickness of the integument and dermal infrastructure were evident. The skin of the common mole-rat conforms with expected morphological/histological arrangements that are commonly found in mammalian skin. Many features of the skin of the naked mole-rat, such as the lack of an insulating layer and the loosely folded morphological arrangement contribute to poikilothermic responses to changing temperatures of this mammal. Further evidence for poikilothermy in the naked mole-rat is indicated by the presence of pigment containing cells in the dermis, rather than the epidermis, as commonly occurs in homeotherms. Lack of fur is compensated by a thicker epidermal layer and a marked reduction in sweat glands. Differences in skin morphology thus contribute substantially to the different thermoregulatory abilities of the 2 Bathyergids. The skin morphology is related to the poor thermoinsulatory ability of the animals while simultaneously facilitating heat transfer from the environment to the animal by thigmothermy and/or other behavioural means.

The thermogenic potential of the interscapular brown fat pad in the naked mole-rat Heterocephalus glaber, that exhibits poikilothermic thermal responses to changing temperatures is reported. Histological and ultrastructural study of the brown fat pad showed that it consists of layers of skeletal muscle interposed between the layers of brown adipose tissue with both unilocular and multilocular adipocytes. Large numbers of mitochondria were present between and around the lipid droplets of these cells. Glyoxylic acid condensation, used to demonstrate catecholaminergic nerves, was evident in low concentrations in the connective tissue between the brown adipocytes. A 3-dimensional computer-aided reconstruction of the fat pad showed the extent and ramification of nerves and blood vessels between the adipocytes. These findings show that although the naked mole-rat is regarded as an endothermic poikilotherm, it possesses anatomical features usually found in homeothermic mammals, which are essential for thermogenesis.