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Biomedical subjects

R C Adelman

Publications and source records attributed to R C Adelman.

At least 37 records · Page 2Linked to original sources
PubMed1979

Loss of adaptive mechanisms during aging.

Factors contributing to modifications in the capability for enzyme adaptation as an expression of aging are reviewed. Specific examples of altered enzyme adaptations during aging include the responses of hepatic glucokinase activity to glucose and hepatic tyrosine aminotransferase activity to starvation in Sprague-Dawley rats. These impaired enzyme adaptations apparently are not the consequence of alterations in hepatic function during aging. Instead, they reflect disturbances in extrahepatic hormonal regulatory mechanisms. Specific examples include modifications in the control of circulating levels of insulin glucagon, corticosteroids, and thyroid hormones. Age-dependent changes in the regulation of circulating levels of insulin probably originate within the impaired ability of pancreatic islets of Langerhans to secrete the hormone in response to glucose. The rationale for exploiting this experimental approach as a means to understand biological aging is discussed.

Adaptation, Physiological↗
PubMed1978

Age-associated pathological changes in male rats.

The selection of rats for aging research and the interpretation of experimental results require knowledge of spontaneous age-associated lesions in specific stocks and strains. We have compared selected age-associated pathological changes, as determined by postmortem examination of 113 outbred Crl:CD(SD)BR male retired breeder rats 12--39 months old, with those reported by others in a group of 122 virgin male 12- to 33-month-old F344 rats, an inbred strain from the same commercial source as the outbred rats. Numerous degenerative, inflammatory, and neoplastic lesions occurred in both groups. The wide prevalence and severity of many of the lesions suggest that they could be the source of significant variability in the results of specific aging studies, by their direct and indirect effect(s) on target organs. The prevalence of spontaneous lesions should be defined for each stock or strain intended for use in aging research by postmortem examination of representative groups of animals at various ages. Antemortem diagnostic screening of old rats may also be useful in culling animals bearing lesions that could add to the variability of experimental results, or in selecting for specific lesions that are of research interest themselves.

Aging↗
PubMed1976

A possible role for insulin in the altered capability for hepatic enzyme adaptation during aging.

The pattern of change in the concentration of immunoreactive insulin in portal vein blood during a 7-hour period following intragastric administration of glucose to fasted, male Sprague-Dawley rats is modified both in magnitude and time course of response as rat age increases from 2- to 24-months. This alteration in the control of insulin levels probably is not the consequence of modifications in the availability of administered glucose to the pancreas. A similar modification in the control of insulin secretion also is evident when pancreatic islets isolated from fasted rat donors aged 2- to 24-months are perifused with glucose in vitro. This may represent the first demonstration of an altered response of aging animals which is expressed in the same way in an isolated in vitro system.

Adaptation, Physiological↗
PubMed1975

Impaired hormonal regulation of enzyme activity during aging.

A general feature of all aging populations is the progressively impaired ability to adapt to changes in the surrounding environment. Biochemical expressions of adaptive response include modifications in the rates of enzyme synthesis and degradation, as well as alterations in physiological activity. Therefore, the effects of aging on enzyme adaptation were surveyed in an attempt to explore fundamental biochemical mechanisms in the deterioration of responsiveness. The ability to stimulate adaptive increases in the activity of a large number of enzymes is impared during aging in a variety of tissues from several different species. The impaired capability for liver enzyme adaptation in a rigorously controlled colony of aging male Sprague-Dawley rats probably reflects alterations in hormonal control mechanisms. The present article reviews and evaluates our interest in understanding the effects of aging on regulation of liver enzyme activity by the hormones, insulin and corticosterone. Specific areas currently under investigation include: (1) the regulation of their concentrations in blood; (2) the integrity of their receptor systems in liver; and (3) effectiveness of the endogenous hormone pools fromthe viewpoints fothe availability of physiological antagonists and the potential for alterations in molecular structure.

Adaptation, Biological↗