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G S Roth

Publications and source records attributed to G S Roth.

At least 163 records · Page 9Linked to original sources

Impaired conversion of rat uterine estradiol receptors during aging.

We have examined the effects of aging on the capacity of rat uterine estradiol receptors to be transformed from 8S to 4S and 5S species. Cytosol receptors from mature (6-month-old) rats or senescent (24-month-old) rats have been exposed to various KCl concentrations, ammonium sulfate precipitation and 25 degrees C heating. Estradiol receptors of both the mature and senescent age groups exist in an 8S form on linear 5-20% sucrose gradients in the absence of KCl and are converted to a 4S molecule in the presence of 0.4 M KCl. At intermediate salt concentrations a greater portion of mature receptors was converted to the 4S species. At 0.15 M KCl 62.3% +/- 2.8 of the mature receptors are converted to 4S versus 41% +/- 1.9 of the senescent receptors, and at 0.2 M KCl 79.6% +/- 3.2 of the mature receptors are converted to the 4S versus 58.2% +/- 2.1 of the senescent. Ammonium sulfate treatment in the presence of 0.3 M KCl converted about 80% of the receptors from the 4S to the 5S form, while only about half of the old receptors are affected. When ammonium sulfate precipitates were heated to 25 degrees C all to mature receptors were converted to the 5S species, while only two thirds of the senescent receptors were sedimented at 5S under the same conditions. Inclusion of 20 mM molybdate during preparation blocks conversion of about 15% of the senescent receptors from the 8S to the 4S form but does not affect the mature preparations. Similarly, molybdate treatment does not affect the conversion of the mature estradiol receptors to the 5S form but increases the percentage of senescent receptors remaining in the 4S form from 30 to 45%. Such qualitative differences in receptor conversion may be related to age associated deterioration of estradiol stimulated uterine responsiveness.

Aging↗

Solubilization of striatal D-2 dopamine receptors: evidence that apparent loss during aging is not due to membrane sequestration.

D-2 dopamine receptors from mature (3 to 6 months) and senescent (24 to 25 months) rat striatal membranes were solubilized with the detergent 3-(3-cholamidopropyl) dimethylammonio-2-hydroxy-1-propanesulfonate (CHAPSO). Essentially all of the receptors were recovered following CHAPSO treatment. Approximately 80 to 90% of the receptors were detected in the supernatant fraction under these conditions, with a small percentage remaining membrane bound in both age groups. A 10-fold reduction in binding affinity for [3H]spiperone was observed for solubilized receptors of both age groups. Ultra high speed centrifugation of untreated preparations (200,000 X g) revealed essentially no hidden D-2 dopamine receptors in the light membrane fraction from either mature or senescent rats. These results suggest that a decreased biosynthetic rate (Henry & Roth, 1984; Leff et al., 1984) rather than membrane sequestration accounts for loss of D-2 dopamine receptors with age.

Aging↗

Impaired adrenergic stimulation of rat parotid cell glucose oxidation during aging: the role of calcium.

Adrenergic stimulation of glucose oxidation by epinephrine is reduced by 30 to 40% in isolated rat parotid cell aggregates from aged rats compared with young adults. Such impairment affects both the external calcium dependent and independent components of the response. Age-related differences in glucose oxidation are obliterated if adrenergic receptors are bypassed and stimulation achieved by exposing cells to various concentrations of calcium in the presence of the ionophore, A23187. Thus, impaired calcium mobilization may play, in part, a role in reduced rat parotid adrenergic metabolic responsiveness during aging.

Aging↗

Age-related alterations in the number and function of pituitary lactotropic cells from intact and ovariectomized rats.

We have sought to determine whether the reported age-related increase in in vivo and in vitro PRL secretion in intact and/or postpubertally ovariectomized female rats results from increased number and/or function of lactotropic cells Immunocytochemical staining with antirat-PRL serum, goat antirabbit serum, and peroxidase-antiperoxidase using H2O2 and 4-chloro-1-naphthol or 3'3'-diaminobenzidine hydrochloride as substrates was used to compare the percentages of lactotropes in primary suspensions of heterogeneous adenohypophyseal cells from groups of intact and 3-day ovariectomized mature (6 to 7 month) Wistar rats at estrus (E) or diestrus1-2 (D) with those from the corresponding old (22 to 24 month) rats in constant estrus (CE) or constant diestrus (CD). For both intact and ovariectomized old vs. mature rats, there were small (30-35%) but significant (P less than 0.005) increases in lactotrope number. Lactotrope number did not differ (P greater than 0.05) between E vs. D rats, or CE vs. CD rats, either before or after ovariectomy; moreover, ovariectomy per se did not alter (P greater than 0.05) lactotrope number in any of the groups. Electron microscopic examination of lactotropic cells derived from ovariectomized CE rats revealed ultrastructural changes compatible with estrogenic hyperstimulation; such alterations were not observed in cells from the corresponding E rats. Basal and 17 beta-estradiol (10(-10) M)-stimulated in vitro PRL secretion was measured for 4 days in primary cultures from each of the above groups of rats. After correction for lactotrope number, PRL secretion was greater (P less than 0.01) from cells of intact and ovariectomized CD vs. D rats, whereas 17 beta-estradiol-stimulated (P less than 0.001) but not basal (P greater than 0.05) PRL secretion was greater from the corresponding CE vs. E rats. There was no effect (P greater than 0.05) of reproductive status or of short term ovariectomy on in vitro PRL secretion. These data suggest that aging in the female rat is associated with alterations in both the number and function of pituitary lactotropic cells.

Aging↗

Parathyroid hormone stimulates phosphate efflux through an apparently adenosine 3',5'-monophosphate-independent process in rat parotid cell aggregates.

The effects of PTH on phosphate fluxes and cAMP and protein secretion in rat parotid cell aggregates were studied. PTH-(1-34) as well as PTH-(1-84) stimulated phosphate efflux in a dose-dependent [5 X 10(-7) to 7 X 10(-6) M for human (h) PTH-(1-34), 2 X 10(-7) to 5 X 10(-6) M for bovine (b) PTH-(1-34), and 3.8-114 U/ml for bPTH-(1-84)] and time-dependent [detectable by 15-30 min after incubation with N-terminal PTH and 30-45 min after incubation with bPTH-(1-84)] manner. The effect of PTH on phosphate efflux was saturable, with maximal stimulation at 10(-6) M above for N-terminal PTH and at 57.8 U/ml and above for bPTH-(1-84). Half-maximal stimulation of phosphate efflux by hPTH-(1-34), bPTH-(1-34), and bPTH-(1-84) was achieved at 5.7 X 10(-7) M, 10(-7) M, and 40 U/ml, respectively. Neither bPTH-(1-34) nor bPTH-(1-84) had any effect on phosphate uptake by parotid cell aggregates at the concentrations examined. bPTH-(1-34) and bPTH-(1-84) also stimulated amylase secretion, with a significant increase in cAMP production (70-90% over basal). However, (BU)2cAMP did not stimulate phosphate efflux. Isoproterenol (10(-5) M) markedly stimulated cAMP production and amylase secretion without causing a significant increase in phosphate efflux. Oxidized bPTH-(1-84) and the C-terminal fragment of hPTH had no stimulating effect on phosphate efflux. The present results suggest, therefore, that PTH may play an important role in regulating rat parotid cell phosphate metabolism through an apparently cAMP-independent process.

Amylases↗

Effects of aging on mechanisms of alpha-adrenergic and dopaminergic action.

Mammalian parotid glands have provided excellent model systems for studying adrenergic control of defined biochemical and physiological processes during exocrine secretion. The findings point to a deficiency in a key coupling step (postulated here to exist just distal to the alpha 1-adrenergic receptor yet proximal to the phospholipid turnover/Ca2+ mobilization steps) required for alpha-adrenergic-mediated fluid and electrolyte secretion from the aging rat exocrine parotid gland. Because the steps involved in this process are not fully elucidated, natural perturbation of rat parotid gland function should prove to be of particular value as a model toward clarification of the mechanisms of alpha-adrenergic signal transduction. It is now generally agreed that dopamine receptors are lost from the corpus striatum during aging in a variety of species, including humans. Most studies of age changes in striatal dopamine receptors have detected no alterations in binding affinity or dissociation constant (Kd). Only reduction in concentration (Bmax) with increasing age is apparent. Such receptor loss appears to be at least partially responsible for decreased dopamine stimulation of certain stereotypic behavioral responses and decreased neurotransmitter release. In addition, dopamine-sensitive adenylate cyclase (EC 4.6.1.1) decreases during senescence.

Aging↗

Adrenergic-agonist-induced Ca2+ fluxes in rat parotid cells are not Na+-dependent.

We investigated the hypothesis that extracellular Na+ is required for the rapid mobilization of Ca2+ by rat parotid cells after adrenergic stimulation. When Na+ salts in the media were osmotically replaced with either choline chloride (+atropine) or sucrose, efflux of 45Ca2+ from preloaded cells, caused by 10 microM-(-)-adrenaline, was unchanged. Similarly adrenaline stimulated 45Ca2+ uptake into cells under nonsteady-state conditions in the presence or absence of Na+. Monensin, a Na+ ionophore, was able to elicit a modest increase in 45Ca2+ efflux, compared with controls. Studies of net 45Ca2+ flux, performed under near-steady-state conditions, showed that adrenaline caused net 45Ca2+ accumulation, whereas monensin caused net 45Ca2+ release. The effect of monensin required the presence of Na+ in the incubation medium. Both 1 mM-LaCl3 and 0.1 mM-D-600 prevented adrenaline-stimulated 45Ca2+ uptake into cells, but had no effect on monensin-induced changes. We conclude that (1) the rapid mobilization of Ca2+ by adrenergic agonists seen in rat parotid cells does not require a Na+out greater than Na+in gradient and (2) the nature of the monensin effect is quite different from the adrenergic-agonist-induced response.

Animals↗

Decreased estrogenic stimulation of RNA polymerase II in aged rat uteri is apparently due to reduced nuclear binding of receptor-estradiol complexes.

The maximum ability of receptor-estradiol complexes to activate RNA polymerase II and bind to nuclear acceptor sites is reduced 40-50% in senescent rat uteri. A precise, linear stoichiometric relationship exists between acceptor site occupancy and polymerase activity, and this relationship is not altered with aging. Thus, reduced ability of estrogen to stimulate RNA polymerase II in aged rat uteri appears to be due to deficits in binding of receptor-estradiol complexes to nuclear acceptor sites.

Aging↗

Stimulation of glucose oxidation in rat submandibular gland cells in vitro by analogues of cyclic AMP.

Secretion from salivary glands, following autonomic stimulation, is energy-dependent. Rat submandibular gland cells, when treated in vitro with both alpha- and beta-adrenergic agonists, showed increased glucose oxidation. The effects of alpha-adrenergic agents on glucose metabolism can be mimicked by non-receptor mobilization of Ca2+. Analogues of cyclic AMP were capable of elevating glucose metabolism to nearly the same extent as beta-adrenergic agonists.

Animals↗

Effects of aging on the lipid order and composition of rat adipocyte ghosts.

An analysis of the cholesterol/phospholipid ratio of adipocyte ghosts from rat epididymal fat pads shows a significant increase with age (P less than 0.005). An attempt to correlate these changes with the order of the lipid matrix was made using the stearic acid spin label 2-(3-carboxypropyl)-4, 4-dimethyl-2-tridecyl-3-oxazolidinyloxyl [I(12,3)]. Although order was negatively correlated with temperature in preparations from both 6- and 24-month-old rats, no effect of age could be detected.

Adipose Tissue↗

Alpha 1-adrenergic responsiveness of young adult and aged rat submandibular cells in vitro.

The present study has evaluated, in vitro, alpha 1-adrenergic receptor mediated responses in submandibular cells from young adult and aged rats. Submandibular glands from different aged rats possess a similar number of alpha 1-adrenergic receptors that display comparable binding characteristics. Following alpha 1-adrenergic stimulation, cells from both groups of rats show a similar ability to mobilize intracellular Ca2+ (45Ca2+ time course, agonist dose-response) and to elicit a functional response (inhibition of protein synthesis by epinephrine) which reflects Ca2+ mobilization.

Aging↗

Age-associated changes in nuclear binding of rat uterine estradiol receptor complexes.

Nuclear binding of cytoplasmic estrogen receptors was measured in an in vitro cell-free system, using various mixtures of cytosols and nuclei from uteri of mature (6-9 month old) and senescent (24-25 month old) Wistar rats. Both nuclei and cytoplasmic receptors from senescent uteri were 25-35% less efficient in supporting nuclear binding than those obtained from mature tissues as evidenced by the concentrations of occupiable nuclear acceptor sites. No age differences in association or dissociation constants were observed for the nuclear binding reaction. However, the apparent inability of some aged receptors to bind to the full complement of mature nuclear acceptor sites may indicate a qualitative deficiency in the cytosols of senescent uteri.

Aging↗

Effect of aging on recovery of striatal dopamine receptors following N-ethoxycarbonyl-2-ethoxy-1, 2-dihydroquinoline (EEDQ) blockade.

The recovery rate of striatal dopamine receptors following blockade by N-ethoxycarbonyl-2-ethoxy-1, 2-dihydroquinoline (EEDQ) in vivo is reduced by 25-35% in striata from senescent Wistar rats when compared to mature counterparts. No differences in binding affinity for [3H]-spiperone were observed for the different age groups at various times after EEDQ injection. These results suggest that loss of striatal dopamine receptors during aging may be due to a decreased biosynthetic rate.

Aging↗

Delayed loss of striatal dopamine receptors during aging of dietarily restricted rats.

Dietary restriction by feeding every other day retards the normal age-associated loss of dopamine receptors from the corpus striatum of the rat. Ad libitum fed animals lose about 40% of the receptors labeled by [3H]spiperone between 3 and 24 months, while the loss is only about 20% over the same period in restricted rats. Ultimately, by 30 months of age, values for restricted animals drop to those of 24-month-old ad libitum-fed rats. The mean lifespan of restricted rats, however, is about 40% longer than the 22-24 months characteristic of ad libitum-fed counterparts. The effect of restriction appears to be chronic rather than acute since ad libitum-fed rats which are restricted for 2 weeks prior to sacrifice possess receptor levels comparable to 24-month-old rats maintained on ad libitum feeding for their entire lifetime.

Age Factors↗

Isolated uterine nuclei and cytosol receptors of aged rats exhibit impaired estrogenic stimulation of RNA polymerase II.

An in vitro cell-free system of uterine nuclei and cytosol receptors has been used to analyze the effects of aging on estrogen stimulation of RNA polymerase II activity. By using fixed concentrations of nuclei and cytoplasmic receptor--estrogen complexes (R-E2), it was found that mature nuclei are 3 times more efficient (155% vs. 57%) than old ones for stimulation of polymerase activity by mature R-E2. Meanwhile, mature R-E2 are 5 times more efficient (155% vs. 31%) than old ones in supporting such stimulation in mature nuclei. Stimulation by old cytosol R-E2 is so poor that it is essentially unaffected by nuclear age (31% with both mature and old nuclei). Finally, equimolar mixtures of mature and old cytosol R-E2 stimulate polymerase II activity in mature nuclei by 77%, a value intermediate between mature and old cytosols used separately. These results indicate that both nuclei and cytosol from old uteri are deficient in their ability to support estrogenic stimulation of RNA polymerase II.

Aging↗

Excess in vitro prolactin secretion by pituitary cells from ovariectomized old rats.

Various in vivo and in vitro pituitary lactotropic and gonadotropic functions were measured in mature (6-7 mo, normally cycling) and old (24 mo, constant diestrus) female Wistar rats. Serum prolactin (PRL) levels were higher (P less than 0.001), whereas luteinizing hormone (LH) values were similar (P greater than 0.05) in old versus mature rats both before and 3 days after ovariectomy. Serum PRL levels decreased significantly (P less than 0.005) postovariectomy only in the mature rats. The in vitro release of PRL and LH was measured for 4 days in primary adenohypophyseal cell cultures from the ovariectomized rats. Both basal and 17 beta-estradiol (E2)-stimulated PRL release (P less than 0.001) and production (P less than 0.005) were greater by cells from old rats. In contrast, both basal release and E2-stimulated LH release were greater (P less than 0.001) by cells from mature rats. Peak PRL release by cells from both old and mature rats occurred after exposure to E2 doses 1/100th of those required for peak LH release. These data support the hypothesis that intrinsic derangements in anterior pituitary function contribute to the reproductive decline in aging female rats and that different pituitary cell types exhibit discordant age changes in estrogenic sensitivity.

Aging↗

Effects of in vivo estradiol administration on availability of rat uterine nuclear acceptor in measured in vitro.

Estradiol injected in vivo successfully completes for binding to uterine nuclear acceptor sites measured by the assay of Kon and Spelsberg (1). Such competition is time-and dose-dependent, with maximal inhibition (75%) 1 h after injection and at a dose of 10 micrograms of 17 beta-estradiol per 300 g of BW. Thus, this assay appears to accurately measure those uterine nuclear acceptor sites mediating estrogen action in vivo.

Animals↗