Differential effects of thyrotropin-releasing hormone on in vitro release of in vivo or in vitro newly synthesized and mature prolactin by lactating rat adenohypophyses. Further evidence for a sequential pattern of hormone release.

We studied the basal and thyrotropin-releasing hormone (TRH)-stimulated in vitro release of newly synthesized and mature prolactin (PRL) by lactating rat pituitary fragments. Newly synthesized PRL was defined as that resulting from either in vivo pulse labelling with [3H]-leucine (injected i.v. 10 min before removing the pituitary glands for in vitro incubation); or in vitro labelled by a 5-min preincubation period of adenohypophyseal fragments. Mature PRL was defined as that labelled in vivo 8 h before incubation. Medium PRL was quantified by polyacrylamide-gel-electrophoresis densitometric and liquid scintillation techniques. Under basal conditions, both total (unlabelled) and 8-hour labelled (mature) PRLs showed an in vitro release pattern characterized by an initial period of faster and higher secretion that lasted for 30-60 min followed by a lower secretion rate that extended from 60 to 240 min of incubation. Secretion of newly synthesized PRLs was detected since the first 30 min, but did not reach maximum levels until 90-120 min of incubation. Accordingly, PRL release during the first 30-60 min of incubation consisted primarily of mature PRL, whereas secretion during the rest of incubation included the release of newly synthesized hormone. These results confirm previous data on the sequential, rather than preferential, release of different age PRLs. TRH (0.35 microM) stimulated (about 30% above control) the release of both total and mature PRLs. No effect could be detected upon the release of in vivo labelled new PRL, while the same dose of TRH strongly stimulated (about 100% above control) the release of in vitro labelled new PRL.(ABSTRACT TRUNCATED AT 250 WORDS)

Investigation into the role of dopamine and lysosomes in the impairment of prolactin transformation and release imposed by long periods of non-suckling in the rat.

The transformation of prolactin (PRL) within lactating rat hemipituitary glands incubated for 240 min and the release of the hormone into the incubation medium were progressively reduced by dopamine added to the medium over a 2.3-49 mumol/l range of concentration; the antilysosomal drug chloroquine did not alter these effects of dopamine. In related experiments, the short-term action of dopamine was manifested also upon in vitro transformation, repletion and release of in vivo labelled [3H]PRL, thus indicating that dopamine inhibits all phases of PRL secretion by the lactating rat anterior pituitary (AP). In other experiments, increasing the non-suckling period from 8 to 16 h reduced the pre-suckled concentration of PRL in the lactating rat AP, reduced the ability of the AP to transform PRL in response to suckling, and reduced the capability of the AP of such rats to secrete PRL in vitro. Injecting chloroquine (0.2 mmol/kg ip), haloperidol (0.27 mumol/kg ip) or providing 15-30 min of suckling midway during the 16-h non-suckling period restored each of these functions. Thus, frequent uncoupling of dopamine from its receptor appears necessary to prevent impairment of the suckling-induced transformation mechanism in the lactating rat AP and, presumably, to prevent PRL in the lactotrope from reaching an age where it becomes susceptible to lysosomal degradation.

Reversal by thiols of dopamine-, stalk-median eminence-, and zinc-induced inhibition of prolactin transformation in adenohypophyses of lactating rats.

Depletion-transformation of PRL is a decrease in tissue PRL detectability which precedes and may often be required for increased PRL release. The present studies were designed to determine whether thiol-disulfide interchange mechanisms may be involved in PRL transformation and release by the pituitary of the lactating rat. Thirds of 8-h nonsuckled lactating rat adenohypophyses were incubated with or without thiols (reduced glutathione, the aminothiol cysteamine, or mercaptoethanol), in the presence of known inhibitors of transformation and release such as dopamine (DA), stalk median eminence (SME) extract, or Zn++. PRL concentrations in pre- and postincubated tissues, as well as the amount of released PRL, were determined by polyacrylamide gel electrophoresis and densitometry. In 30-min incubations without additions, 12-22% of the tissue PRL was depleted; however, in the presence of 17-50 microM DA, all doses of SME extracts tested (0.5-2.0 eq), or 0.1 mM Zn++, depletion was partially or totally prevented and PRL release was inhibited 25-60%. On the other hand, when thiols were added in addition to the above agents, a complete, dose-related, restoration of PRL depletion was obtained. In 120-min incubations, thiols similarly reversed the effects of 0.05 mM DA on depletion, but thiols did not reverse the inhibition of PRL release caused by DA, SME, or Zn++. Other data indicate that thiols alone may inhibit rat PRL release and also facilitate or induce PRL depletion; in bovine PRL granules, thiols reverse Zn++ inhibition of PRL release and detectability. These data suggest that thiol-disulfide interchange reactions may be importantly involved in both depletion-transformation and in secretion. The precise thiol sensitivity of the two processes does not appear identical, secretion being more sensitive to DA and less sensitive to thiols than depletion-transformation.

Thiol regulation of depletion-transformation and release of prolactin by the pituitary of the lactating rat.

We investigated the possibility that thiol-disulfide interchange mechanisms are involved in depletion-transformation (loss of tissue PRL detectability) and release of PRL from adenohypophyses (AP) of lactating rats. The influence of pH, bicarbonate, and Triton X-100 as well as thiol-related compounds on these processes was assessed. Tissue PRL was depleted-transformed by the use of three different conditions: 1) 30 min of suckling after 8 h of nonsuckling; 2) in vitro incubation of APs for 2 h; or 3) in vivo cysteamine (CSH) treatment. Lactating rats nonsuckled for 8 h served as controls (no depletion-transformation). The depletion-transformation phenomenon was unchanged by extraction with Tris-HCl-0.1% Triton X-100 buffers but reversed either by extraction with bicarbonate buffer (pH 8.2 or 9.7) or by incubation of pH 8.2 homogenates for 3 h at 37 C. Reduced glutathione (GSH) added to these homogenates further enhanced PRL detectability. At pH 6.5, however, incubation with or without GSH had the opposite effect and decreased PRL detectability. In AP incubations, depletion was increased in a dose- and time-dependent fashion by the aminothiol CSH, and by GSH, dithiothreitol, or mercaptoethanol but not sodium ascorbate. These agents also inhibited PRL release. Similar results were obtained after injection of CSH (20-120 mg/kg BW) 4 h before death. Depletion and release of PRL in incubated APs were prevented by iodoacetamide and N-ethylmaleimide (0.1-5 mM); GSH or CSH counteracted these effects. In contrast to the alkylating agents, oxidized glutathione and 5,5'-dithio-2-nitrobenzoic acid inhibited PRL depletion but stimulated PRL release. Thus, thiols and aminothiols may preferentially lead to depletion-transformation of PRL, whereas disulfides may inhibit depletion and facilitate PRL release. Although in some experiments increased depletion was dissociated from increased release, nonetheless the data support the concept that shifts in PRL detectability during depletion-transformation, repletion, and release involve thiol-disulfide interchange mechanisms.

Release of catecholamines follows suckling or electrical stimulation of mammary nerve in lactating rats.

The hypothesis that catecholamines may be released by mammary gland stimulation during lactation was tested by measuring, with an HPLC electrochemical method, plasma epinephrine (E) and norepinephrine (NE) concentrations during suckling in conscious rats and during electrical stimulation (pulses: 1 msec duration, 10/sec at 5-30 V) of the central end of a cut abdominal mammary nerve in urethane-anesthetized rats. Plasma E and NE concentrations were significantly elevated in two different strains of rats (Wistar and Holtzman) within 5 min of suckling. The concentration of E and NE did not change in control unsuckled rats during the same time period. As a complementary indication of sympathetic activation, it was observed that piloerection occurred during suckling. Plasma E levels (but not NE levels) increased significantly within 30 sec of a 2-min period of nerve stimulation in lactating rats on either day 7 or day 21 of lactation, as well as in nonlactating rats. The effect was significantly greater in nonlactating rats. The levels of E and NE were not altered after sham stimulation, whereas adrenalectomy abolished the rise in plasma E after mammary nerve stimulation. Blockade of the rise in plasma E also occurred after rapid injection of 100 microliters milk intraductally into each of two thoracic mammary glands, 15 sec before the onset of mammary nerve stimulation. These results show that E and NE can be released in response to suckling, and that activation of ductal mechanoreceptors may inhibit such release. These mechanisms may operate to regulate the rate of milk removal during suckling in the rat.

In-vivo and in-vitro secretion of prolactin by lactating rat adenohypophyses as a function of intracellular age.

Adenohypophysial prolactin of lactating rats was pulse-labelled by [3H]leucine injected i.v. at the time of removal of the pups. The [3H]prolactin concentration in the pituitary gland, analysed by polyacrylamide-gel electrophoresis, progressively fell as the time from labelling to removal of the pituitary gland increased from 8 to 24h, which suggests that there was a loss of hormone as it aged within the gland. Suckling effectively provoked the depletion-transformation of total and [3H]prolactin (extracted at pH 7.2) when applied after 8 h but not when applied after either 16 or 24 h after removing the pups. In rats whose pups were removed for 8 h, suckling also depleted-transformed [3H]prolactin labelled 4 h, but not that labelled 1 h before suckling. The pituitary glands of other lactating rats were labelled with [3H]leucine injected i.v. at various times before removing the glands and incubating them in medium 199. The secretion into the medium of [3H]prolactin labelled either 4, 8, 16 or 24 h beforehand was maximal during the first 30 min then declined from 30 to 240 min of incubation. However, secretion of prolactin labelled 1 h and 10 min beforehand reached a maximum after 0.5-1 h and 2 h of incubation respectively, then remained constant during the remainder of the 4-h incubation period. The total 4-h secretion of [3H]prolactin was greatest (65% of preincubation concentration) from those glands labelled 4 h before in contrast to those labelled 10 min (15%) or 1 (38%), 8 (34%), 16 (18%) or 24 h (26%) before incubation.(ABSTRACT TRUNCATED AT 250 WORDS)

Latency and duration of the effects of bromocriptine and prolactin on milk secretion in lactating rabbits.

Milk yields were measured at 8h intervals in rabbits during early (days 11-14) and late (days 31-34) lactation. A single injection of 1 mg bromocriptine given to rabbits 30 min before sucking on days 11 or 31 caused a significant reduction in milk yield after approximately 8h. The depressant effect of the drug was then maintained over the next 24-36h. Recover of milk yield occurred in bromocriptine-treated rabbits during both early and late lactations 8-16h after a single injection of 3 mg prolactin. The recovery accelerated more in the rabbits in the early lactating group. Attainment of the maximal stimulatory effect occurred by 24h after prolactin injection during both early and late lactation although the improvement in milk yield lasted for a shorter period (8h compared with 24h) during late lactation compared with early lactation. These differences in response of the rabbit to prolactin during late lactation may contribute substantially to the declining milk yields characteristic of late lactation in this species.