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1.
Rehabilitation (Stuttg) ; 52(5): 329-36, 2013 Oct.
Article in German | MEDLINE | ID: mdl-23749615

ABSTRACT

AIM OF THE STUDY: We evaluated an occupation-related rehabilitation program, which has been designed to enhance the return to work of cancer patients. As return to work plays an important role to get back to normalcy after suffering from cancer, there is a substantial need for support and evaluated programs. METHODS: The study had a quasi-experimental design with an intervention group (IG) and a comparison group (CG). We defined performance-related outcomes (e. g. return to work, self-assessed working capacity), asked patients if they needed further vocational advice and how helpful they estimated the rehabilitation treatment. 1 year after the end of rehabilitation 309 employed patients had completed the study (65%). We addressed our research questions using non-parametric tests, t-tests, analyses of variance and logistic regressions. RESULTS: Of the 309 patients 58% started rehabilitation not later than 14 days after the end of acute treatment while the other 42% had finished their treatments at least some weeks or even months ago. Patients of the IG evaluated the work-related rehabilitation offers significantly better and needed less additional vocational advice after the end of rehabilitation (n. s.). Regarding the patients, who started rehabilitation not later than 14 days after the end of acute treatment (beginning of rehabilitation n=269, 12 months after rehabilitation n=174), the IG achieved a slightly higher return-to-work-rate 12 months after the end of rehabilitation (81% IG, 76% CG, n. s.). Above that the IG estimated their subjective working capacity significantly more often as fully re-established (IG 46%; CG 29%, p=0,030). CONCLUSIONS: A high percentage of the patients return to work (78%). These results show the success of oncological rehabilitation in helping patients to return to work. In addition, the occupation-related rehabilitation program enhances subjective variables as the satisfaction of the patients regarding the information and the improvement of the patients' working-capacity.


Subject(s)
Hospitalization/statistics & numerical data , Neoplasms/epidemiology , Neoplasms/rehabilitation , Rehabilitation, Vocational/methods , Return to Work/statistics & numerical data , Unemployment/statistics & numerical data , Work Capacity Evaluation , Female , Germany/epidemiology , Humans , Male , Medical Oncology/statistics & numerical data , Middle Aged , Outcome Assessment, Health Care/methods , Prevalence , Prognosis , Program Evaluation , Rehabilitation, Vocational/statistics & numerical data , Risk Factors , Treatment Outcome
2.
J Cancer Res Clin Oncol ; 123(11-12): 632-8, 1997.
Article in English | MEDLINE | ID: mdl-9620222

ABSTRACT

Intercellular adhesion molecule-1 (ICAM-1) expression correlates with tumour progression in patients with malignant melanoma or renal cell carcinoma. To assess the value of soluble ICAM-1 (sICAM-1) for lung cancer patients, sICAM-1 was determined by means of an enzyme-linked immunosorbent assay. Sera from 147 patients with lung cancer, from 75 patients with benign lung diseases and from 108 healthy adults were investigated for sICAM-1 expression. Significant differences in sICAM-1 levels were detected in lung cancer patients (387 +/- 176 ng/ml) and patients with benign lung diseases (365 +/- 110 ng/ml) compared to the group of healthy adults (310 +/- 90 ng/ml). There was no difference in sICAM-1 level among the subtypes of lung cancer. Advanced tumour stages and patients with progressive disease tended to be associated with higher sICAM-1 levels, the site of metastasis being relevant for the level attained. Patients with liver metastasis had the highest sICAM-1 levels (547 +/- 295 ng/ml) compared to patients with cerebral metastasis (317.8 +/- 92.2 ng/ml). An increase of sICAM-1 expression during the progression of the disease coincided with a poorer survival prognosis for the patients compared to patients with stable or falling sICAM-1 levels.


Subject(s)
Intercellular Adhesion Molecule-1/blood , Lung Diseases/blood , Lung Neoplasms/blood , Adolescent , Adult , Aged , Biomarkers, Tumor/blood , Disease Progression , Female , Humans , Lung Neoplasms/mortality , Male , Middle Aged , Survival Rate
3.
Eur J Cancer ; 29A(16): 2250-5, 1993.
Article in English | MEDLINE | ID: mdl-8110495

ABSTRACT

Ten small cell lung carcinoma and 12 non-small cell lung carcinoma cell lines of various histological types were studied for constitutive expression of the intercellular adhesion molecule-1 (ICAM-1). ICAM-1 was present in all squamous and large cell carcinoma cell lines whereas two out of five adenocarcinoma and all small cell lung cancer (SCLC) cell lines showed no basal ICAM-1 expression. ICAM-1 expression was upregulated by tumour necrosis factor-alpha (TNF-alpha) in a time- and dose-dependent manner in cell lines with basal ICAM-1 expression. Western blot analysis revealed a molecular size of 85 kDa for ICAM-1 in all but one cell line. The TNF-alpha-induced upregulation of ICAM-1 occurs on the transcriptional level. Adhesion of peripheral blood mononuclear cells to lung tumour cell lines could be inhibited by monoclonal antibodies (MAb) (CD11a;CD18) against the receptor of ICAM-1, the leukocyte function-associated antigen-1 (LFA-1), but not by a MAb (CD54) against ICAM-1 itself.


Subject(s)
Cell Adhesion Molecules/biosynthesis , Lung Neoplasms/metabolism , Blotting, Northern , Blotting, Western , Carcinoma, Non-Small-Cell Lung/metabolism , Carcinoma, Small Cell/metabolism , Cell Adhesion , Dose-Response Relationship, Drug , Humans , Tumor Cells, Cultured , Tumor Necrosis Factor-alpha/pharmacology , Up-Regulation
4.
Exp Cell Res ; 204(1): 22-9, 1993 Jan.
Article in English | MEDLINE | ID: mdl-8380141

ABSTRACT

Small cell lung cancer (SCLC) cell lines were investigated for the expression of insulin-like growth factor (IGF) II receptor by means of radioreceptor assays, cross-linking techniques, and Northern blot analysis. 125I-IGF II binds to both the IGF I and the IGF II receptor on intact SCLC cells. Detailed receptor assays performed on microsomal and plasma membranes gave evidence that 125I-IGF II binds with high affinity (70-80 pM) to the IGF I receptor and with low affinity (2-4 nM) to the IGF II receptor, and not conversely. The presence of mannose-6-phosphate enhanced the binding of 125I-IGF II to the IGF II receptor of SCLC. Mannose-6-phosphate also increased the efficiency of N-hydroxysuccinimide ester in cross-linking 125I-IGF II to the IGF II receptor and facilitated the cross-linking of 125I-IGF II to a second protein of 240-250 kDa. Soluble IGF II receptor was also detected in conditioned media of SCLC cell lines.


Subject(s)
Carcinoma, Small Cell/metabolism , Lung Neoplasms/metabolism , Receptor, IGF Type 2/metabolism , Blotting, Northern , Cell Membrane/metabolism , Cross-Linking Reagents , Culture Media, Conditioned , Humans , Insulin-Like Growth Factor I/metabolism , Intracellular Membranes/metabolism , Microsomes/ultrastructure , Radioligand Assay , Tumor Cells, Cultured
5.
J Cancer Res Clin Oncol ; 118(7): 502-8, 1992.
Article in English | MEDLINE | ID: mdl-1320623

ABSTRACT

Small-cell lung cancer (SCLC) and non-small-cell lung cancer (NSCLC) cell lines were studied for insulin-like growth factor I (IGF-I) receptor expression and with regard to the influence of IGF-I on cell proliferation. IGF-I receptors on the cells were characterized by competitive binding assays, chemical crosslinking and northern blot hybridization of IGF-I receptor mRNA. All SCLC and NSCLC cell lines showed specific IGF-I binding sites with an affinity (KD) of 0.69-5.21 nM. The amount of binding sites ranged from 59 fmol/mg to 1230 fmol/mg protein. The IGF-I binding was inhibited by the IGF-I receptor antibody (alpha-IR-3). Northern blot hybridization indicated that IGF-I receptor mRNA was being produced by all SCLC and NSCLC cell lines. We used the soft-agarose clonogenic assay to evaluate the influence of IGF-I on the in vitro proliferation of the cells. Our results have shown that IGF-I stimulates the growth of all tested cell lines ranging from a factor of 1.6 to 4.2 in SCLC and from 1.1 to 2.7 in NSCLC. The data indicate that the IGF-I receptor thus appears to be the common pathway for the mitogenic activity of IGF-I and IGF-II with regard to human lung cancer cells.


Subject(s)
Carcinoma, Non-Small-Cell Lung/metabolism , Carcinoma, Small Cell/metabolism , Insulin-Like Growth Factor I/metabolism , Lung Neoplasms/metabolism , Receptors, Cell Surface/metabolism , Binding, Competitive , Blotting, Northern , Carcinoma, Non-Small-Cell Lung/pathology , Carcinoma, Small Cell/pathology , Cell Division/drug effects , Humans , Insulin-Like Growth Factor I/pharmacology , Lung Neoplasms/pathology , Radioligand Assay , Receptors, Somatomedin , Tumor Cells, Cultured
6.
J Steroid Biochem Mol Biol ; 37(6): 877-82, 1990 Dec 20.
Article in English | MEDLINE | ID: mdl-2178366

ABSTRACT

Lung cancer is a major health problem, with over 38,000 new cases expected every year in West Germany. A more complete understanding of the biology of lung cancer will hopefully lead to therapeutic modalities. The possible autocrine growth regulation in small-cell lung cancer and non-small-cell lung cancer has been demonstrated for bombesin/GRP, vasopressin, neurotensin, EGF/TGF alpha, transferrin-related peptides and insulin-like growth factors. This contribution concentrates on recent data concerning binding sites, growth promoting effects and secretion of IGFs in lung cancer cell lines. The production of IGF-binding proteins which were also produced by lung cancer cell lines modifies the autocrine/paracrine model for IGFs since then proteins can either enhance or inhibit the effect of IGFs on tumor growth.


Subject(s)
Lung Neoplasms/metabolism , Receptors, Cell Surface/metabolism , Somatomedins/metabolism , Humans , Insulin-Like Growth Factor II/genetics , Receptors, Somatomedin , Somatomedins/genetics , Tumor Cells, Cultured
7.
FEBS Lett ; 267(2): 295-300, 1990 Jul 16.
Article in English | MEDLINE | ID: mdl-2165922

ABSTRACT

Immunocytochemical and immunochemical techniques were used to study the expression of the neural cell adhesion molecule (NCAM) by human lung cancer cell lines. Intense surface staining for NCAM was found at light and electron microscopic levels on small cell lung cancer cells. The NCAM polypeptide of Mr 140,000 (NCAM 140) was detected by immunoblotting in all of 7 small cell lung cancer cell lines examined and in one out of two of the closely related large cell cancer cell lines: it was not detected in cell lines obtained from one patient with a mesothelioma, in two cases of adenocarcinoma, nor in two cases of squamous cell cancer. In contrast, neuron-specific enolase was found by immunoblotting in all the lung cancer cell lines tested and synaptophysin in all but the adenocarcinoma cell lines. These antigens were localized intracellularly. The specific expression of NCAM 140 by human small and large cell lung carcinomas suggests its potential as a diagnostic marker.


Subject(s)
Biomarkers, Tumor/analysis , Carcinoma, Small Cell/analysis , Cell Adhesion Molecules, Neuronal/analysis , Lung Neoplasms/analysis , Cell Adhesion Molecules, Neuronal/ultrastructure , Humans , Immunoenzyme Techniques , Microscopy, Electron , Tumor Cells, Cultured
8.
Exp Cell Res ; 184(2): 396-406, 1989 Oct.
Article in English | MEDLINE | ID: mdl-2553455

ABSTRACT

Conditioned serum-free media (CM) from small-cell lung cancer (SCLC) cell lines were examined for the presence of insulin-like growth-factor-binding proteins (IGF-BP). 6/9 SCLC cell lines secreted binding proteins with high affinity for IGFs. When [125I]IGF-I or [125I]IGF-II was incubated with the CMs, complexes of tracer with proteins could be demonstrated by gel filtration, by precipitation with polyethylenglycol, and after adsorption of unbound tracer with activated charcoal. Analysis of binding data according to the method of Scatchard resulted in linear plots for IGF-I and IGF-II. The dissociation constants were determined to be 0.106 nM for IGF-I and 0.209 nM for IGF-II binding. Cross-linking of [125I]IGF-I or [125I]IGF-II to the CMs followed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) under nonreducing conditions revealed the presence of IGF-BPs with molecular masses in the range 24-32 kDa. The binding was competitively inhibited by addition of cold IGF-I and IGF-II but not by insulin. Northern blot hybridization with an IGF-BP cDNA probe encoding a low-molecular-weight IGF-BP from a human placenta cDNA library and Western blot analysis with a corresponding polyclonal antibody showed no expression of this gene. These data demonstrate that SCLC cell lines release IGF-BPs in culture supernatants, which differ from IGF-BPs detected in liver and placenta. These IGF-BPs might be important mediators in the autocrine/paracrine growth regulation of IGFs in SCLC.


Subject(s)
Carcinoma, Small Cell/metabolism , Insulin-Like Growth Factor II/metabolism , Insulin-Like Growth Factor I/metabolism , Lung Neoplasms/metabolism , Somatomedins/metabolism , Carcinoma, Small Cell/pathology , Cell Line , Electrophoresis, Polyacrylamide Gel , Humans , Immunoblotting , Lung Neoplasms/pathology , Tumor Cells, Cultured/metabolism , Tumor Cells, Cultured/pathology
9.
Int J Cancer ; 43(4): 685-91, 1989 Apr 15.
Article in English | MEDLINE | ID: mdl-2539332

ABSTRACT

We investigated the influence of testosterone on binding to established small-cell lung cancer (SCLC) cell lines and were able to show specific high-affinity and low-capacity binding sites in some cell lines with a typical receptor size, using sucrose density gradient centrifugation. In addition, we demonstrated marked growth stimulation with testosterone and dehydrotestosterone using different androgen-receptor-positive small-cell lung cancer cell lines. This growth stimulation could be counteracted by the addition of anti-androgens like cyproterone acetate or flutamide. The presence of 5 alpha-reductase activity, 17 beta-hydroxysteroid-dehydrogenase and 3 alpha-hydroxysteroid-dehydrogenase activities could be demonstrated, suggesting testosterone metabolism of small-cell lung cancer cell lines.


Subject(s)
Androgens/pharmacology , Carcinoma, Small Cell/metabolism , Lung Neoplasms/metabolism , Oxidoreductases/metabolism , Receptors, Androgen/metabolism , Androgen Antagonists/pharmacology , Androgens/metabolism , Carcinoma, Small Cell/pathology , Cell Division/drug effects , Cell Line , Centrifugation, Density Gradient , Cholestenone 5 alpha-Reductase , Dose-Response Relationship, Drug , Humans , Lung Neoplasms/pathology , Oxidoreductases/analysis , Radioligand Assay , Receptors, Androgen/drug effects , Thymidine/metabolism , Tritium , Tumor Cells, Cultured
10.
Peptides ; 9(6): 1367-72, 1988.
Article in English | MEDLINE | ID: mdl-2470067

ABSTRACT

Human small cell lung cancer (SCLC) produces and secretes BN/GRP (bombesin/gastrin releasing peptide). Because BN stimulates the growth of SCLC cells and these cells have receptors for BN-like peptides, it is important to define agents which disrupt this self-promoting autocrine growth cycle. Here, substance P analogues were evaluated as BN receptor antagonists using SCLC cell lines. (D-Arg1, D-Pro2, D-Trp7.9, Leu11) substance P [(APTTL)SP] was one of the more potent analogues tested in inhibiting BN-like peptide receptor binding with an IC50 value of 1 microM. Micromolar concentrations of (APTTL)SP antagonized BN receptor mediated elevation of cytosolic Ca2+ levels and decreased the colony formation in soft agarose. These data suggest that SP analogues function as SCLC BN receptor antagonists and may be useful in disrupting the autocrine growth function of BN-like peptides.


Subject(s)
Receptors, Neurotransmitter/drug effects , Substance P/analogs & derivatives , Substance P/pharmacology , Tumor Cells, Cultured/drug effects , Bombesin/metabolism , Carcinoma, Small Cell , Cell Division/drug effects , Cell Line , Clone Cells , Humans , Lung Neoplasms , Receptors, Bombesin , Receptors, Neurotransmitter/metabolism , Tumor Cells, Cultured/cytology , Tumor Cells, Cultured/metabolism
11.
Exp Cell Res ; 176(2): 336-43, 1988 Jun.
Article in English | MEDLINE | ID: mdl-2837402

ABSTRACT

Small cell lung cancer (SCLC) cell lines were examined for the presence of insulin-like growth factor I-related protein (IGF-I) in cell pellets and culture media. IGF-I immunoreactivity was detected in 11/14 pellets, ranging from 12 to 76 mIU/mg soluble protein. The IGF-I levels in the cell pellets showed a correlation to the corresponding culture media. IGF-I binding sites were found in all tested cell lines. The maximum binding (Bmax) ranged from 131 to 1230 fmol/mg protein and the dissociation constant (KD) from 0.89 to 5.21 nM. The incorporation of [3H]thymidine in the presence of recombinant human IGF-I resulted in a clearly increased DNA synthesis in two of seven cell lines. Thus, IGF-I may be an important growth factor in SCLC.


Subject(s)
Carcinoma, Small Cell/metabolism , Insulin-Like Growth Factor I/biosynthesis , Lung Neoplasms/metabolism , Somatomedins/biosynthesis , Animals , Cell Division/drug effects , Insulin-Like Growth Factor I/pharmacology , Radioimmunoassay , Receptor, Insulin/analysis , Receptors, Somatomedin , Tumor Cells, Cultured
12.
Cancer Res ; 48(5): 1132-6, 1988 Mar 01.
Article in English | MEDLINE | ID: mdl-2830015

ABSTRACT

Non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) cell lines were studied for epidermal growth factor (EGF) receptor expression. All NSCLC cell lines tested (eight of eight) had specific EGF binding sites, whereas only five of 11 SCLC cell lines bound EGF. NSCLC and SCLC cell lines expressed the same type of high affinity EGF binding sites with a Kd of 0.5 to 4.5 nM; however, NSCLC cells bound significantly more EGF than SCLC cell lines. The amount of binding sites in NSCLC cells ranged between 71 and 1,000 fmol/mg of protein and in SCLC cells, between 26 and 143 fmol/mg of protein. The two SCLC cell lines with EGF binding values within the range of NSCLC belonged to the variant subtype of SCLC. By means of an anti-erbB serum and indirect radioimmunoprecipitation, a strong Mr approximately 170,000 protein band could be detected in the NSCLC cell lines. This protein corresponds to the EGF receptor molecule. Its identity was proven by competition with excess erbB antigen for the antibody during the radioimmunoprecipitation. Furthermore, this Mr 170,000 protein exhibited protein kinase activity as evidenced by in vitro autophosphorylation. The radioactivity incorporated into the Mr 170,000 band in radioimmunoprecipitation and protein kinase assays was 10 to 100 times lower in these SCLC cell lines which were positive in the EGF binding assay compared to the NSCLC cell lines. We conclude that NSCLC in contrast to SCLC expresses high levels of EGF receptors which may be used to facilitate the differential diagnosis in some cases of lung cancer. These data suggest that EGF may play a role in growth and differentiation of NSCLC.


Subject(s)
ErbB Receptors/analysis , Lung Neoplasms/analysis , Carcinoma, Small Cell/analysis , Epidermal Growth Factor/metabolism , ErbB Receptors/genetics , Gene Amplification , Humans , Iodine Radioisotopes , Molecular Weight , Protein Kinases/analysis , Temperature , Tumor Cells, Cultured/analysis
13.
J Cancer Res Clin Oncol ; 114(3): 235-44, 1988.
Article in English | MEDLINE | ID: mdl-2838487

ABSTRACT

We investigated the production, binding to cell membranes, and influence on cell proliferation of peptides and growth factors in 4 classic, 5 transitional, and 5 variant SCLC cell lines. Glucagon, neurotensin, and TGF-alpha were present in all cell lines. Bombesin was predominantly found in classic cell lines and insulin in variant cell lines. Neurokinin A, calcitonin, CGRP, GHRF, somatostatin, and CNTF were detectable in some cell lines without prevalence for a particular cell type. We could not detect AVP, growth hormone, neuropeptide Y, substance P, VIP, and NGF. Insulin binding sites were present on 11/14 cell lines, and some cell lines specifically bound bombesin, calcitonin, and EGF. Growth effects were detectable for insulin, GRP-related peptides, tachykinins, and VIP. Using serum-free conditions, insulin and VIP had a growth stimulating effect in liquid culture at nanomolar concentrations. Bombesin and neuromedin B stimulated the clonal growth at a concentration of 3-30 nM. The tachykinins neurokinin A, neurokinin B, physalaemin, and eledoisin inhibited the clonal and mass culture growth with a peak effect in the range of 0.1 to 10 pM. Peptide-induced stimulating and inhibiting effects were within a magnitude of 2-fold. All other peptides and growth factors tested, including ACTH, AVP, calcitonin, glucagon, neurotensin, somatostatin, EGF, CNTF, and NGF did not affect the growth of SCLC. We conclude that the growth of SCLC is partly controlled by such peptides in an autocrine/paracrine fashion.


Subject(s)
Carcinoma, Small Cell/metabolism , Growth Substances/biosynthesis , Lung Neoplasms/metabolism , Peptide Biosynthesis , Amino Acid Sequence , Animals , Binding Sites , Cell Division , Cell Line , Cell Membrane/metabolism , Radioimmunoassay
14.
J Cancer Res Clin Oncol ; 113(6): 579-85, 1987.
Article in English | MEDLINE | ID: mdl-3316242

ABSTRACT

Addition of epidermal growth factor (EGF) to cultures of the urinary bladder carcinoma cell line 5637 regulated proliferation and production of colony stimulating activity (CSA). The optimal concentration range of EGF for stimulation of cell proliferation was 5-20 ng/ml EGF and for production of CSA 2-20 ng/ml EGF. High EGF concentrations (100-200 ng/ml) showed inhibitory effects on proliferation and to a greater extent on CSA production. Also, EGF binding sites of high affinity (kd:3.25 nM) were demonstrated on the cell surface. In the optimal concentration range for stimulation (5-20 ng/ml EGF) EGF binding sites were occupied half-maximally. The loss in EGF binding after long incubation at 37 degrees C was prevented by the lysosomal inhibitory agent, chloroquine. Nonspecific binding of EGF was very low, the amount of maximally bound EGF was 1430 fmol/mg protein (130,000 bound EGF molecules/cell). A strong band of approximately 170,000 daltons could be detected by means of an anti-erbB serum which recognizes the EGF receptor protein. The protein became phosphorylated upon addition of gamma-32P ATP. The data suggest that EGF initiates its action by binding to specific high affinity receptors and plays a role in growth regulation and differentiation of the urinary bladder carcinoma cell line 5637.


Subject(s)
Carcinoma/pathology , Colony-Stimulating Factors/physiology , Epidermal Growth Factor/metabolism , ErbB Receptors/metabolism , Tumor Cells, Cultured/metabolism , Urinary Bladder Neoplasms/pathology , Carcinoma/metabolism , Cell Division , Chemical Precipitation , Humans , Immunologic Techniques , Kinetics , Phosphoproteins/metabolism , Temperature , Tumor Cells, Cultured/cytology , Urinary Bladder Neoplasms/metabolism
15.
Chronobiol Int ; 3(2): 135-9, 1986.
Article in English | MEDLINE | ID: mdl-2824071

ABSTRACT

High affinity serotonin binding to rat brain membranes showed a circadian rhythm with minimal binding at 1000 and a maximal binding at 0000. Brain serotonin levels were almost inverse to the rhythm of serotonin binding. Under reverse light-dark conditions, lights on from 1900 to 0700, a significant phase shift in serotonin binding and concentration of about 8-10 hr was found. The adaptation of the rats to the inverse light-dark cycle was ascertained by plasma ACTH and corticosterone assay.


Subject(s)
Brain/metabolism , Circadian Rhythm , Serotonin/metabolism , Adaptation, Physiological , Adrenocorticotropic Hormone/blood , Animals , Corticosterone/blood , Darkness , Light , Male , Rats , Rats, Inbred Strains
16.
Chronobiol Int ; 3(2): 141-6, 1986.
Article in English | MEDLINE | ID: mdl-2824072

ABSTRACT

Sleep deprivation (SD) modified the circadian rhythm of specific high affinity serotonin (5-HT) binding to rat brain membranes. In control rats a 24-hr rhythm was evident with a trough at 1000-1200 and a nadir at 0000. During the last 26 hr of a 49 hr SD period, trough and peak values were delayed by 4-6 hr. The 24-hr mean binding was significantly (P less than 0.001) different from that of controls. If sleep deprivation was followed by recovery sleep (RS), the normal rhythm of 5-HT binding was obtained already within 1 hr after SD. The effects of SD and RS were ascertained by plasma ACTH and corticosterone assay. No significant change in the hormone rhythms were observed through the mean plasma level of ACTH and corticosterone were enhanced to about 180 and 150%, respectively. Chronic treatment with the antidepressant imipramine resulted in a decrease of the 24-hr mean 5-HT binding by about 50% and a 2-hr delay of peak and trough values. Imipramine treatment decreased the peak value of 5-HT concentration at 1000 to about 65% and appears to abolish the rhythm of 5-HT concentration.


Subject(s)
Circadian Rhythm/drug effects , Imipramine/pharmacology , Serotonin/metabolism , Sleep Deprivation/physiology , Adrenocorticotropic Hormone/blood , Animals , Brain/drug effects , Brain/metabolism , Corticosterone/blood , Male , Rats , Rats, Inbred Strains , Receptors, Serotonin/drug effects , Receptors, Serotonin/metabolism
17.
J Neural Transm Suppl ; 18: 287-94, 1983.
Article in English | MEDLINE | ID: mdl-6192210

ABSTRACT

Crude membrane fractions isolated from rat brain were used to measure specific serotonin (5-HT) binding. In untreated animals a 24 hours rhythm in 5-HT binding was evident. Sleep deprivation (SD) was applied to enhance sleep pressure. After 12, 24, and 72 hours SD the high affinity 5-HT binding, KD1 = 1-3 nM, remained unchanged, the apparent dissociation constant of the low affinity 5-HT binding, KD2 = 20-30 nM, was found to be enhanced almost by factor 2. The number of binding sites were only moderately affected by SD. If SD was followed by 1 or 4 hours recovery sleep, the dissociation constant KD2 was decreased towards control values. The brain levels of 5-HT and 5-hydroxyindoleacetic acid (5-HIAA) were not significantly changed immediately after 72 hours SD. A statistically significant increase was found only for 5-HIAA 4 hours after 72 hours SD. The results are consistent with the hypothesis that changes in the sensitivity of 5-HT binding may be involved in the regulation of the sleep-waking cycle.


Subject(s)
Brain/metabolism , Circadian Rhythm , Serotonin/metabolism , Sleep Deprivation , Animals , Hydroxyindoleacetic Acid/metabolism , Kinetics , Rats , Time Factors
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