Captopril (SQ 14,225): In vitro and in vivo influence on the proliferative response of rat lymphocytes

Summary Captopril in vitro (50–500 g/ml) increased³H-TdR incorporation in unstimulated and mitogen-stimulated cultures of rat lymphocytes. Unseparated spleen and lymph node cells of rats orally treated with captopril (50 mg/kg/day×4) showed decreased basal and mitogen stimulated³H-TdR incorporation. The removal of macrophages abrogated this inhibitory effect. Leucine aminopeptidase activity of macrophages was reduced — in vivo and in vitro — by captopril.Acknowledgments. The authors thank the Squibb Institute for Medical Research for the gift of Captopril. The excellent technical assistance of Ms B. Hasselriis, Ms B. Rumler and Ms E. Greve Petersen is gratefully acknowledged.     

Peritoneal macrophages from adjuvant arthritic rats enhance tumour cell growth in vitro.

Peritoneal macrophages from rats with adjuvant arthritis enhance the incorporation of 3H-thymidine in 2 tumour cell lines in vitro. Maximal enhancement is found during the development of the secondary lesions, and it is suggested that the immunologic commitment of the macrophages could interfere with their regulation of tumour cell proliferation in vivo.     

Effects of cadmium on the immune system of mice

Summary Chronic oral exposure of mice to Cd⁺⁺ inhibits cell-mediated immunity of delayed type hypersensitivity induced by sheep red blood cells (SRBC). No effect was detected on humoral immune response to SRBC. Spleen cells derived from mice exposed to Cd⁺⁺ showed in vitro enhanced response to T and B cell mitogens. These results demonstrate that Cd⁺⁺ exposure alters the immune system of mice.Dedicated to Prof. Georg Henneberg on the occasion of his 70th anniversary on 12.10.1978.Acknowledgments. Supported by a grant from the Umweltbundesamt. We thank Ms Odenwald, Ms Schulz, Klinikum Steglitz, and Ms Emeis, Robert Koch-Institut Abt. Immunologie, for the excellent technical assistance.     

Plakorin,a potent Ca2+-ATPase activator from the Okinawan marine spongePlakortis sp.

Summary A new cyclic peroxide, plakorin, which is a potent sarcoplasmic reticulum (SR) Ca^a+-ATPase activator has been isolated from the Okinawan marine spongePlakortis sp., its structure was elucidated on the basis of spectral data.Acknowledgments. We thank Ms M. Hamashima and Ms A. Muroyama for their technical assistance.     

Light dependent accumulation of macrophages at the photoreceptor-pigment epithelial interface in the retina of albino mice

Summary In the subretinal space of albino mice, macrophages appear from the time of eye opening and increase in number for 6 months; thereafter they decline with age. Dark rearing retards the accumulation of these cells, and exposure to constant light results in a rapid increase. Observations suggest that macrophages appear as a response to visual cell decay in albino mice and supplement the phagocytic activity of the pigment epithelium.We thank R.K. Hawkins for efficient management of the animal colony, H.G. Jansen for cooperation in the use of electron microscope and Ms Paula van Alphen for help in preparation of the illustrations.     

Symbioramide,a novel Ca2+-ATPase activator from the cultured dinoflagellateSymbiodinium sp.

Summary A novel sphingosine derivative, symbioramide, has been isolated from the laboratory-cultured dinoflagellateSymbiodinium sp. as a sarcoplasmic reticulum (SR) Ca²⁺-ATPase activator, and its structure elucidated to be1 on the basis of spectral and chemical means.Acknowledgments. We thank Ms M. Hamashima and Ms A. Muroyama for their technical assistance.     

Effect of salt concentration on binding of proteins to a non-ionic adsorbent

Summary The effect of NaCl concentration on the adsorption of several proteins to palmityl-substituted Sepharose 4B has been investigated. It has been observed that the degree of adsorption first decreases and then increases with increasing salt concentrations, followed by total immobilization. The results are qualitatively explained by the simple theory of Debye-Hückel-Kirkwood, as applied to poly-electrolytes in the presence of salt.Acknowledgments. The authors wish to thank Ms H. Keshavarzi, Ms J. Nobakht and Mr F. Mohanazadeh for their technical assistance.     

Synthesis,crystallization and properties of acetyl phenylalanyl lysine chloromethyl ketone: A potential inhibitor of serine proteases

Summary A procedure for the synthesis of acetyl phenylalanyl lysine chloromethyl ketone is described. The chloromethyl ketone derivative is a noncompetitive inhibitor of trypsin (K₁=5.9×10^–3 M).Acknowledgments. The authors are grateful to Dr Arthur L. Bacon for his constant support and encouragement. Special thanks are due to Dr William Kray for initiating this research project. We thank Mrs Juliette Barclay, Ms Earlene Spratling and Ms Ollivette Hill for their technical assistance in conducting some of the experiments. This investigation was supported by MBS grant RR8105 from the General Research Support Branch, Division of Research Resources, National Institutes of Health.     

α-Adrenoceptor blocking action of hymenin,a novel marine alkaloid

Summary In the rabbit isolated aorta, hymenin (10^–6 M) a novel marine alkaloid, caused a parallel rightward shift of the dose-response curve for norepinephrine without affecting that for histamine or KCl, suggesting that hymenin is a competitive antagonist of -adrenoceptors in vascular smooth muscles.Acknowledgments. We thank Ms A. Kajiwara and Ms M. Hamashima of this institute for their technical assistance, and Prof. Y. Hirata of Meijo University for his encouragement.     

Methyllycaconitine,a naturally occurring insecticide with a high affinity for the insect cholinergic receptor

Summary Studies of extracts ofDelphinium seeds, long known to be insecticidal, revealed that a principal insecticidal toxin was methyllycaconitine, which is shown to be a potent inhibitor of -bungarotoxin binding to housefly heads (K_inh=2.5×10^–10±0.5×10^–10M).Calgary for gifts of MLA, citrate and lycoctonine, and Dr W. Bowers of the University of Arizona for the original extract ofDelphinium seeds. We would also like to acknowledge the able technical support of Ms C. Dushin, Mr E.L. Bowman, Dr C. C. Gagne, Mr R. F. Borysewicz and Dr P. Mowery for his assistance in obtaining and interpreting the carbon-13 NMR spectra.     

Lymphatic metastasis of tumour; persistent transport of cells

Summary A model of lymphatic metastasis established by injecting Walker rat carcinoma cells into the rat footpad was used to study the output of tumour cells from the footpad. The lymphatic efferent from the footpad was cannulated in a group of rats with advanced neoplasm; it was shown that the output of tumou cells was continuou over periods up to 90 min and ranged from 10²–10⁵ cells/min.Acknowledgment. This work was supported by a grant from the National Cancer Institute of Canada to C.R.F. and I.C. We are grateful to Mrs W. Kao and Mr I. Etches for meticulous technical help and to the Photographic Section, Department of Pathology for illustrations. Dr V.S. Gupta of Veterinary Physiology, University of Saskatchewan supplied the tumour for transplantation.     

Human albumin synthesis via an albumin precursor in liver tissue slices

Summary A precursor of plasma albumin in man was identified in liver obtained from cadaver renal transplant donors. After 30 min incubation with¹⁴C-(U) leucine, most of the labeled immunoreactive albumin was identified as proalbumin, as was evident from its characteristic elution profile on DEAE cellulose 52. After an additional 30 min incubation with unlabeled leucine (60 min total), no precursor from could be identified and the label coeluted with serum albumin. These data strongly suggest that human albumin is initially synthesized in a precursor form and is subsequently transformed into serum albumin.This work was supported by grants from the Deutsche Forschungsgemeinschaft, the National Institutes of Health (CA 123896, AM 191241, CA 142940), and the Hochschulstiftung an der Universität Bern.We gratefully acknowledge the excellent technical assistance of Ms Kathleen O'Laughlin and Ms Edith Junker-Riesen.     

Semi-synthesis and proposed structure of platelet-activating factor (P.A.F.): PAF-acether an alkyl ether analog of lysophosphatidylcholine]

We have studied the molecular structure of platelet-activating factor" (P.A.F.), a mediator of inflammation obtained from blood leukocytes, macrophages, and platelets themselves. We have semi-synthetized a substance that possesses all the known physicochemical and biological characteristics of P.A.F. from hog leukocytes. This was performed by successive methylation, hydrogenation, and acetylation of lysophosphatidylethanolamine plasmalogen. We therefore propose the following structure for P.A.F.: 1-0-alkyl-2-acetyl-glyceryl-3-phosphorylcholine. This molecular structure is not yet described among the numerous substances capable of inducing platelet aggregation and release.     

Suppressed collagenolytic activity in polymorphonuclear leucocytes from diabetic humans

Summary Extracts of polymorphonuclear leucocytes (PMNL) from diabetic human exhibited less collagenolytic activity than extracts from normoglycemic control subjects. Partially purified control extracts produced ^A and ^B collagen breakdown products of the type generated by mammalian collagenase; the diabetic preparation produced decreased amounts of the same products. The diabetic PMNLs may synthesize abnormally low levels of collagenase or contain inactive forms of this enzyme.Supported by a grant (No. DE-03987) from the National Institute of Dental Research (N.I.H.), USA. This study forms part of the Ph.D. thesis of G.A. Nicoll.Acknowledgments. The authors wish to thank Ms Salema Karim and Mr F.R. Singh for excellent technical assistance.     

Effects of propafenone on TEA-induced action potentials in vascular smooth muscle of canine coronary arteries

Summary The Ca⁺⁺-dependent, TEA-induced action potential is blocked by propafenone in a dose-dependent manner. Such results suggests that in coronary arterial smooth muscle one mechanism of action of propafenone is to inhibit Ca⁺⁺ inward current.This research was supported by a grant from the Tennessee Affiliate of the American Heart Association and VA grant No. 1A (74)111-430100). The authors wish to thank Dr Gerhard Pfennigsdorf for supplying us with propafenone. We also wish to thank Ms Penny Williams for her technical assistance.     

Bactericidal activity againstPseudomonas aeruginosa is acquired by cultured human monocyte-derived macrophages after uptake of myeloperoxidase

Myeloperoxidase (MPO) is an enzyme located within polymorphonuclear neutrophils capable of producting cytotoxic oxidant species that are particularly active against bacteria with polysaccharide capsules.Pseudomonas aeruginosa (10⁶ bacteria per 1 ml) are killed within 1 h in vitro by a MPO/H₂O₂/Cl^– system (48 mU=132 ng of MPO). The question arose as to whether human macrophages would acquire cytotoxic activity when loaded with this enzyme. Monocytes were therefore isolated from human blood and cultured for up to ten days to induce maturation to macrophages. These cells lost endogenous MPO within five days while H₂O₂ production in response to stimulation by phorbol myristate acetate (10^–6M) decreased to 23% within ten days. On the other hand, their capacity to take up exogenous MPO increased fourfold from day three to day ten. Human macrophages cultured from eight days (when both H₂O₂ production and MPO uptake were sufficient) were therefore used to study the effects of MPO uptake on cytocidal activity againstPseudomonas aeruginosa. After a 1 h MPO loading period, macrophages (5×10⁵ cells per ml) were incubated in the presence of bacteria (0.5 to 2×10⁶ bacteria per ml) for 2 h at 37°C. At a bacteria/macrophage ratio of 1, only 34.8±7.0% of bacteria survived (compared to killing by non-loaded macrophages), while 74.4±9.3% survived at a ratio of 4. From these results, we conclude that loading macrophages with exogenous MPO could enhance their microbicidal activity, suggesting a potentially useful therapeutic application.     

9-Methyl-7-bromoeudistomin D,a potent inducer of calcium release from sarcoplasmic reticulum of skeletal muscle

Summary The Ca²⁺-releasing action of several derivatives of eudistomin D isolated from a marine tunicate was compared with that of caffeine. It was found that 9-methyl-7-bromoeudistomin D was approximately 1000 times more potent than caffeine in causing Ca²⁺ release from the sarcoplasmic reticulum.The authors thank Ms A. Muroyama of this institute for her technical assistance and Prof. K. L. Rinehart of University of Illinois for his encouragement.     

Effects of the optical isomers of 2-amino-3-fluoro-1-phenylpropane (monofluoroamphetamine) hydrochloride on uptake and release of dopamine in rat striatum in vitro

Summary The (+)- and (–)-isomers of the monofluorinated amphetamine 2-amino-3-fluoro-1-phenylpropane were prepared and compared for their ability to stimulate release and to inhibit reuptake of radiolabelled dopamine from rat striatal tissue in vitro. The (+)-isomer was much stronger than the (–)-isomer in both cases.Financial support for this project was supplied by the Medical Research Council of Canada, the Alberta Mental Health Research Fund and the Special Services and Research Committee, University of Alberta Hospital.Acknowledgments. Skilled technical assistance was provided by Ms L. Hiob. The authors also wish to thank Dr W.G. Dewhurst, Department of Psychiatry, and Dr D.F. LeGatt, for their advice and comments.     

Targeting O 6-methylguanine-DNA methyltransferase with specific inhibitors as a strategy in cancer therapy

O ⁶-methylguanine-DNA methyltransferase (MGMT) repairs the cancer chemotherapy-relevant DNA adducts, O ⁶-methylguanine and O ⁶-chloroethylguanine, induced by methylating and chloroethylating anticancer drugs, respectively. These adducts are cytotoxic, and given the overwhelming evidence that MGMT is a key factor in resistance, strategies for inactivating MGMT have been pursued. A number of drugs have been shown to inactivate MGMT in cells, human tumour models and cancer patients, and O ⁶-benzylguanine and O ⁶-[4-bromothenyl]guanine have been used in clinical trials. While these agents show no side effects per se, they also inactivate MGMT in normal tissues and hence exacerbate the toxic side effects of the alkylating drugs, requiring dose reduction. This might explain why, in any of the reported trials, the outcome has not been improved by their inclusion. It is, however, anticipated that, with the availability of tumour targeting strategies and hematopoetic stem cell protection, MGMT inactivators hold promise for enhancing the effectiveness of alkylating agent chemotherapy.     

The effect of Valium® anaesthesia on the radiosensitivity of the skin of the mouse foot

Summary Valium^® anaesthesia significantly reduces the effect of large single doses of X-rays on the mouse foot skin as compared with Nembutal^® anaesthesia. The radioprotective action of Valium may be attributed to a direct effect on the cells of the skin.Supported by the Swiss National Science Foundation (Grant no. 3.682-0.75).Acknowledgments. The authors wish to thank Miss F.T. Josuran, Miss U. Schärer and Mr P.P. Binz for their excellent technical assistance with the experiments.