Frog olfaction: odour groups, acceptor distribution and receptor categories

A numerical matrix of electrophysiological data on odour discriminationin frog's olfactory receptors has been published by Revial etal. (1978). Pearson's "r" correlation coefficient and Benzecri's"analyse des correspondences" were used to analyse the informationcontained in the original matrix about similarities betweenodours and between receptors. Data analysis revealed five factorsthat accounted for 71% of the total variance, with one factormarkedly prevailing over the other four. Camphoraceous compoundswere opposed to aromatic compounds with respect to this firstfactor. Four groups of odorants were evidenced: i—an aromaticgroup including benzene, anisole, bromobenzene and dichlorobenzene;thiophenol seems to be related to this group; ii—a camphoraceousgroup with camphor and cineole; iii—a group includingcyclohexanol, cyclohexanone and tert-butyl alcohol; iv—afatty acid group with butyric, valeric and isovaleric acids.In addition, a sulphur group represented by thiophene is suggested.The functional implications of the groups are discussed. Itis proposed that a group is due to a number of types of acceptorsites sharing some common, sterical and energetical properties.Receptor cells combine multiple sensitivities and, consequently,do not fall under simple categories.     

Social organisation and interspecific interactions in two sympatric species of Ranidella (Anura)

Summary The socio-spatial organisation of two sympatric species of anurans was investigated by analyses of the spatial and temporal structure of breeding assemblages. Ranidella signifera breeds earlier in the year than its congener, R. parinsignifera, though there is an overlap of 6 to 8 weeks. Males of both species show high affinities for discrete spatial locations (preferred calling stations). These stations are regularly-spaced, and temporally-stable. Satellite behaviour occurs, though most satellites are past or future residential males. There appears to be a spatial-energetic limit to the number of calling residents of both species that a pond can support. There is no differentiation of calling sites between the two species, and the males of R. parinsignifera appear to displace their congeners from the preferred stations located on the land/water interface of ponds. The breeding season of R. signifera in sympatry is abbreviated relative to nearby (20 km) allopatric localities. The breeding seasons of conspecific males and females are well-synchronised, though the ratio of males to females is high early in the breeding season.     

Stimulation of the adenylate cyclase of A B16 melanoma cell line by pro-opiocortin-related peptides--a structure-activity study

The ability of alpha-melanotrophin (alpha-MSH or ACTH 1-acetyl-13 amide) and other structurally related peptides derived from the common precursor, pro-opiocortin, to stimulate adenylate cyclase activity in a pigmented B16 mouse melanoma was investigated. The peptides ACTH 1-39, ACTH 1-24, alpha-MSH, ACTH 1-13 amide and beta-MSH all stimulated the enzyme to a similar maximal extent and with similar potency (ED50 = 1.3 . 10(-6) M) except that ACTH 1-39 was slightly less potent (ED50 = 5 . 10(-6) M). ACTH 4-10 (ED50 = 4 . 10(-5) M) and gamma-MSH (ED50 = 5 . 10(-6) M) were partial agonists. ACTH 1-10 was no more effective than ACTH 4-10 in stimulating the enzyme whereas ACTH 1-13 amide was a full agonist. The peptides beta-endorphin and its derivatives, Met-enkephalin and melanotrophin potentiating factor (MPF), failed to stimulate the enzyme. We suggest that the B16 melanoma requires not only the sequence ACTH 4-10 but also some part of the sequence ACTH 11-13, or a similar sequence in the terminal portion of beta-MSH, for full activation of the receptor-linked enzyme.     

Chromatographic resolution of amino acid adducts of aliphatic halides

Numerous xenobiotics are known to be bioactivated and to covalently bind to proteins, but the resulting amino acid adducts (AAAs) are unknown. In this study the AAAs of twelve ¹⁴C-labeled aliphatic halides were examined after formation in an in vitro microsomal system. After exhaustive solvent extraction of the precipitated microsomal protein, the AAAs were isolated by Pronase digestion, followed by filtration through a 500 mol. wt. exclusion membrane. The liberated AAAs were applied to a constant flow DC-4A cation exchange column, resolved by stepwise buffer elution, collected and counted for radioactivity. Column recovery for applied radioactivity was 100 ± 4%. Generally, 1–4 different AAAs (defined by eluting radioactivity) were resolved, with each organohalogen displaying a characteristic elution profile. Methyl iodide, trichloroethylene and 1,2-dichloroethylene had a single major AAA while bromotrichloromethane, 1,2-dibromoethane, 1,1,1-trichloroethane, 1,2-dichloroethane, 1,1,2-trichloroethane, 2-bromo-2-chloro-1,1,1-trifluoroethane, chloroform and carbon tetrachloride had up to 4 AAAs or more, indicating combinations of binding site(s) and reactive intermediate(s). The single AAA formed following incubation of methyl iodide with the microsomes was identified as S-methylcysteine. Thus, this method appears capable of resolving binding sites and is the initial isolation step for identifying specific adducts to proteins.     

In vitro studies on the growth of Shigella sonnei by Lactobacillus casei and Lact. acidophilus.

The inhibitory effect of lactobacilli on growth of Shigella sonnei was studied. The effect was not due to pH alone, as addition of hydrochloric, lactic or acetic acids to culture media did not inhibit the normal growth of the shigellas. The degree of inhibition was measured by disc assay and showed that the inhibitory substance(s) can be extracellular and diffusible, varying the degrees of inhibition depending on the media tested. When broth was inoculated with mixed cultures of Lactobacillus and Shigella strains, the inhibition began at 6 h and the death phase at 9 h. The higher inhibition was produced by the mixture of lactobacilli (35.5 +/- 2.5% at 6 h culture, 57.4 +/- 1.9% at 9 h and 91.2 +/- 1.2% at 14 h). The degree of inhibition was higher when the relationship pathogen : lactobacilli was 1:10(3). The specific growth rate of lactobacilli and shigella was different in pure or mixed cultures. When the lactobacillus alone was grown for 12 h and the shigellas then added, the numbers of shigellas began to decrease immediately at 37 degrees C. This work shows that the Lactobacillus strains employed in fermented milk can be used to inhibit the growth of Sh. sonnei.     

Adenylate cyclase of human articular chondrocytes. Responsiveness to prostaglandins and other hormones.

Adenylate cyclase [ATP pyrophosphate lyase (cyclizing), EC 4.6.1.1] was shown to be present in cultured human articular chondrocytes. Optimal conditions of incubation time, protein and substrate concentrations and pH were determined in whole cell lysates. Maximal activity occurred at pH 8.5 with no decrease in activity up to pH 10.0. Adenylate cyclase activity of particulate membrane preparations was enhanced by the addition of crude cytosol preparations. The prostaglandins E1, E2, F1 alpha, F2 alpha, D2, B1, B2, A1 and A2, as well as adrenaline and isoprenaline, stimulated adenylate cyclase derived from either adult or foetal chondrocytes. No significant stimulation was observed in the presence of human calcitonin or glucagon. Bovine parathyroid hormone always significantly stimulated the adenylate cyclase derived from foetal chondrocytes, but not from adult chondrocytes. Preincubation of the chondrocytes in culture with indomethacin and with or without supernatant medium from cultured mononuclear cells increased the responsiveness of the adenylate cyclase to prostaglandin E1.     

Cooperative interaction of reduced pyridine nucleotides with estrogen synthetase of human placental microsomes

The estrogen synthetase present in human placental microsomes appears to be dependent on the cooperative interaction of the reduced cofactors NADPH and NADH for optimal activity. Using steady-state concentrations of either cofactor, it was found that while the estrogen synthetase activity followed hyperbolic saturation kinetics with NADPH (K_mapp = 14 μM), the enzyme followed sigmoidal saturation kinetics when the cofactor was NADH, with the half-maximum velocity attained at a cofactor concentration of 1.1 mm. The maximum velocity obtained with NADPH as the cofactor was greater than with corresponding concentrations of NADH. Estrogen synthetase activity in the presence of NADH was not due to NADPH contamination. NADH, in the presence of small concentrations of NADPH (0.5 to 5 μm), stimulated significantly the rate of estrogen formation from androstenedione by placental microsomes and, in addition, the enzyme saturation kinetics changed from sigmoidal to hyperbolic, thus mimicking the effect of NADPH. Estrogen synthetase activity, measured in the presence of 1 mm NADH, was stimulated in a dose-dependent manner by NADPH (K_mapp = 0.4 μM NADPH) and, when the enzyme was measured in the presence of 5 μm NADPH, the activity was stimulated in a dose-dependent manner by NADH (K_mapp = 45 μM NADH). Estrogen synthetase activity measured in the presence of NADH, without and with NADPH (1 μm) remained linear both with time of incubation for approximately 15 min and with microsomal protein concentration up to 3 mg/ml. The apparent K_m of estrogen synthetase for androstenedione, when measured in the presence of NADH, was 1 μm. The synergistic interaction between NADH and NADPH in stimulating placental estrogen synthetase activity observed in vitro may, conceivably, take place in vivo in the intact placenta.     

Evidence that calmodulin may be involved in phytohaemagglutinin-stimulated lymphocyte division

Phytohaemagglutinin-stimulated and non-stimulated incorporation of [³H]thymidine into human peripheral blood lymphocytes is inhibited by the calcium antagonist PY 108–068 and by the calmodulin antagonists trifluo-perazine andN-(6-aminohexyl)-5-chloro-l-naphthalene sulphonamide (W7). It is argued that calmodulin may be involved in both non-stimulated [³H]thymidine uptake in lymphocytes and also in the lymphocyte response to phytohaemagglutinin.     

Population biology of parasites of striped mullet, Mugil cephalus L. I. Monogenea

Young-of-the-year (class 0) and yearling (class 1) striped mullet, Mugil cephalus , were collected from Sapelo Island, Georgia from May 1970 to June 1971 to study the development, seasonal abundance and relationship of environmental variables to parasitic populations. The number of species of parasites increased with age of the host. Initial infection appeared to be influenced by closeness of association of mullet age classes, by the period of abundance of a parasite on class I mullet and by the mobility of the infective parasitic stage. Fluctuations in intensity and prevalence of a parasite on class 0 mullet were similar to those of class I mullet after the initial infection. Ancyrocephalus vanbenedenii was first observed on class 0 mullet in March. Intensity was high on both classes in spring and on reproductively active mullet in late autumn. Prevalence on both classes was above 80% except in late summer. Polyclithrum mugilis was not observed on class 0 mullet until August even though intensity and prevalence on class I mullet was highest during early spring. Gyrodactylus mugelus did not occur on class 0 mullet but appeared on class I mullet during late summer. Microcotyle psuedomugilis was observed on class 0 mullet in early summer and Metamicrocolyla maeracantha in October. Both species occurred but at a low intensity on class I mullet.