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The methanol solvomorph 1 amp; 8201; amp; 8901; amp; 8201;2MeOH of the cobalt II complex [Co LSal,2 amp; 8722;Ph 2] 1 with the sterically demanding Schiff base ligand 2 [1,1 amp; 8242; biphenyl] 2 ylimino methyl phenol HLSal,2 amp; 8722;Ph shows the thus far largest dihedral twist distortion between the two chelate planes compared to an ideal pseudotetrahedral arrangement. The cobalt II ion in 1 amp; 8201; amp; 8901; amp; 8201;2MeOH exhibits an easy axis anisotropy leading to a spin reversal barrier of 55.3 amp; 8197;cm amp; 8722;1, which corresponds to an increase of about 17 amp; 8201; induced by the larger dihedral twist compared to the solvent free complex 1. The magnetic relaxation for 1 amp; 8201; amp; 8901; amp; 8201;2MeOH is significantly slower compared to 1. An in depth frequency domain Fourier transform FD FT THz EPR study not only allowed the direct measurement of the magnetic transition between the two lowest Kramers doublets for the cobalt II complexes, but also revealed the presence of spin phonon coupling. Interestingly, a similar dihedral twist correlation is also observed for a second pair of cobalt II based solvomorphs, which could be benchmarked by FD FT THz EPR

A cobalt(II)‐based spin triangle shows a significant spin–electric coupling. [Co3(pytag)(py)6Cl3]ClO4⋅3 py crystallizes in the acentric monoclinic space group P21. The intra‐triangle antiferromagnetic interaction, of the order of ca. −15 cm−1 (H=−JSaSb), leads to spin frustration. The two expected energy‐degenerate ground doublets are, however, separated by a few wavenumbers, as a consequence of magnetic anisotropy and deviations from threefold symmetry. The Co3 planes of symmetry‐related molecules are almost parallel, allowing for the determination of the spin–electric properties of single crystals by EFM‐ESR spectroscopy. The spin–electric effect detected when the electric field is applied in the Co3 plane was revealed by a shift in the resonance field. It was quantified as ΔgE/E=0.11×10−9 m V−1, which in terms of frequency corresponds to approximately 0.3 Hz m V−1. This value is comparable to what was determined for a Cu3 triangle despite the antiferromagnetic interaction being 20 times larger for the latter., This contribution describes the observation of spin–electric coupling utilizing electric‐field‐modulated ESR (EFM‐ESR) spectroscopy for single‐crystals of a spin triangle which is characterized by the strong magnetic anisotropy of the individual cobalt(II) centers and a pronounced sensitivity of the molecular energy levels on the relative orientation of their magnetic axes as well as the exchange coupling between them.

A large single crystal of a compound from the family of coordination polymer [Co(NCS)2(L)2]n chains was synthesized and its magnetic properties are reported. [Co(NCS)2(4-(3-phenylpropyl)pyridine)2]n is ferromagnetic with Tc = 3.39 K. Single-ion ab initio calculations predict an almost Ising-type magnetic anisotropy and the direction of the magnetic easy-axis nearly along the Co–Npy bond of the apical pyridine-based co-ligand. Both predictions are confirmed by single-crystal magnetic measurements. The magnetic relaxation of the single crystal sample significantly differs from the powder sample data, and clearly shows the presence of two separate relaxation processes. The process dominant below 3.2 K demonstrates a single chain magnet (SCM) behaviour, with a crossover between single-wall and two-wall processes, in spite of the fact that the system is ferromagnetically ordered. The faster process that dominates just below Tc is attributed to spin waves. Micromagnetic Monte Carlo simulations of the investigated compound show that the dipolar field cancels for some chains located at the border between 3-dimensional domains. Such chains are responsible for the measured ac signal, and demonstrate the SCM behaviour. The quantitative analysis of the SCM relaxation time is supported by preparing and examining a corresponding diamagnetically diluted compound, [CoxCd1−x(NCS)2(4-(3-phenylpropyl)pyridine)2]n (x = 0.013), which behaves as a field-induced single-ion magnet. The relaxation pathways for single Co(II) spins are determined to be Raman, direct, and quantum tunneling processes, which were included in an improved approach to describe the magnetic relaxation in the Co(II)-based SCM compound.

No previous study assessed the combined effect of olive pruning residues (OLPR) and spent coffee grounds (SCG) on P. ostreatus production and nutritional value. The aim of this study was to determine the capacity of P. ostreatus to degrade lignocellulosic nature of combined OLPR and SCG as well as their resultant nutrient composition. A complete randomized design was adopted with five treatments: S1:100%wheat straw (WS) (control), S2:33%WS+33%SCG+33%OLPR,S3:66%WS+17%SCG+17%OLPR,S4:17%WS+66%SCG+17%OLPR, and S5:17%WS+17%SCG+66%OLPR, and ten replicates per treatment. Substrate’s and mushroom’s composition were analyzed on chemical scale, including fatty acids and heavy metals profiles, following international standards. Only S1, S2, and S3 were productive, with comparable biological yield, economical yield, and biological efficiency. Organic matter loss decreased with increasing proportions of OLPR and SCG. Percentage lignin loss was higher in S1 than in S2 and S3 (53.51, 26.25, and 46.15% respectively). Mushrooms of S3 had some enhanced nutritional attributes compared to control: decrease in fat, increase in protein, increase in monounsaturated fatty acids, and lower zinc accumulation. Lead was less accumulated in S2 than S1 mushrooms. Sodium content of mushroom decreased in S2 and S3. The latter substrates yielded mushrooms with lower polyunsaturated fatty acids (PUFA) and higher saturated fatty acids (SFA) contents. All mushrooms had a valuable PUFA/SFA. This study suggests using OLPR and SCG in low proportions as nutritional supplements to the commercial wheat straw.

Magnetic properties of coordination polymers like single-chain magnets (SCMs) are based on magnetic domains, which are formed due to magnetic exchange between neighboring anisotropic spin centers. However, the computational restrictions imposed by the high level of theory needed for an adequate ab initio quantum mechanical treatment on the basis of multi-reference methods for these systems limit the feasibility of such calculations to mononuclear fragments as appropriate structural cutouts for the metal centers along the chains. Hence, results from such calculations describe single-ion properties and cannot be directly correlated with experimental data representing magnetic domains. We present a theoretical approach based on n-membered Ising-spin rings with n = 3-12, which allows us to simulate magnetic domains and to derive important magnetic properties for SCM compounds. Magnetic exchange, which is not provided by calculations of mononuclear fragments, is obtained by fitting the theoretical magnetic susceptibility against experimental data. The presented approach is tested for cobalt(ii)-based SCMs with three types of repeating sequences, which differ in nuclearity and symmetry. The magnetic parameters derived using the presented approach were found to be in good agreement with the experimental data. Moreover, the energy spectra obtained for the three test cases using the presented approach are characteristic of a deviation of the individual systems from the ideal Ising behavior. An extrapolation technique towards larger systems (n > 12) is presented which can provide information on the statistical mean length of the magnetic domains in the three investigated SCM compounds.

Reaction of Co(NCS)2 with different coligands leads to the formation of three compounds with the general composition [Co(NCS)2(L)2]n (L = aniline (1), morpholine (2), and ethylenethiourea (3)). In ...

Reaction of Co(NCS)2 with 4-bromopyridine leads to the formation of discrete complexes with the composition Co(NCS)2(4-bromopyridine)4·(CH3CN)0.67 (1), Co(NCS)2(4-bromopyridine)2(H2O)2 (2), Co(NCS)2(4-bromopyridine)2(CH3OH)2 (3) and Co(NCS)2(4-bromopyridine)2(CH3CN)2 (4). Upon heating compounds 2 and 4 transform into a crystalline product with the composition Co(NCS)2(4-bromopyridine)2 (5-I) that also can easily be obtained from solution. In this compound, the Co cations are linked by single μ-1,3-bridging thiocyanate anions into layers. Thermal decomposition of 3 leads to a second isomer (5-II), which is thermodynamically metastable and can also be synthesized from solution under kinetic control. In contrast to 5-I, the Co cations are linked by pairs of anionic ligands into linear chains. The magnetic exchange is very weak in 5-I, but much stronger and ferromagnetic along the linear chains in 5-II. AF ordering in 5-II is reached at 3.05 K, and magnetic relaxation is observed at the metamagnetic transition with an Arrhenius barrier of 17.1(3) cm-1. Ab initio computational studies reveal a different type of magnetic anisotropy to be present in the two crystallographically - independent Co centers in 5-II.

The cobalt(II) in [Co(NCS)2(4‐methoxypyridine)2]n are linked by pairs of thiocyanate anions into linear chains. In contrast to a previous structure determination, two crystallographically independent cobalt(II) centers have been found to be present. In the antiferromagnetic state, below the critical temperature (T c=3.94 K) and critical field (H c=290 Oe), slow relaxations of the ferromagnetic chains are observed. They originate mainly from defects in the magnetic structure, which has been elucidated by micromagnetic Monte Carlo simulations and ac measurements using pristine and defect samples. The energy barriers of the relaxations are Δτ1=44.9(5) K and Δτ2=26.0(7) K for long and short spin chains, respectively. The spin excitation energy, measured by using frequency‐domain EPR spectroscopy, is 19.1 cm−1 and shifts 0.1 cm−1 due to the magnetic ordering. Ab initio calculations revealed easy‐axis anisotropy for both CoII centers, and also an exchange anisotropy Jxx/Jzz of 0.21. The XXZ anisotropic Heisenberg model (solved by using the density renormalization matrix group technique) was used to reconcile the specific heat, susceptibility, and EPR data., Slowly relax… The magnetic properties of the linear chain compound [Co(NCS)2(4‐methoxypyridine)2]n have been investigated both experimentally and theoretically. Slow relaxations of the ferromagnetic chains were observed in the antiferromagnetic state and the specific heat, susceptibility, and EPR data obtained have been reconciled by using the XXZ anisotropic Heisenberg model (see figure).

Two different isomers of [Co(NCS)2(4-chloropyridine)2]n (3C and 3L) were synthesized from solution and by thermal decomposition of Co(NCS)2(4-chloropyridine)2(H2O)2 (2), which show a different meta...

Two new transition metal thiocyanate coordination polymers with the composition [Co(NCS)2(4-vinylpyridine)2]n (1) and [Co(NCS)2(4-benzoylpyridine)2]n (2) were synthesized and their crystal structures were determined. In both compounds the Co cations are octahedrally coordinated by two trans-coordinating 4-vinyl- or 4-benzoylpyridine co-ligands and four μ-1,3-bridging thiocyanato anions and linked into chains by the anionic ligands. While in 1 the N and the S atoms of the thiocyanate anions are also in trans-configuration, in 2 they are in cis-configuration. A detailed magnetic study showed that the intra-chain ferromagnetic coupling is slightly stronger for 2 than for 1, and that the chains in both compounds are weekly antiferromagnetically coupled. Both compounds show a long range magnetic ordering transition at Tc = 3.9 K for 1 and Tc = 3.7 K for 2, which is confirmed by specific heat measurements. They also show a metamagnetic transition at a critical field of 450 Oe (1) and 350 Oe (2), respectively. Below Tc1 and 2 exhibit magnetic relaxations resembling relaxations of single chains. The exchange constants obtained from magnetic and specific heat data are in good accordance with those obtained from constrained DFT calculations carried out on isolated model systems. The ab initio calculations allowed us to find the principal directions of anisotropy.

[Co(NCS)2(py)2]n (py = pyridine) is composed of ferromagnetic chains of Co(ii) cations connected by double NCS bridges. The chains are irregular because of two crystallographically inequivalent Co(ii) cations. The coordination polyhedron of the Co(ii) cations is a distorted octahedron built from two N and two S atoms of four equatorial NCS anions and two apical N atoms of the pyridine ligands. Magnetic and specific heat studies show that the compound undergoes a phase transition at 3.7 K to a ferromagnetic state. The determined magnetic interactions, intrachain (J/kB = 28 K) and interchain (zJ'/kB = 0.5 K), confirm the quasi 1D Ising magnetic character of [Co(NCS)2(py)2]n. Using AC magnetic susceptibility measurements the energy barriers for magnetization reversal of different relaxation processes were determined including those of the individual chains. By means of high field-high frequency ESR study the magnetic excitations were observed and explained in the frame of the Ising model in agreement with the results of the magnetic study. Ab initio calculations confirm the high magnetic anisotropy of the system and allow determination of the direction of the easy-axis. The broken symmetry DFT calculations support the ferromagnetic intrachain interactions. The energetic relations relevant for relaxations are discussed. It is concluded that the magnetic model of [Co(NCS)2(py)2]n is not a pure Ising but the transversal exchange plays a role.

Mainly because of the large number of people affected and associated significant health policy implications, the Robert Koch Institute (RKI) is developing a public health surveillance system using diabetes as an example. In a first step to ensure long-term and comparable data collection and establish efficient surveillance structures, the RKI has defined a set of relevant indicators for diabetes surveillance. An extensive review of the available literature followed by a structured process of consensus provided the basis for a harmonised set of 30 core and 10 supplementary indicators. They correspond to the following four fields of activity: (1) reducing diabetes risk, (2) improving diabetes early detection and treatment, (3) reducing diabetes complications, (4) reducing the disease burden and overall costs of the disease. In future, in addition to the primary data provided by RKI health monitoring diabetes surveillance needs to also consider the results from secondary data sources. Currently, barriers to accessing this data remain, which will have to be overcome, and gaps in the data closed. The RKI intentends to continuously update this set of indicators and at some point apply it also to further chronic diseases with high public health relevance.

The new tritopic triaminoguanidine-based ligand 1,2,3-tris[(pyridine-2-ylmethylidene)amino]guanidine (H2pytag) was synthesized. The reaction of a mixture of cobalt(II) chloride and cobalt(II) perchlorate with the ligand H2pytag in pyridine solution leads to the formation of the trinuclear cobalt(II) complex [Co3(pytag)(py)6Cl3]ClO4. Three octahedrally coordinated high-spin cobalt(II) ions are linked through the bridging triaminoguanidine backbone of the ligand leading to an almost equilateral triangular arrangement. The magnetic properties of the complex were investigated by magnetic measurements, variable-temperature, variable-field magnetic circular dichroism (MCD) spectroscopy, and density functional theory as well as ab initio calculations. A rather strong antiferromagnetic exchange interaction between the cobalt(II) centers of ca. −12 cm–1 is determined together with a strong local anisotropy. The single-ion anisotropy of all three cobalt(II) centers is found to be easy-plane, which coincides with th...

SUMMARYA monitoring study was carried out in Gumara watershed, upper Blue Nile basin, with the objective of evaluating livestock water productivity (LWP) using a life cycle assessment method. Sixty two smallholder farmers were selected for the study implemented between November 2006 and February 2008. Data on crop and livestock production were collected to allow assessment of livestock water productivity. Study sites were situated in three different rainfed mixed crop/livestock farming systems; barley/potato based system (BPS), tef/finger-millet based system (TMS), and rice/noug based system (RNS). LWP was found to be significantly lower (p < 0.01) in RNS (0.057 USD m−3 water) than in TMS (0.066 USD m−3 water) or in BPS (0.066 USD m−3 water). Notably, water requirement per kg live weight of cattle increased towards the lower altitude area (in RNS) mainly because of increased evapo-transpiration. As a result, 20% more water was required per kg live weight of cattle in the low ground RNS compared to BPS situated in the upstream parts of the study area. Cattle herd management that involved early offtake increased LWP by 28% over the practice of late offtake. Crop water productivity expressed in monetary units (0.39 USD m−3 water) was higher than LWP (0.063 USD m−3 water) across the mixed farming systems of Gumara watershed. Strategies for improving LWP, from its present low level, could include keeping only the more productive animals, increasing pasture productivity and linking production to marketing. These strategies would also ease the imbalance between the existing high livestock population and the declining carrying capacity of natural pasture.

The synthesis, structure, and magnetic properties of two mononuclear cobalt(ii) complexes [Co(LSal,2-Ph)2] (1) and [Co(LNph,2-Ph)2] (2) are reported. The utilized sterically demanding Schiff-base ligands HLSal,2-Ph (2-(([1,1'-biphenyl]-2-ylimino)methyl)phenol) and HLNph,2-Ph (1-(([1,1'-biphenyl]-2-ylimino)methyl)naphthalen-2-ol) lead to a strong distortion of the [N2O2] coordination environment in the complexes 1 and 2, which can be primarily attributed to the variation in the dihedral angle between the planes of the two chelate ligands. Magnetic susceptibility and FD-FT THz-EPR measurements as well as ab initio calculations reveal that both complexes exhibit an easy-axis type of anisotropy. For both compounds frequency-dependent ac susceptibility measurements show an out-of-phase susceptibility under applied static fields of 400 and 1000 Oe. A detailed analysis of the underlying relaxation process is given, revealing significant differences in the contributions of Orbach, Raman, and direct processes within the observed temperature range. Fitting of the magnetic data leads to a spin-reversal barrier of 49 cm-1 for 1 at an applied field of 1000 Oe. For 2 the barrier is not well defined by the analysis of the relaxation times and is, therefore, approximated by the experimental barrier derived from FD-FT THz-EPR measurements (62.8 cm-1). The results from ab initio calculations and FD-FT THz-EPR measurements show that the distortion of the coordination sphere in complexes 1 and 2 from the pseudotetrahedral towards a square-planar coordination geometry leads to an increase in both the axial (D) and the rhombic zero-field splitting (E).

Reaction of cobalt(II) and nickel(II) thiocyanate with ethylisonicotinate leads to the formation of [M(NCS)2(ethylisonicotinate)2]n with M = Co (2-Co) and M = Ni (2-Ni), which can also be obtained by thermal decomposition of M(NCS)2(ethylisonicotinate)4 (M = Co (1-Co), Ni (1-Ni)). The crystal structure of 2-Ni was determined by single crystal X-ray diffraction. The Ni(II) cations are octahedrally coordinated by two N and two S bonding thiocyanate anions and two ethylisonicotinate ligands and are linked by pairs of anionic ligands into dimers, that are connected into layers by single thiocyanate bridges. The crystal structure of 2-Co was refined by Rietveld analysis and is isostructural to 2-Ni. For both compounds ferromagnetic ordering is observed at 8.7 K (2-Ni) and at 1.72 K (2-Co), which was also confirmed by specific heat measurements. Similar measurements on [Co(NCS)2(4-acetylpyridine)2]n that exhibits the same layer topology also prove magnetic ordering at 1.33 K. Constrained DFT calculations (CDFT) support the ferromagnetic interactions within the layers. The calculated exchange constants in 2-Ni were used to simulate the susceptibility by quantum Monte Carlo method. The single-ion magnetic anisotropy of the metal ions has been investigated by CASSCF/CASPT2 calculations indicating significant differences between 2-Ni and 2-Co.

Four new triphenylamine ligands with different substituents in the para position and their corresponding copper(II) complexes are reported. This study includes their structural, spectroscopic, magnetic, and electrochemical properties. The complexes possess a dinuclear copper(II) paddle‐wheel core, a building unit that is also common in metal‐organic frameworks. Electrochemical measurements demonstrate that the triphenylamine ligands and the corresponding complexes are susceptible to oxidation, resulting in the formation of stable radical cations. The square‐wave voltammograms observed for the complexes are similar to those of the ligands, except for a slight shift in potential. Square‐wave voltammetry data show that, in the complexes, these oxidations can be described as individual one‐electron processes centered on the coordinated ligands. Spectroelectrochemistry reveals that, during the oxidation of the complexes, no difference can be detected for the spectra of successively oxidized species. For the absorption bands of the oxidized species of the ligands and complexes, only a slight shift is observed. ESR spectra for the chemically oxidized complexes indicate ligand‐centered radicals. The copper ions of the paddle‐wheel core are strongly antiferromagnetic coupled. DFT calculations for the fully oxidized complexes indicate a very weak ferromagnetic coupling between the copper ions and the ligand radicals, whereas a very weak antiferromagnetic coupling is found among the ligand radicals.

The Front Cover shows a scene illustrating the need to investigate the properties of building blocks for complex systems to enable the basic design of new functional materials. It shows a model of the investigated paddle‐wheel complexes with copper‐bonded triphenylamines. Both paddle‐wheel units and triarylamine linkers are basic constituents found in several frameworks such as the networks shown in the image. More information can be found in the Full Paper by O. Akintola et al. on page 266 in Issue 3, 2019 (DOI: 10.1002/open.201800243).

Although water is a renewable natural resource, it has become insufficient at the global level. Unless the current efficiency level of water use can be increased, the trend of water shortages will become more serious. Among agricultural activities, livestock production is mostly considered an intensive water consuming operation although the knowledge and information related to livestock-water interaction appears to be limited in scope. The present review focused on the livestock-water interaction with the following objectives: 1) to strengthen the current understanding of the concept of livestock water productivity and relate it to life cycle assessment analysis framework; 2) to provide insights on the methodology of livestock water productivity estimation using water foot printing approach; 3) to assess the potential integrative intervention options towards improving livestock water productivity pertinent to the contexts of rain fed mixed farming. The concept of water accounting for livestock production is reviewed to reflect feasible options for improving animal productivity, income, livelihood and ecological benefits per unit of water input, especially the practical implications of these options for the rural poor in Sub-Saharan Africa. Utilising the rainfed mixed farming endowment as a relatively less competitive water scenario is also emphasised. In line with the intention for increased livestock water productivity, the likelihood of its negative impact on the environment and possible mitigating methods are outlined.

The endothelium regulates vascular function by releasing the vasodilator autacoid nitric oxide (NO) and the vasoconstrictor peptide endothelin-1 (ET-1). Impaired activity of NO as well as excessive activity of ET-1 have been demonstrated in hypercholesterolemia and atherosclerosis. Because dietary L-arginine can restore NO function and improve abnormal endothelium-dependent relaxation in hypercholesterolemic rabbits, we examined the effects of dietary supplementation with L-arginine in cholesterol-fed rabbits on endothelium-dependent vascular relaxation and ET-1-induced vascular contraction, as well as the systemic synthesis of ET-1. Rabbits were initially fed a diet enriched with 1% cholesterol for 4 weeks, followed by 0.5% cholesterol alone or supplemented with 2% L-arginine in drinking water during the next 12 weeks. Cholesterol feeding impaired endothelium-dependent relaxation of rabbit aortic rings ex vivo and increased urinary immunoreactive ET-1 excretion, along with decreased urinary nitrate excretion, an index of NO production. L-Arginine partially restored endothelium-dependent relaxation in parallel to increased urinary nitrate excretion and decreased urinary immunoreactive ET-1 excretion. Selective inhibition of ET-A receptors with BQ123 partially restored endothelium-dependent relaxation in hypercholesterolemic rabbits but had no effect on arterial rings from rabbits supplemented with L-arginine or from control animals. The contractile vascular response of aortic rings to exogenous ET-1 was increased in rabbits fed a high-cholesterol diet; this enhanced contractility to ET-1 was completely reversed by L-arginine. These data suggest that L-arginine restores endothelial function and normalizes the synthesis and vasoconstrictor response to ET-1 in hypercholesterolemia.

Objectives : l-arginine exerts anti-atherosclerotic effects in hypercholesterolaemic rabbits via modulating endogenous NO production. We investigated whether l-arginine inhibits thromboxane formation in vivo and platelet aggregation ex vivo in this animal model. Methods : The urinary excretion rates of 2,3-dinor-6-keto-PGF1α (major urinary metabolite of PGI2) and 2,3-dinor-TXB2 (major urinary metabolite of thromboxane A2) were used as indicators of platelet–endothelial cell interactions in vivo. Rabbits were fed 1% cholesterol (Cholesterol group, N =8), 1% cholesterol plus 2,25% l-arginine (Cholesterol+l-arginine, N =8), or normal rabbit chow (Control, N =4) for 12 weeks. Urine samples were collected in weekly intervals. At the end of the study period platelet aggregation ex vivo and endothelium-dependent and -independent vascular function of isolated aortic rings in vitro was assessed. Results : Urinary 2,3-dinor-TXB2 excretion significantly increased in the cholesterol group ( p

Background We investigated whether l -arginine induces regression of preexisting atheromatous lesions and reversal of endothelial dysfunction in hypercholesterolemic rabbits, whether similar effects can be obtained by cholesterol-lowering therapy with lovastatin, and which mechanism leads to these effects. Methods and Results Rabbits were fed 1% cholesterol for 4 weeks and 0.5% cholesterol for an additional 12 weeks. Two groups of cholesterol-fed rabbits were treated with l -arginine (2.0% in drinking water) or lovastatin (10 mg/d) during weeks 5 through 16. Systemic nitric oxide (NO) formation was assessed as the urinary excretion rates of nitrate and cGMP in weekly intervals. Cholesterol feeding progressively reduced urinary nitrate excretion to ≈40% of baseline ( P l -arginine reversed the reduction in plasma l -arginine/ADMA ratio and partly restored urinary excretion of nitrate and cGMP (each P l -Arginine completely blocked the progression of carotid intimal plaques, reduced aortic intimal thickening, and preserved endothelium-dependent vasodilator function. Lovastatin treatment reduced plasma cholesterol by 32% but did not improve urinary nitrate or cGMP excretion or endothelium-dependent vasodilation. Lovastatin had a weaker inhibitory effect on carotid plaque formation and aortic intimal thickening than l -arginine. l -Arginine inhibited but lovastatin potentiated superoxide radical generation in the atherosclerotic vascular wall. Conclusions Dietary l -arginine improves NO-dependent vasodilator function in cholesterol-fed rabbits and completely blocks the progression of plaques via restoration of NO synthase substrate availability and reduction of vascular oxidative stress. Lovastatin treatment has a weaker inhibitory effect on the progression of atherosclerosis and no effect on vascular NO elaboration, which may be due to its stimulatory effect on vascular superoxide radical generation.