Statins affect human iPSC-derived cardiomyocytes by interfering with mitochondrial function and intracellular acidification.

Statins are effective drugs in reducing cardiovascular morbidity and mortality by inhibiting cholesterol synthesis. These effects are primarily beneficial for the patient's vascular system. A significant number of statin users suffer from muscle complaints probably due to mitochondrial dysfunction, a mechanism that has recently been elucidated. This has raised our interest in exploring the effects of statins on cardiac muscle cells in an era where the elderly and patients with poorer functioning hearts and less metabolic spare capacity start dominating our patient population. Here, we investigated the effects of statins on human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-derived CMs). hiPSC-derived CMs were exposed to simvastatin, atorvastatin, rosuvastatin, and cerivastatin at increasing concentrations. Metabolic assays and fluorescent microscopy were employed to evaluate cellular viability, metabolic capacity, respiration, intracellular acidity, and mitochondrial membrane potential and morphology. Over a concentration range of 0.3-100 µM, simvastatin lactone and atorvastatin acid showed a significant reduction in cellular viability by 42-64%. Simvastatin lactone was the most potent inhibitor of basal and maximal respiration by 56% and 73%, respectively, whereas simvastatin acid and cerivastatin acid only reduced maximal respiration by 50% and 42%, respectively. Simvastatin acid and lactone and atorvastatin acid significantly decreased mitochondrial membrane potential by 20%, 6% and 3%, respectively. The more hydrophilic atorvastatin acid did not seem to affect cardiomyocyte metabolism. This calls for further research on the translatability to the clinical setting, in which a more conscientious approach to statin prescribing might be considered, especially regarding the current shift in population toward older patients with poor cardiac function.

Light-controlled bioelectrochemical sensor based on CdSe/ZnS quantum dots.

This study reports on the oxygen sensitivity of quantum dot electrodes modified with CdSe/ZnS nanocrystals. The photocurrent behavior is analyzed for dependence on pH and applied potential by potentiostatic and potentiodynamic measurements. On the basis of the influence of the oxygen content in solution on the photocurrent generation, the enzymatic activity of glucose oxidase is evaluated in solution. In order to construct a photobioelectrochemical sensor which can be read out by illuminating the respective electrode area, two different immobilization methods for the fixation of the biocatalyst have been investigated. Both covalent cross-linking and layer-by-layer deposition of GOD by means of the polyelectrolyte polyallylamine hydrochloride show that a sensor construction is possible. The sensing properties of this type of electrode are drastically influenced by the amount and density of the enzyme on top of the quantum dot layer, which can be advantageously adjusted by the layer-by-layer technique. By depositing four bilayers [GOD/PAH](4) on the CdSe/ZnS electrode, a fast-responding sensor for the concentration range of 0.1-5 mM glucose can be prepared. This study opens the door to multianalyte detection with a nonstructured sensing electrode, localized enzymes, and spatial read-out by light.

Origin of thalamic inputs to the primary, premotor, and supplementary motor cortical areas and to area 46 in macaque monkeys: a multiple retrograde tracing study.

The origin of thalamic inputs to distinct motor cortical areas was established in five monkeys to determine whether the motor areas receive inputs from a common thalamic nucleus and the extent to which the territories of origin overlap. To not rely on the rough definition of cytoarchitectonic boundaries in the thalamus, monkeys were subjected to multiple injections of tracers (four to seven) in the primary (M1), premotor (PM), and supplementary (SMA) motor cortical areas and in area 46. The cortical areas were distributed into five groups, each receiving inputs from a specific set of thalamic nuclei: 1) M1; 2) SMA-proper and the caudal part of the dorsal PM (PMdc); 3) the rostral and caudal parts of the ventral PM (PMvr and PMvc); 4) the rostral part of the dorsal PM (PMdr); and 5) the superior and inferior parts of area 46 (area 46sup and area 46inf). A major degree of overlap was obtained for the origins of the thalamocortical projections directed to areas 46inf and 46sup and for those terminating in SMA-proper and PMdc. PMvc and PMvr received inputs from adjacent and/or common thalamic regions. In contrast, the degree of overlap between M1 and SMA was smaller. The projection to M1 shared relatively limited zones of origin with the projections directed to PM. Thalamic inputs to the motor cortical areas (M1, SMA, PMd, and PMv), in general, were segregated from those directed to area 46, except in the mediodorsal nucleus, in which there was clear overlap of the territories sending projections to area 46, SMA-proper, and PMdc.

Dual morphology and topography of the corticothalamic terminals originating from the primary, supplementary motor, and dorsal premotor cortical areas in macaque monkeys.

In the motor, somatosensory, and auditory systems of rodents and cats, the corticothalamic connection is composed of a main projection formed by small endings and a minor projection terminating with giant endings. To establish whether the corticothalamic projection originating from motor cortical areas in primates exhibits the same duality, the anterograde tracer biotinylated dextran amine was injected in eight macaque monkeys in the primary motor (M1; n = 3), the supplementary motor (SMA; n = 3) and the dorsal premotor (PMd; n = 2) cortical areas to label corticothalamic axons. The corticothalamic projection originating from these three motor cortical areas was characterized by the presence of axon terminals constituting the same two types of endings, observed both as boutons en passant and terminaux. The population of small endings exhibited a mean cross-sectional maximum diameter of 0.95 microm (S.D. = 0.23), a range of diameters not overlapping that of giant endings (mean diameter = 3.46 microm, S.D. = 0.74 microm). Topographically, the giant endings originating from M1 were located in the same thalamic nucleus (ventroposterolateral nucleus, oral part) in which the small endings were found. In contrast, the giant endings originating from SMA and PMd were located in a thalamic nucleus (mediodorsal nucleus) distinct from the main termination zone formed by small endings. Along the rostrocaudal axis, the giant endings were distributed in a restricted zone, irrespective of the origin of the projection (M1, SMA, PMd). The dual morphology of corticothalamic endings, previously found in rodents and cats, is present in the motor system of subhuman primates for both primary and nonprimary motor cortical areas.

Direct visual pathways for reaching movements in the macaque monkey.

The brain seems to process the location of objects faster than their intrinsic features, such as size, when these parameters are used to guide action. To uncover a potential anatomical substrate of these different processing speeds, we investigated in the monkey the pathways linking extrastriate visual cortex with the dorsal premotor area, a frontal area known to be involved in visually guided reaching movements. Retrogradely transported anatomical tracers were injected at physiologically defined sites and the distribution of labelled cells was examined in the ipsilateral cortex. We found a projection to the dorsal premotor cortex from the parieto-occipital area (PO). This area receives direct projections from the primary visual cortex (V1), and is part of the dorsal visual stream involved in the processing of spatial information. No direct projections to the dorsal premotor cortex arise from the ventral visual areas, thought to process object features. Our finding provides evidence for direct pathways from the dorsal visual stream to the dorsal premotor cortex and supports the view that the location of objects is processed faster by the brain than their intrinsic features.

AIDS spreads eastward.

PIP: In just 3 months in 1991, WHO increased its estimate of the number of people infected with HIV in all of Asia 2 fold (500,000-1 million). By 2000, WHO estimated that there will be 250,000 new cases each year in India and Thailand alone where HIV infection has spread most rapidly. A professor from the All India Institute of Medical Sciences reported that AIDS is no longer restricted to the urban areas of Madras. Bombay, Calcutta, and Delhi. It spread to Manipur which is located on the border of the Golden Triangle, a drug trading area, where an especially high rate existed in the early 1990s. For example, in October 1989, 1 blood sample from this area tested positive for HIV, but by June 1990, 54% of 1500 blood samples tested positive. Thailand already had a serious AIDS epidemic so with a high HIV rate in Manipur, India and Thailand, AIDS could spread to Myanmar, Laos, Vietnam, and southern China. 1 major mode of HIV transmission in India is prostitution. Harsh economic conditions often force women into it. Often they are coerced. Since condom use has been promoted as a method of family planning, prostitutes have not considered using condoms to protect themselves and their clients from AIDS. An Indian sociologist advocated targeting truck drivers since the prostitutes do not have the power to demand safe sex and truck drivers spread it into rural areas. The Thailand, the number of HIV infected people climbed from 300,000 in December 1990 to 400,000 by mid 1991. Intravenous drug use, (males make up 90% of drug addicts) was the main mode of HIV transmission in Bangkok. These males than transmit HIV to prostitutes. In mid 1991, however, 92% of drug addicts in Bangkok practice safe injection techniques. Seroprevalence in diverse Thai groups included 6% of men with sexually transmitted diseases, 15% of prostitutes, and 6% of army recruits.^ieng

AIDS epidemic grows but response slows.

PIP: A brief note on the status of the AIDS pandemic, from the Amsterdam VIIIth International Conference on AIDS, warns that the course of the epidemic is not being altered by prevention efforts. AIDS occurs in every country, usually spread by heterosexual contact, so that women are equally affected with men. WHO estimates that there are 2 million cases as of mid-1992, and that there will be 15-18 million by 2000. 90% of the expected cases by 2000 will be in developing countries, particularly in Africa. HIV is particularly widespread in central African cities, affecting as many as 38% of young people in Kigali, Rwanda. While the epidemic is spreading, the response to prevention efforts has reached a plateau, with no more evidence of effect from existing prevention programs. Unfortunately AIDS is being followed by an epidemic of tuberculosis. AIDS preferentially attacks the marginalized, stigmatized, and those of lesser status, such as women. In the US there are still 47,500 new cases annually, most in the South, and among blacks and Hispanics. Most Americans do not perceive themselves at risk, and ignore their cumulative lifetime risk.^ieng