DESIGNING URBAN SPACES ACCORDING TO EARTH ENERGYSTRUCTURE: TOWARD A BETTER LIVE IN CITIES

Architecture was and still a vital need in our life; in very ancient times, it represented a human’s shelter from his surroundings. Architecture then along became the source of the human comfort along with the progress of the civilizations. To achieve that human comfort it was necessary for architecture to react harmoniously with its environment. Therefore, certain considerations like Social, constructional, environmental have been assigned to Architecture. Modern architecture has neglected a natural inevitable consideration: The Earth\u27s Energy which is a natural electromagnetic field of the Earth, resulting from of the melted iron in the earth\u27s core. That energy have many types and formation, such as Lines, Grids, spots…etc. Modern researches proved that each type affecting Humans and the Environment differently. The human body also has many kinds of energy. Modern science defines the energy of the human body as an electromagnetic field that surrounds and penetrates it. Therefore, there is a continuous interaction between humans and the earth. This research intended to focus on and demonstrate the Earth\u27s Energy types and formations, and measurements used tools. In addition, the research suggesting a methodology of Designing Urban Spaces according to the Earth’s Energy structure in the site, to provide better lives in Cities

HIV-Tat Exacerbates the Actions of Atazanavir, Efavirenz, and Ritonavir on Cardiac Ryanodine Receptor (RyR2)

The incidence of sudden cardiac death (SCD) in people living with HIV infection (PLWH), especially those with inadequate viral suppression, is high and the reasons for this remain incompletely characterized. The timely opening and closing of type 2 ryanodine receptor (RyR2) is critical for ensuring rhythmic cardiac contraction–relaxation cycles, and the disruption of these processes can elicit Ca2+ waves, ventricular arrhythmias, and SCD. Herein, we show that the HIV protein Tat (HIVTat: 0–52 ng/mL) and therapeutic levels of the antiretroviral drugs atazanavir (ATV: 0–25,344 ng/mL), efavirenz (EFV: 0–11,376 ng/mL), and ritonavir (RTV: 0–25,956 ng/mL) bind to and modulate the opening and closing of RyR2. Abacavir (0–14,315 ng/mL), bictegravir (0–22,469 ng/mL), Rilpivirine (0–14,360 ng/mL), and tenofovir disoproxil fumarate (0–18,321 ng/mL) did not alter [3H]ryanodine binding to RyR2. Pretreating RyR2 with low HIV-Tat (14 ng/mL) potentiated the abilities of ATV and RTV to bind to open RyR2 and enhanced their ability to bind to EFV to close RyR2. In silico molecular docking using a Schrodinger Prime protein–protein docking algorithm identified three thermodynamically favored interacting sites for HIV-Tat on RyR2. The most favored site resides between amino acids (AA) 1702–1963; the second favored site resides between AA 467–1465, and the third site resides between AA 201–1816. Collectively, these new data show that HIV-Tat, ATV, EFV, and RTV can bind to and modulate the activity of RyR2 and that HIV-Tat can exacerbate the actions of ATV, EFV, and RTV on RyR2. Whether the modulation of RyR2 by these agents increases the risk of arrhythmias and SCD remains to be explored

Additional file 4 of Mapping age- and sex-specific HIV prevalence in adults in sub-Saharan Africa, 2000–2018

Additional file 4: Supplemental results.1. README. 2. Prevalence range across districts. 3. Prevalence range between sexes. 4. Prevalence range between ages. 5. Age-specific district ranges