3- and 5-isoxazolol zwitterions: an ab initio molecular orbital study relating to GABA agonism and antagonism

The Hartree-Fock ab initio molecular orbital method has been applied to eight compounds: GABA (gamma-amino butyric acid) (1), its partially rigidified analog, TACA (trans-4-aminocrotonic acid) (2), six isoxazolol analogs; muscimol (5-aminomethylisoxazol-3-ol (3), THIP (4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3-ol) (4), THAZ (5,6,7,8-tetrahydro-4H-isoxazolo[4,5-d]azepin-3-ol) (5), isomuscimol (3-aminomethylisoxazol-5-ol) (6), iso-THIP (4,5,6,7-tetrahydroisoxazolo[3,4-c] pyridin-5-ol) (7), and iso-THAZ (5,6,7,8-tetrahydro-4H-isoxazolo[3,4-d]azepin-5-ol) (8). GABA is an endogenous inhibitory transmitter. The four following molecules (2), (3), (4) and (5) are agonist: they bind themselves to the GABA receptors and induce approximately the same effect as GABA. (6) is lightly agonist, presenting a lower affinity. Compounds (7) and (8) are antagonists, giving rise to convulsion. Optimized molecular conformations of GABA (1), muscimol (3) and isomuscimol (6) are discussed. Geometric and electronic parameters showing the presence of intramolecular hydrogen bonds are presented. The permutation of the heteroatoms in the isoxazole ring has no effect on the side-chain orientation explaining maybe the agonist character of isomuscimol, being able to adopt easily and exactly the active conformation. Atomic charge distributions and electronic overlap populations for all compounds have been computed in order to try to understand why their GABAergic activities can be so different. The computed values show that the 3-isoxazolol ring mimics in a good way the carboxylic function of GABA. They also illustrate the larger electronic delocalization within the 5-isoxazolol ring and therefore the resulting antagonist character, except for isomuscimol.     

Front Cover: Photoacoustic imaging of the human placental vasculature (J. Biophotonics 4/2020)

Successful therapy of twin‐to‐twin transfusion syndrome requires accurate imaging to guide laser photocoagulation of the anastomosing placental vessels. Photoacoustic (PA) imaging is an alternative imaging method that provides contrast for hemoglobin, and in this study, it was used to visualize chorionic superficial and subsurface vasculature in human placentas. The strong potential of PA imaging to guide minimally invasive fetal therapies was demonstrated. Further details can be found in the article by Efthymios Maneas, Rosalind Aughwane, Nam Huynh, et al. ( e201900167 ).

     

Alkaloids of Alstonia plumosa

Nineteen indole alkaloids have been isolated from the root and stem barks of Alstonia plumosa, from New Caledonia. Twelve of them were known compou     

Interaction of phospholipids (Lysophosphatidylethanolamines) with water and sodium cation

We have performed detailed ab initio SCF calculations on the intermolecular interaction energies for one Na⁺ ion and one water molecule with two molecular fragments, one exemplifying a phospholipid (PL) head (PLHD) and the other, a phospholipid tail (PLTL). A 6-12-1 atom-atom pair potential for the interaction of a Na⁺ ion and water with a lysophosphatidyl-ethanolamine (LPEA) was derived from these results by a fitting procedure. This fitted potential was used to obtain isoenergy maps that provide energy profiles of the Na⁺ ion and the water around the phospholipids. The interaction of the Na⁺ ion with PL, as well as the interaction of water with the PL, can be visualized from these maps, which, as expected, show regions of hydrophilicity and hydrophobicity for the water and indicate a very strong binding site for the Na⁺ ion on the phosphate. It appears to be a stationary site that would limit the Na⁺ ion mobility. This binding site is located near the double-bonded oxygen atom of the phosphate group; its binding energy for Na⁺ is 67 kcal/mol. On the other hand the NH⁺ group of PLHD ahows strong electrostatic repulsion of Na⁺ while interacting with water with a binding energy of 13 kcal/mol. This potential energy well region for water is separated from another of similar depth near the phosphate by a barrier and both regions are expected to act as binding sites for water.     

Age effects and secular trend in a cross-sectional sample: application to four head dimensions in Belgian adults

If longitudinal studies represent the more direct way to analyze modifications resulting from aging, often for obvious reasons cross-sectional samples can also be used for this purpose. But in this case differences between age groups cannot be identified with the effects of age only; they can also be attributed to the effects of a secular trend. It is the aim of this study to show, using four cephalic dimensions and a cross-sectional sample, the need to take into account the effect of a secular trend when the age effect is studied. In 1985 a study of head and facial measurements of 182 Belgian men, aged 25-54 years, was carried out. A simple comparison between different age groups (F tests) revealed significant differences for head breadth and facial breadths. However, no difference for head length was observed. The amplitude of the secular trend in the Belgian population is already known; thus an easy calculation is proposed to define the effects of the age factor. For head breadth the whole difference seems to be the result of the important decrease of secular trend, whereas the global increase observed for the bizygomatic and bigonial breadths results in part from the decrease resulting from the secular trend and in part from the increase resulting from the age effect.