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Query: UMLS:C0267964 (
PAA
)
2,561
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Using enzyme-linked immunoblot technique (ELIB), the antigenic protein components of
water
-soluble and urea-soluble antigens of Schistosoma japonicum eggs (JSEA, JEAU) and Paragonimus westermani adult worms (
PAA
,
PAA
-U) were analysed. The results showed that in both JSEA and JEA-U, 8 and 3 bands of polypeptides could be recognized by sera from patients with schistosomiasis japonica (Sj). In both
PAA
and
PAA
-U, there were 9 and 2 bands of polypeptides respectively, which could be recognized by sera from patients with pagumogonimiasis skrjabini (Ps). The components of 36/37kDa in
PAA
and 20/21 kDa in JSEA were identified to be shared antigenic fractions existing between the two species of trematodes, which gave positive reaction against patient's sera from both S.j. and P.s., while
PAA
-U caused the reaction only with sera from patients with acute schistosomiasis.
PAA
-U might be useful to avoid cross reaction in the majority of schistosomiasis patients in the fields.
...
PMID:[Common antigenic components in soluble antigens shared by Schistosoma japonicum eggs and Paragonimus westermani adult worms]. 206 50
A syndrome of sleep apnoea may appear 15 to 29 years after acute anterior poliomyelitis (
PAA
). It is generally a mixed syndrome with an association of central type and obstructive apnoea in variable proportions. We report such a case occurring in a patient who had presented 30 years before with
PAA
, and presenting on this occasion with resting pulmonary artery hypertension, polycythaemia but without disturbance of blood gases. Treatment with positive pressure ventilation was given by the nasal route at 10 cm of
water
leading to an improvement with a significant decrease in the number and duration of apnoeic episodes and a disappearance of desaturation. The sleep apnoea syndrome (SAS) should be considered as a possible late sequel of
PAA
.
...
PMID:[Sleep apnea syndrome: late sequela of poliomyelitis]. 318 71
The oral administration of a suspension of N-phenylanthranilic acid (N-PAA), over the range of 0.5 to 2 mmol/kg for 14 consecutive days, caused a dose-related renal papillary necrosis (RPN), which involved no more than 30% of the medullary apex. This area of necrosis was no greater following daily doses of 3 and 5 mmol/kg of N-
PAA
for 14 days, but cortical degenerative changes were induced. The area of the necrotic lesion was greater in the left kidneys of individual rats than in the right kidneys. The apex-limited histopathological changes associated with the administration of low doses of N-
PAA
were not reflected by altered electrolyte or
water
homeostasis and only high doses of N-
PAA
caused significant changes. Urinary volume was significantly increased (in animals treated with 5 mmol/kg), whereas urinary osmolality (greater than 2 mmol/kg N-PAA), and Na+ (5 mmol/kg), K+ (5 mmol/kg), and Cl- (5 mmol/kg) excretion was decreased compared to controls. Blood urea nitrogen was increased at doses greater than 3 mmol/kg in association with cortical degenerative changes. When untreated rats were dosed orally with NH4Cl (400 mg/kg) there was a lag period between 0 and 2 hr (when no changes in H+ excretion occurred), but the urinary pH was depressed in the 2- to 4-hr collection period. Only those rats treated with the highest dose of N-
PAA
(5 mmol/kg) showed a significantly impaired urinary acidification after NH4Cl loading. There was, however, a statistically significant dose-related decrease in the excretion of Cl- following NH4Cl dosing, provided urine was sampled between 0 and 2 hr. These data highlight the failure of the commonly used renal function tests (such as urinary volume, osmolality, and electrolyte excretion) to reflect apex-limited RPN, unless cortical degenerative changes were also present. The dose-related depression of Cl- excretion in the 0- to 2-hr period following oral NH4Cl loading, suggests that appropriately timed sampling of this urinary anion could offer an improved criterion for the diagnosis of RPN.
...
PMID:The effect of N-phenylanthranilic acid-induced renal papillary necrosis on urinary acidification and renal electrolyte handling. 647 61
Polyacrylic acid-IgG polymer (PAA-IgG) activates the classical and alternative pathway of complement as shown by specific Clq-(IgG-PAA) interaction and the generation of C4d, Bb, C3b, C3a and C5a. This
water
soluble and stable
PAA
-IgG polymer represents a model substance for the study of humoral and cellular inflammatory mechanisms, mediated by the complement system.
...
PMID:The synthesis of a water soluble complement activating polyacrylic acid-IgG polymer. 794 74
A cationic, high-
water
-content hydrogel membrane composed of poly(vinyl alcohol) (PVA) and poly(ally-biguanido-co-allylamine) hydrochloride (PAB) with positively charged biguanido groups that resemble arginine residues was developed. The PAB was prepared by reacting poly(allylamine) hydrochloride (
PAA
) with guanyl-O-methyl isourea. PAB/PVA hydrogel membranes were prepared by repeated freezing and thawing. For comparison, hydrogel membranes composed of
PAA
and PVA were also prepared. The interaction between these hydrogel membranes and mouse fibroblast (L929) was studied by a cell culture method. The PAB hydrogel blend had a relatively low percentage of initial cell attachment. The cell growth on the PAB hydrogel membranes showed a maximum at 5 mol % PAB content that was as high as commercially available plastic films. However, cells on hydrogel membranes with 50 mol % PAB content and 0 mol % PAB content (only PVA) did not seem to grow; neither did the 5/95
PAA
/PVA membranes.
Water
contact angles of hydrogel membranes did not vary with the PAB content. Morphology of the cell attachment was observed by SEM. On the PAB blend hydrogel surfaces, cells were not spindle-shaped and monolayers, but rather cells aggregated in spherical clusters.
...
PMID:Cell growth on poly(vinyl alcohol) hydrogel membranes containing biguanido groups. 800 50
The ability of four different 40% poly(acrylic acid) (
PAA
) solutions, containing 4 or 6 wt-% of either Na2SO4 or (NH4)2SO4, to cause precipitation of CaSO4 on dentin surfaces was investigated. Each treatment consisted of exposing the dentin to one of the four solutions for either 1 or 2 min and was followed by a
water
rinse (1 min) and air drying (30 sec). The treated dentin surfaces were then evaluated in a scanning electron microscope (SEM), which showed that crystals precipitated on the dentin with these solutions. Of the four investigated PAAs, one performed better than the others with regard to crystal precipitation and blockage of the tubules. This solution was selected for additional studies of the effects of different
PAA
concentrations (10%, 20%, 30%, 40%, and 50%). In these solutions, 4 and 6 wt-% of either Na2SO4 or (NH4)2SO4 were dissolved. Additional dentin surfaces were then treated with these solutions as described earlier and evaluated in an SEM. This evaluation showed that solutions containing 30-50%
PAA
resulted in optimized crystal formation for all the different sulfate solutions and that the optimization occurred within 1 min. Besides optimizing crystal precipitation, these mixtures also minimized the frequency of open dentinal tubules.
...
PMID:Crystal precipitation on dentin by poly(acrylic acid) solutions containing SO4(2-) ions. 830 12
The immunogenic properties of
water
soluble (
PAA
-Cu(2+)-BSA) and colloidal (
PAA
-Cu(2+)-BSA.P) polycomplexes were investigated, and the specificity of antibodies produced was analyzed. Polycomplexes containing progesterone appeared to possess a high steroid-specific immunogenic activity. A comparative study of immunogenic properties of polycomplexes versus BSA.P + incomplete Freund's adjuvant (IFA) mixtures revealed differences in regards to the specificity of antibody production. In contrast to the IFA system, polycomplexes were able to generate P- as well as BSA-specific antibodies. Such a response is determined, possibly, by increases in the immunogenicity of weak antigenic determinants on the surface of protein globules and or by the representation of dormant determinants existing in the miner site upon complex formation with polyelectrolytes. Finally, using a short immunization procedure based on use of
PAA
-Cu(2+)-BSA polycomplexes, we produced seven monoclonal antibodies against progesterone included in polyelectrolyte complexes with affinities Kd ranging between 1.3 x 10 (-5) and 9 x 10(-8) M.
...
PMID:Immune response to progesterone involved in Cu(2+)-mediated polyanion-protein complex--antigen specificity and affinity of hybridoma clones. 890 97
The pH-dependent complexation of poly(acrylic acid) (
PAA
) with phospholipid (phosphatidylcholine) vesicles was characterized by fluorescence polarization, differential scanning calorimetry (DSC), and surface pressure measurements of phospholipid monolayers. The complexation was pronounced below pH 4, when the polymer carboxyl groups are protonated, as shown by the binding of
PAA
to vesicles and the decrease in polymer mobility. The complexation was strong at low polymer concentrations and was weaker at higher polymer concentrations.
PAA
complexation increased the gel to liquid crystalline (LC) phase transition temperature (Tm) and enthalpy (DeltaH) of the vesicles accompanied by a decrease in the transition cooperativity. This is most likely due to perturbations in the phospholipid headgroup upon
PAA
interaction. The effect of polymer adsorption on the phospholipid surface was investigated at the phospholipid/
water
interface. The ability of
PAA
to penetrate between the phospholipid molecules as a function of pH was determined by the lateral expansion of the monolayer at a constant surface pressure. The ability of the polymer to penetrate into the monolayer increased with decreasing pH. These results suggest that
PAA
complexation leads to expansion of the phospholipid packing of the vesicles by altering the phospholipid headgroup conformation.
...
PMID:Characterization of pH-Dependent Poly(acrylic Acid) Complexation with Phospholipid Vesicles 905 34
Mouse epidermal growth factor (EGF) was covalently conjugated with the
water
-soluble polymer, poly(acrylic acid) (EGF-
PAA
), or with the
water
-insoluble polymer, surface-hydrolyzed poly(methyl methacrylate) (EGF-PMMA). Immobilized EGF (EGF-PMMA) stimulated DNA synthesis in Chinese hamster ovary cells overexpressing EGF receptors in amounts that were 5 to 10% of those of free EGF required for comparable effects. In addition, the maximal mitogenic effect of EGF-PMMA was greater than that of unconjugated EGF or EGF-
PAA
. EGF, EGF-
PAA
, and EGF-PMMA induced the autophosphorylation of EGF receptors and the stimulation of mitogen-activated protein kinase. However, whereas the onset of these effects was delayed with EGF-PMMA, they persisted for much longer than those of EGF and EGF-
PAA
. Unlike EGF and EGF-
PAA
, EGF-PMMA was not associated with cells after their removal from culture and did not induce receptor internalization. Culturing cells with PMMA-immobilized EGF thus represents a model system for studying "juxtacrine" stimulation of cells by membrane-bound growth factors.
...
PMID:Enhancement of the mitogenic effect by artificial juxtacrine stimulation using immobilized EGF. 913 20
To investigate whether plasma sodium pump inhibitory activity is controlled by cardiopulmonary and aortic baroreceptors, mean arterial pressure, right atrial pressure, sodium and
water
balances, plasma renin activity, plasma aldosterone concentration and plasma antinatriferic activity (
PAA
; plasma sodium pump inhibitory activity) were determined before, during and after Ringer volume expansion (10% of body wt) in anaesthetized dogs. Animals were studied with intact reflexes (CTR, n = 7) and after acute cervical bilateral vagosympathetic denervation (VGT, n = 8). With the exception of
PAA
, none of the parameters were different between groups before, during or after Ringer volume expansion. The
PAA
(microA cm-2) was similar for both groups before expansion and before either sham (CTR) or vagosympathectomy (VGT) was performed (CTR = 3.6 +/- 0.4 vs. VGT = 4.3 +/- 0.3). Compared to baseline,
PAA
at the end of the volume expansion phase increased in both groups (CTR = 6.1 +/- 0.8, P < 0.05; VGT = 9.1 +/- 0.7, P < 0.0005); however, this
PAA
value was significantly greater in the VGT group than in the CTR group (P < 0.01). At the end of the post-expansion phase,
PAA
levels returned toward baseline in both groups (CTR = 4.4 +/- 0.5 vs. VGT = 4.8 +/- 0.2; n.s. vs. baseline); however, this
PAA
value in the CTR group was not significantly different from its pak value. The present data confirm that
PAA
is increased in response to saline volume expansion, and suggest that
PAA
synthesis and/or release is under inhibitory vagosympathetic control during saline volume expansion.
...
PMID:Enhanced increase of plasma sodium pump inhibitory activity to saline expansion in vagosympathectomized and anaesthetized dogs. 917 17
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