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Revista Cubana de Investigaciones Biomédicas

ISSN 1561-3011 (Electronic)
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2019, Number 1

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Rev Cubana Invest Bioméd 2019; 38 (1)

Kinetics-like equation for cerebrospinal fluid-blood diffusion models

Rodríguez-Pérez JA, Mirabal-Viel A, Pérez-del-Vallín V, Meijides-Mejías C, Castillo-González W, Lumpuy-Castillo J, Dorta-Contreras AJ
Full text How to cite this article

Language: English
References: 6
Page: 1-7
PDF size: 325.82 Kb.


Key words:

cerebrospinal fluid-blood, Q albumin, proteins.

ABSTRACT

Introduction: The diffusion of proteins from the blood to the cerebrospinal fluid is influenced by its molecular weight and by the intrinsic properties and biological properties of the protein.
Methods: Paired samples of serum and cerebrospinal fluid were taken from normal subjects to quantify albumin and proteins of the lectin pathway of the complement system. The distribution of these with regard to the value of QAlbúmin = (Albumin in serum/albumin in cerebrospinal fluid) was evaluated because this protein is used as a marker of the passage of the barrier.
Results: It was observed that some of these describe a saturation pattern which resembles the curves that describe the Michaelis-Menten reaction of enzymatic activity. This led to the consideration of two constants that will help to characterize the behavior of these proteins by spreading to the cerebrospinal fluid: the maximum Q of the protein, which is the maximum proportion found empirically between the concentrations in blood and cerebrospinal fluid and the value Kcdw which is the value of the average diffusion speed of Q albumin when the semi-maximal value of the Q of the protein under study is obtained.
Conclusions: Empirically obtained constants will help the characterization and differentiation of the diffusion of these new proteins as they pass from the blood to the cerebrospinal fluid.


REFERENCES

  1. Pihl R, Jensenius JC, Thiel S. MASP-2. The Complement Facts Book. Academic Press 2018: p. 79-87.

  2. Yaseen S, Demopulos G, Dudler T, Yabuki M, Wood C L, Cummings W J, Tjoelker L, et al. Lectin pathway effector enzyme mannan-binding lectin-associated serine protease-2 can activate native complement C3 in absence of C4 and/or C2 . The FASEB Journal 2017 31:5,2210-2219

  3. Dorta-Contreras A J, Padilla-Docal B, Iglesias González I M, Martínez-Larrarte J P, Castillo-González W, González-Losada C, González-Argote J, et al. MAp44: diffusion from blood to cerebrospinal fluid and intrathecal synthesis . The FASEB Journal 2016 30:1_supplement, 970.1-970.1

  4. Degn SE, Jensen L, Gál P, Dobó J, Holmvad SH, Jensenius JC, et al. Biological variations of MASP-3 and MAp44, two splice products of the MASP1 gene involved in regulation of the complement system. J Immunol Methods 2010;361:37-50.

  5. Dorta-Contreras A J, Padrón-González A A, González-Losada C, Lumpuy-Castillo J, Rodriguez-Pérez J A, Ramos-Robledo A, Martínez-Reyes J, et al. MASP-3: a new leptomeningeal protein in the lectin pathway. The FASEB Journal 2018 32:1_supplement, 741.5-741.5

  6. Padrón-González AA, González-Losada C, Lumpuy-Castillo J, Rodriguez-Pérez J A, Ramos-Robledo A, Castillo-González W, Dorta-Contreras A J. MASP-3 aggregation and its blood to cerebrospinal fluid diffusion. The FASEB Journal 2018 32:1_supplement, 741.1-741.1




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Rev Cubana Invest Bioméd. 2019;38