Central and systemic antidiuretic hormone and angiotensin II in salt and fluid balance of birds as compared to mammals

Role of plasma ANG II in the excretion of acute sodium load in a bird with salt glands (Anas platyrhynchos)

“…In addition, centrally applied ANG II stimulates the release of arginine vasotocin, the antidiuretic hormone of birds, as well as stimulating water intake (28). In addition, under conditions of dehydration (19) and hemorrhage (29), plasma ANG II concentrations rise, and during salt loading the levels decrease (15,18), providing further evidence that the physiological function of ANG II is to prevent extracellular fluid volume shrinkage, via antinatriuresis and antidiuresis.…”

Role of plasma ANG II in the excretion of acute sodium load in a bird with salt glands (Anas platyrhynchos)

“…In addition, centrally applied ANG II stimulates the release of arginine vasotocin, the antidiuretic hormone of birds, as well as stimulating water intake (28). In addition, under conditions of dehydration (19) and hemorrhage (29), plasma ANG II concentrations rise, and during salt loading the levels decrease (15,18), providing further evidence that the physiological function of ANG II is to prevent extracellular fluid volume shrinkage, via antinatriuresis and antidiuresis.…”

Central vasotocin-immunoreactive system in a male passerine bird (Junco hyemalis)

“…In birds, the physiological functions classically attributed to VT are the regulation of water and electrolytic balance (for reviews, see Simon Oppermann et al, 1988;Ramieri and Panzica, 1989) and of blood pressure (Szczepanska-Sadowska et al, 1985). Like VP in mammals, VT in birds is involved in the control of reproduction including oviposition (Rzasa and Ewy, 1982;Rice et al, 1985;Shimada et al, 1986;Koike et al, 1988), male sexual behavior (Kihlström and Danninge, 1972;Bernroider and Leutgeb, 1994;Leutgeb, 1995;Castagna et al, 1998;Goodson and Adkins-Regan, 1999) and aggressive behav-ior (Goodson, 1998a,b;Goodson and Adkins-Regan, 1999), and vocalizations (Voorhuis et al, 1991a;Castagna et al, 1998).…”

Distribution of AVT gene expressing neurons in the prosencephalon of Japanese quail and chicken

“…In birds, AVT is involved in the regulation of water and electrolyte balance (for reviews see Simon-Oppermann et al 1988;Ramieri and Panzica 1989), in thermoregulation (Hassinen et al 1994), in the regulation of blood pressure (SzczepanskaSadowska et al 1985), in oviposition (Rzasa and Ewy 1982;Rice et al 1985;Shimada et al 1986;Koike et al 1988), in some cognitive and adaptative activities (Davis et al 1982;Davis and Pico 1984) and in the activation of some aspects of reproductive behaviour (copulatory behaviour: Kihlström and Dannige 1972;singing behaviour: Voorhuis et al 1991;sexual motivation: Bernroider and Leutgeb 1994).…”

Role of plasma ANG II in the excretion of acute sodium load in a bird with salt glands (Anas platyrhynchos)

“…In addition, centrally applied ANG II stimulates the release of arginine vasotocin, the antidiuretic hormone of birds, as well as stimulating water intake (28). In addition, under conditions of dehydration (19) and hemorrhage (29), plasma ANG II concentrations rise, and during salt loading the levels decrease (15,18), providing further evidence that the physiological function of ANG II is to prevent extracellular fluid volume shrinkage, via antinatriuresis and antidiuresis.…”

Central vasotocin-immunoreactive system in a male passerine bird (Junco hyemalis)

“…In birds, the physiological functions classically attributed to VT are the regulation of water and electrolytic balance (for reviews, see Simon Oppermann et al, 1988;Ramieri and Panzica, 1989) and of blood pressure (Szczepanska-Sadowska et al, 1985). Like VP in mammals, VT in birds is involved in the control of reproduction including oviposition (Rzasa and Ewy, 1982;Rice et al, 1985;Shimada et al, 1986;Koike et al, 1988), male sexual behavior (Kihlström and Danninge, 1972;Bernroider and Leutgeb, 1994;Leutgeb, 1995;Castagna et al, 1998;Goodson and Adkins-Regan, 1999) and aggressive behav-ior (Goodson, 1998a,b;Goodson and Adkins-Regan, 1999), and vocalizations (Voorhuis et al, 1991a;Castagna et al, 1998).…”

Distribution of AVT gene expressing neurons in the prosencephalon of Japanese quail and chicken

“…In birds, AVT is involved in the regulation of water and electrolyte balance (for reviews see Simon-Oppermann et al 1988;Ramieri and Panzica 1989), in thermoregulation (Hassinen et al 1994), in the regulation of blood pressure (SzczepanskaSadowska et al 1985), in oviposition (Rzasa and Ewy 1982;Rice et al 1985;Shimada et al 1986;Koike et al 1988), in some cognitive and adaptative activities (Davis et al 1982;Davis and Pico 1984) and in the activation of some aspects of reproductive behaviour (copulatory behaviour: Kihlström and Dannige 1972;singing behaviour: Voorhuis et al 1991;sexual motivation: Bernroider and Leutgeb 1994).…”

Role of plasma ANG II in the excretion of acute sodium load in a bird with salt glands (Anas platyrhynchos)

“…In addition, centrally applied ANG II stimulates the release of arginine vasotocin, the antidiuretic hormone of birds, as well as stimulating water intake (28). In addition, under conditions of dehydration (19) and hemorrhage (29), plasma ANG II concentrations rise, and during salt loading the levels decrease (15,18), providing further evidence that the physiological function of ANG II is to prevent extracellular fluid volume shrinkage, via antinatriuresis and antidiuresis.…”

Central vasotocin-immunoreactive system in a male passerine bird (Junco hyemalis)

“…In birds, the physiological functions classically attributed to VT are the regulation of water and electrolytic balance (for reviews, see Simon Oppermann et al, 1988;Ramieri and Panzica, 1989) and of blood pressure (Szczepanska-Sadowska et al, 1985). Like VP in mammals, VT in birds is involved in the control of reproduction including oviposition (Rzasa and Ewy, 1982;Rice et al, 1985;Shimada et al, 1986;Koike et al, 1988), male sexual behavior (Kihlström and Danninge, 1972;Bernroider and Leutgeb, 1994;Leutgeb, 1995;Castagna et al, 1998;Goodson and Adkins-Regan, 1999) and aggressive behav-ior (Goodson, 1998a,b;Goodson and Adkins-Regan, 1999), and vocalizations (Voorhuis et al, 1991a;Castagna et al, 1998).…”

Distribution of AVT gene expressing neurons in the prosencephalon of Japanese quail and chicken

“…In birds, AVT is involved in the regulation of water and electrolyte balance (for reviews see Simon-Oppermann et al 1988;Ramieri and Panzica 1989), in thermoregulation (Hassinen et al 1994), in the regulation of blood pressure (SzczepanskaSadowska et al 1985), in oviposition (Rzasa and Ewy 1982;Rice et al 1985;Shimada et al 1986;Koike et al 1988), in some cognitive and adaptative activities (Davis et al 1982;Davis and Pico 1984) and in the activation of some aspects of reproductive behaviour (copulatory behaviour: Kihlström and Dannige 1972;singing behaviour: Voorhuis et al 1991;sexual motivation: Bernroider and Leutgeb 1994).…”